Prof Susan Branford
Centre for Cancer Biology
College of Health
Eligible to supervise Masters and PhD - email supervisor to discuss availability.
Associate Professor Susan BranfordHead, Leukaemia Unit, Molecular and Genetic PathologyQualifications: PhD, University of South Australia, Fellow of the Faculty of Science (RCPA).Susan Branford holds the position of an Associate Professor at the School of Medicine and the School of Molecular and Biomedical Science of Adelaide University in Australia. She has special expertise in molecular monitoring of the BCR-ABL gene for patients with chronic myeloid leukaemia. As such she is a major contributor to international collaborative initiatives to establish guidelines and recommendations for producing reliable molecular data. Associate Professor Branford's main research is focused on the formation of the BCR-ABL gene, the mechanisms of kinase inhibitor drug resistance and the factors that predict for response to therapy and the development of drug resistance.VIDEOS:The importance of Molecular Monitoring in CMLDecember 2011, ICMLfThe importance of BCR-ABL kinase domain mutation analysis in CMLDecember 2011, ICMLfTranscript typing in CML patients April 26, 2010, OncUViewTVTKI therapy for CML April 26, 2010, OncUViewTVImatinib therapy for CML April 23 2010, OncUViewTVInternational reporting scale for CML patients 13 avril 2010, OncUViewTV
| Year | Citation |
|---|---|
| 2025 | Branford, S. (2025). Non-<i>ABL1 </i>Mutations in Newly Diagnosed Patients: Implications. In CLINICAL LYMPHOMA MYELOMA & LEUKEMIA Vol. 25 (pp. S52-S53). CIG MEDIA GROUP, LP. |
| 2024 | Wechalekar, G., Cibich, A., Kutyna, M., Shanmuganathan, N., Sekaran, U. C., Singhal, D., . . . Hiwase, D. (2024). Clonal Architecture of Donor-Derived Leukemia/Clonal Hematopoiesis after Allogeneic Hematopoietic Stem Cell Transplant. In BLOOD Vol. 144 (pp. 4928-4929). FL, Orlando: ELSEVIER. DOI |
| 2024 | Branford, S., Fernandes, A., Wadham, C., Maqsood, M., Shahrin, N. H., Ross, D. M., . . . Shanmuganathan, N. (2024). Longitudinal Clonal Tracking Reveals That Early and Sensitive Detection of Blood Cancer-Related Gene Variants in Patients with Chronic Myeloid Leukemia Predicts Treatment Failure. In BLOOD Vol. 144 (pp. 996-997). FL, Orlando: ELSEVIER. DOI WoS1 |
| 2024 | Shanmuganathan, N., Wadham, C., Yeung, D., Shahrin, N. H., Fernandes, A., Maqsood, M., . . . Branford, S. (2024). Strong Association between Cancer Gene Variants at Diagnosis, Especially<i> ASXL1,</i> and Emergence of Kinase Domain Mutation-Driven Resistance in CML Patients Despite Frontline Treatment with More Potent BCR::ABL1 Inhibitors. In BLOOD Vol. 144 (pp. 992). FL, Orlando: ELSEVIER. DOI WoS5 |
| 2024 | Yeung, D. T., Shanmuganathan, N., Yong, A. S. M., Shortt, J., Chee, L. C. Y., Vialla, N., . . . Hughes, T. P. (2024). Update of the Ascend-CML Study of Frontline Asciminib: High Rate of Optimal Response and Resistance Due to Mutations Is Rare. In BLOOD Vol. 144 (pp. 477-478). FL, Orlando: ELSEVIER. DOI WoS2 |
| 2024 | Pagani, I. S., Krishnan, V., Ouyang, J., Kok, C. H., Chen, B., Page, E. C., . . . Ross, D. M. (2024). Imatinib-Sensitive Chronic Myeloid Leukaemia Is Associated with mtDNA Mutations and Reduced Oxphos Capacity. In BLOOD Vol. 144 (pp. 2715-2716). ELSEVIER. DOI |
| 2023 | Branford, S., Wadham, C., Shanmuganathan, N., Fernandes, A., Shahrin, N. H., Feng, J., . . . Hughes, T. P. (2023). Age-Related Clonal Hematopoiesis Mutations Detected at the Time of Stopping Tyrosine Kinase Inhibitor Therapy Predict the Achievement of Treatment-Free Remission for Patients with CML. In BLOOD Vol. 142 (pp. 5 pages). CA, San Diego: ELSEVIER. DOI WoS5 |
| 2023 | Hong, L. E., Kok, C. H., Kutyna, M., Li, J. J., Chhetri, R., Ross, D. M., . . . Hiwase, D. (2023). High Prevalence of IDH Mutation in Myeloid Neoplasm with Concomitant Autoimmune Rheumatic Disorders. In BLOOD Vol. 142 (pp. 4 pages). CA, San Diego: ELSEVIER. DOI |
| 2023 | Yeung, D. T., Shanmuganathan, N., Reynolds, J., Branford, S., Walia, M., Yong, A. S. M., . . . Hughes, T. P. (2023). Excellent Early and Major Molecular Responses Observed with Asciminib Treatment for CP-CML: Results from the ALLG CML13 Ascend-CML Study. In BLOOD Vol. 142 (pp. 6 pages). CA, San Diego: ELSEVIER. DOI |
| 2023 | Branford, S., Hochhaus, A., Mauro, M., Minami, Y., Rea, D., Boquimpani De Moura Freitas, C. M., . . . Hughes, T. P. (2023). Impact of Mutations in Blood Cancer-Related Genes on Clinical Outcomes in Chronic Myeloid Leukemia in Chronic Phase (CML-CP) after ≥2 Tyrosine Kinase Inhibitors ( TKIs) in the Ascembl Trial. In BLOOD Vol. 142 (pp. 4 pages). CA, San Diego: ELSEVIER. DOI WoS2 |
| 2022 | Hughes, T., Mauro, M., Branford, S., Deng, W., Wang, Q., Collins, H., & Hochhaus, A. (2022). First-in-Human Study of Elvn-001, a Highly Selective BCR::ABL1 Tyrosine Kinase Inhibitor, in Patients with Chronic Myeloid Leukemia Who Failed Previous Tyrosine Kinase Inhibitor Therapies. In BLOOD Vol. 140 (pp. 6780-6781). LA, New Orleans: ELSEVIER. DOI WoS1 |
| 2022 | Shanmuganathan, N., Yeung, D. T., Wadham, C., Shahrin, N. H., Fernandes, A., Feng, J., . . . Branford, S. (2022). Additional Mutational Events at Diagnosis of CML Confer Inferior Failure-Free Survival and Molecular Response for Patients Treated with Frontline Imatinib but Not for Patients Treated with Frontline Second-Generation Tyrosine Kinase Inhibitors. In BLOOD Vol. 140 (pp. 2 pages). LA, New Orleans: ELSEVIER. DOI |
| 2022 | Branford, S., Shanmuganathan, N., Wadham, C., Shahrin, N. H., Fernandes, A., Feng, J., . . . Hughes, T. (2022). Clonal Hematopoiesis Detected at the Time of Tyrosine Kinase Inhibitor Cessation Is Associated with Delayed Molecular Recurrence after Treatment-Free Remission in Patients with CML. In BLOOD Vol. 140 (pp. 3916-3917). LA, New Orleans: ELSEVIER. DOI WoS1 |
| 2022 | Yeung, D. T., Shanmuganathan, N., Reynolds, J., Branford, S., Walia, M., Yong, A. S. M., . . . Hughes, T. (2022). Early and Deep Molecular Responses Achieved with Frontline Asciminib in Chronic Phase CML - Interim Results from ALLG CML13 Ascend-CML. In BLOOD Vol. 140 (pp. 3 pages). LA, New Orleans: ELSEVIER. DOI |
| 2021 | Lu, L., Dang, P., HoowKok, C., Saunders, V. A., Branford, S., P.Hughes, T., & TYeung, D. (2021). Highly Sensitive Droplet Digital PCR to Identify CML Patients with a High Probability of Achieving Treatment-Free Remission. In BLOOD Vol. 138 (pp. 4 pages). GA, Atlanta: ELSEVIER. DOI WoS1 |
| 2020 | Shanmuganathan, N., Wadham, C., Shahrin, N. H., Thomson, D., Feng, J., Saunders, V. A., . . . Branford, S. (2020). Mutated Cancer-Related Genes Detected at Diagnosis of CML and a Novel Class of Variant Associated with the Philadelphia Translocation Are Both Independent Predictors of Inferior Outcomes. In BLOOD Vol. 136 (pp. 4 pages). ELECTR NETWORK: ELSEVIER. DOI WoS4 |
| 2020 | Radich, J., Larson, R., Kantarjian, H., Deininger, M., Pinilla-Ibarz, J., DeAngelo, D., . . . Druker, B. (2020). Exploratory Biomarker Analysis from ENESTnd: Gene Expression Signature Distinguishes Deep Molecular Response (DMR) from Poor Response in Chronic Myeloid Leukemia (CML). In CLINICAL LYMPHOMA MYELOMA & LEUKEMIA Vol. 20 (pp. S233). CIG MEDIA GROUP, LP. |
| 2019 | Shanmuganathan, N., Thomson, D., Wadham, C., Saunders, V. A., Shahrin, N. H., Yeung, D. T., . . . Branford, S. (2019). RNA Splicing Defects in Cancer-Linked Genes Indicate Mutation or Focal Gene Deletion and Are Associated with TKI Resistance in CML. In BLOOD Vol. 134 (pp. 4 pages). Orlando, FL: AMER SOC HEMATOLOGY. DOI WoS1 |
| 2019 | Radich, J. P., Larson, R. A., Kantarjian, H. M., Deininger, M. W., Ibarz, J. P., DeAngelo, D. J., . . . Druker, B. J. (2019). Gene Expression Signature Predicts Deep Molecular Response (DMR) in Chronic Myeloid Leukemia (CML): An Exploratory Biomarker Analysis from ENESTnd. In BLOOD Vol. 134 (pp. 5 pages). Orlando, FL: AMER SOC HEMATOLOGY. DOI WoS2 |
| 2019 | Branford, S., Wadham, C., Shanmuganathan, N., Thomson, D., Shahrin, N. U. R. H., Feng, J., . . . Hughes, T. P. (2019). An RNA-Based Next Generation Sequencing (NGS) Strategy Detects More Cancer Gene Mutations Than a DNA-Based Approach for the Prediction and Assessment of Resistance in CML. In BLOOD Vol. 134 (pp. 4 pages). FL, Orlando: ELSEVIER. DOI |
| 2019 | Branford, S., & Shanmuganathan, N. (2019). NGS in CML - new standard diagnostic procedure?. In HemaSphere Vol. 3 (pp. 48-50). US: Wolters Kluwer Health. DOI Scopus7 WoS8 Europe PMC6 |
| 2019 | Brown, A. L., Babic, M., Schreiber, A., Feng, J., Dobbins, J., Arts, P., . . . Scott, H. S. (2019). Familial Clustering of Hematological Malignancies: Harbingers of Wider Germline Cancer Susceptibility. In BLOOD Vol. 134 (pp. 3 pages). FL, Orlando: ELSEVIER. DOI |
| 2019 | Shahrin, N. H., Thomson, D., Wadham, C., Schreiber, A., & Branford, S. (2019). IMATINIB INDUCES MARKED UPREGULATION OF RECOMBINATION ACTIVATING GENE (RAG) EXPRESSION IN BCR-ABL1 POSITIVE LYMPHOID CELLS. In EXPERIMENTAL HEMATOLOGY Vol. 76 (pp. S85). ELSEVIER SCIENCE INC. |
| 2018 | Shanmuganathan, N., Branford, S., Yong, A., Hiwase, D., Yeung, D., Ross, D., & Hughes, T. (2018). Predictors of Success in Treatment-Free Remission: A Single Centre Experience. In CLINICAL LYMPHOMA MYELOMA & LEUKEMIA Vol. 18 (pp. S224). CIG MEDIA GROUP, LP. DOI |
| 2018 | Yeung, D. T., Grigg, A. P., Shanmuganathan, N., Cunningham, I., Shortt, J., Rowling, P., . . . Hughes, T. P. (2018). Combination of Nilotinib and Pegylated Interferon Alfa-2b Results in High Molecular Response Rates in Chronic Phase CML: Interim Results of the ALLG CML 11 Pinnacle Study. In BLOOD Vol. 132 (pp. 5 pages). San Diego, CA: AMER SOC HEMATOLOGY. DOI WoS7 |
| 2018 | Thomson, D., Shahrin, H., Wang, P., Wadham, C., Hughes, T. P., Schreiber, A., & Branford, S. (2018). High Recombination Activating Gene (RAG) Expression and RAG Mediated Recombination Is Associated with Oncogenic Rearrangement Observed with Tyrosine Kinase Inhibitor Resistant CML. In BLOOD Vol. 132 (pp. 4 pages). CA, San Diego: AMER SOC HEMATOLOGY. DOI WoS2 |
| 2017 | Branford, S., Wang, P., Yeung, D., Purins, A., Marum, J. E., Nataren, N., . . . Hughes, T. P. (2017). Integrative Genomics Reveals Cancer Associated Mutations Are Common at Diagnosis of CML in Patients with Poor Response to TKI Therapy. In BLOOD Vol. 130 (pp. 4 pages). Atlanta, GA: AMER SOC HEMATOLOGY. |
| 2017 | Shanmuganathan, N., Branford, S., Yeung, D., Hiwase, D. K., Yong, A. S. M., Ross, D. M., & Hughes, T. P. (2017). Cumulative Incidence of Treatment-Free Remission (TFR) for Patients with Chronic Myeloid Leukemia (CML): The Adelaide Experience. In BLOOD Vol. 130 (pp. 3 pages). Atlanta, GA: AMER SOC HEMATOLOGY. |
| 2017 | Ross, D. M., Pagani, I. S., Shanmuganathan, N., Seymour, J. F., Mills, A. K., Filshie, R. J., . . . Hughes, T. P. (2017). Long-term Follow-up of the ALLG CML8 TWISTER Study of Treatment-free Remission (TFR) in Patients With Chronic Myeloid Leukemia (CML).. In Blood Vol. 130 (pp. 1597). Atlanta: American Society of Hematology. |
| 2017 | Pagani, I., Dang, P., Kommers, I., Goyne, J., Saunders, V., Prime, J., . . . Ross, D. (2017). Comparison of genomic and reverse transcriptase Q-PCR for the monitoring of first-line imatinib treatment: an ALLG CML9 sub-study. In Haematologica. Madrid: Ferrata Storti Foundation. |
| 2016 | Marum, J. E., Wang, P. P. S., Stangl, D., Yeung, D. T., Mueller, M. C., Dietz, C. T., . . . Branford, S. (2016). Novel Fusion Genes at CML Diagnosis Reveal a Complex Pattern of Genomic Rearrangements and Sequence Inversions Associated with the Philadelphia Chromosome in Patients with Early Blast Crisis. In BLOOD Vol. 128 (pp. 6 pages). CA, San Diego: AMER SOC HEMATOLOGY. DOI WoS2 |
| 2016 | Shanmuganathan, N., Branford, S., Braley, J., Hiwase, D., Yeung, D. T., Ross, D. M., & Hughes, T. P. (2016). For Patients with Sustained MR4-MR4.5, Less Frequent Molecular Monitoring during the First 12 Months after Tyrosine Kinase Inhibitor Cessation Is Viable for Timely Detection of Loss of MMR. In BLOOD Vol. 128 (pp. 7 pages). CA, San Diego: AMER SOC HEMATOLOGY. DOI |
| 2016 | Yeung, D. T., Osborn, M. P., White, D. L., Branford, S., Gerber, T., Butcher, B., . . . Hughes, T. P. (2016). Upfront Imatinib with Selective Early Switching to Nilotinib Leads to Excellent Achievement of Deep Molecular Response in Chronic Phase CML: 5 Year (Final) Analysis of the TIDEL-II Study. In BLOOD Vol. 128 (pp. 6 pages). San Diego, CA: AMER SOC HEMATOLOGY. DOI |
| 2016 | Hiwase, D. K., Tan, P., D'Rozario, J., Taper, J., Powell, A. R., Irving, I., . . . Hughes, T. P. (2016). Efficacy and Safety of Nilotinib 300 Mg Twice Daily (BD) in Patients with CML in Chronic Phase (CML-CP) Who Are Intolerant to Prior BCR-ABL Tyrosine Kinase Inhibitors (TKIs): Results from the Randomized, Phase IIIb ENES Tswift Study. In BLOOD Vol. 128 (pp. 6 pages). CA, San Diego: AMER SOC HEMATOLOGY. DOI |
| 2016 | Wang, P., Parker, W., Branford, S., & Schreiber, A. (2016). BAM-matcher: a tool for rapid NGS sample matching. In Bioinformatics Vol. 32 (pp. 2699-2701). UK: Oxford University Press. DOI Scopus34 WoS32 Europe PMC35 |
| 2015 | Hughes, T. P., Cervantes, F., Leber, B., Spector, N., Lipton, J. H., Pasquini, R., . . . Branford, S. (2015). ENESTCMR 4-Y RESULTS: PATIENTS (PTS) WITH CHRONIC MYELOID LEUKEMIA IN CHRONIC PHASE (CML-CP) AND RESIDUAL DISEASE MORE LIKELY TO ACHIEVE DEEP MOLECULAR RESPONSE FOLLOWING SWITCH TO NILOTINIB (NIL). In HAEMATOLOGICA Vol. 100 (pp. 61-62). Vienna, AUSTRIA: FERRATA STORTI FOUNDATION. |
| 2015 | Hughes, T. P., Cervantes, F., Spector, N., Leber, B., Branford, S., Glynos, T. A., . . . Lipton, J. H. (2015). Treatment-Free Remission (TFR) Eligibility in Patients (pts) with Chronic Myeloid Leukemia in Chronic Phase (CML-CP) and Residual Disease on Long-Term Imatinib (IM) Who Switched to Second-Line Nilotinib (NIL). In BLOOD Vol. 126 (pp. 4 pages). Orlando, FL: AMER SOC HEMATOLOGY. |
| 2015 | Eadie, L. N., Saunders, V. A., Leclercq, T. M., Branford, S., White, D. L., & Hughes, T. P. (2015). The Allosteric Inhibitor ABL001 Is Susceptible to Resistance in Vitro Mediated By Overexpression of the Drug Efflux Transporters ABCB1 and ABCG2. In BLOOD Vol. 126 (pp. 3 pages). Orlando, FL: AMER SOC HEMATOLOGY. |
| 2015 | Yeung, D. T., Parker, W. T., Phillis, S., Georgievski, J., Scott, H. S., Hughes, T. P., & Branford, S. (2015). BCR-ABL Assay Sensitivity of MR4.5 Achieved in >90%, and MR5 in >75% of Samples, through mRNA Selection before qRT-PCR. In BLOOD Vol. 126 (pp. 3 pages). Orlando, FL: AMER SOC HEMATOLOGY. |
| 2015 | Hahn, C. N., Babic, M., Schreiber, A. W., Kutyna, M. M., Wee, L. A., Brown, A. L., . . . Hiwase, D. (2015). Rare and Common Germline Variants Contribute to Occurrence of Myelodysplastic Syndrome. In BLOOD Vol. 126 (pp. 4 pages). Orlando, FL: AMER SOC HEMATOLOGY. DOI WoS3 |
| 2015 | Marum, J. E., Purins, L., Yeung, D. T., Parker, W. T., Price, D. J., Wang, P. P. S., . . . Branford, S. (2015). Germline Genetic Variation of ASXL1 and BIM Predicts Response to Imatinib and Identifies a Subset of High Sokal Risk Patients with the Greatest Risk of Treatment Failure and Disease Progression. In BLOOD Vol. 126 (pp. 4 pages). Orlando, FL: AMER SOC HEMATOLOGY. DOI |
| 2015 | Branford, S., Wang, P. P. S., Parker, W. T., Yeung, D., Marum, J. E., Stangl, D., . . . Hughes, T. P. (2015). High Incidence of Mutated Cancer-Associated Genes at Diagnosis in CML Patients with Early Transformation to Blast Crisis. In BLOOD Vol. 126 (pp. 4 pages). Orlando, FL: AMER SOC HEMATOLOGY. |
| 2015 | Smith, C. C., Paguirigan, A., Chin, C. -S., Brown, M., Parker, W., Levis, M. J., . . . Shah, N. P. (2015). Polyclonal and heterogeneous resistance to targeted therapy in leukemia. In CANCER RESEARCH Vol. 75 (pp. 3 pages). Philadelphia, PA: AMER ASSOC CANCER RESEARCH. DOI |
| 2014 | Matsumura, I., Nakamae, H., Yoshida, C., Fletcher, L., Branford, S., Koga, D., . . . Naoe, T. (2014). Odk-1201, One-Step RT-qPCR Major <i>BCR-ABL/ABL</i> mRNA Kit for the International Scale, with High Sensitivity to Detect Deeper MR. In BLOOD Vol. 124 (pp. 3 pages). San Francisco, CA: AMER SOC HEMATOLOGY. |
| 2014 | Magistroni, V., Piazza, R., Sharma, N., Parker, W., Pirola, A., Yeung, D., . . . Gambacorti-Passerini, C. (2014). IDENTIFICATION OF RECURRENT GENETIC ALTERATIONS ASSOCIATED WITH BLAST CRISIS TRANSFORMATION IN CHRONIC MYELOID LEUKEMIA. In HAEMATOLOGICA Vol. 99 (pp. 510-511). Milan, ITALY: FERRATA STORTI FOUNDATION. |
| 2014 | Deininger, M. W., Shah, N. P., Cortes, J. E., Kim, D. W., Nicolini, F. E., Talpaz, M., . . . Branford, S. (2014). LONGER-TERM FOLLOW-UP OF THE IMPACT OF BASELINE (BL) MUTATIONS ON PONATINIB RESPONSE AND END OF TREATMENT (EOT) MUTATION ANALYSIS IN PATIENTS (PTS) WITH CHRONIC PHASE CHRONIC MYELOID LEUKEMIA (CP-CML). In HAEMATOLOGICA Vol. 99 (pp. 533). Milan, ITALY: FERRATA STORTI FOUNDATION. |
| 2014 | Branford, S., Kamel-Reid, S., Bendit, I., Etienne, G., Guerci-Bresler, A., Hughes, T. P., . . . Cervantes, F. (2014). EARLY MOLECULAR RESPONSE PREDICTS ACHIEVEMENT OF UNDETECTABLE BCR-ABL IN PATIENTS (PTS) WITH CHRONIC MYELOID LEUKEMIA IN CHRONIC PHASE (CML-CP) TREATED WITH NILOTINIB: 3-YEAR FOLLOW-UP OF ENESTCMR. In HAEMATOLOGICA Vol. 99 (pp. 532). Milan, ITALY: FERRATA STORTI FOUNDATION. WoS3 |
| 2013 | Branford, S., Roberts, N., Yeung, D. T., Altamura, H., Parker, W. T., & Hughes, T. P. (2013). Any BCR-ABL Reduction Below 10% At 6 Months Of Therapy Significantly Improves Outcome For CML Patients With a Poor Response At 3 Months. In BLOOD Vol. 122 (pp. 2 pages). New Orleans, LA: AMER SOC HEMATOLOGY. WoS9 |
| 2012 | Ross, M., Branford, S., Seymour, J., Arthur, C., Schwarer, A., Dang, P., . . . Hughes, T. (2012). FREQUENT AND SUSTAINED DRUG-FREE REMISSION IN THE AUSTRALASIAN CML8 TRIAL OF IMATINIB WITHDRAWAL. In HAEMATOLOGICA Vol. 97 (pp. 74-75). FERRATA STORTI FOUNDATION. WoS2 |
| 2012 | Morley, A., Bartley, P., Latham, S., Budgen, B., Ross, D., Hughes, E., . . . Hughes, T. (2012). DNA-qPCR vs RT-qPCR for Monitoring MRD in Chronic Myeloid Leukemia. In JOURNAL OF MOLECULAR DIAGNOSTICS Vol. 14 (pp. 662-663). Long Beach, CA: ELSEVIER SCIENCE INC. |
| 2012 | Smith, C. C., Brown, M., Parker, W. T., Lin, K., Travers, K., Wang, S., . . . Shah, N. (2012). Single Molecule Real Time (SMRT™) Sequencing Sensitively Detects the Evolution of Polyclonal and Compound BCR-ABL Mutations in Patients Who Relapse On Kinase Inhibitor Therapy. In BLOOD Vol. 120 (pp. 2 pages). GA, Atlanta: AMER SOC HEMATOLOGY. DOI WoS9 |
| 2011 | Hughes, T. P., Lipton, J. H., Leber, B., Spector, N., Cervantes, F., Pasquini, R., . . . Branford, S. (2011). Complete Molecular Response (CMR) Rate with Nilotinib in Patients (pts) with Chronic Myeloid Leukemia in Chronic Phase (CML-CP) without CMR, After ≥ 2 Years on Imatinib: Preliminary Results From the Randomized ENESTcmr Trial of Nilotinib 400 Mg Twice Daily (BID) Vs Imatinib. In BLOOD Vol. 118 (pp. 278). San Diego, CA: AMER SOC HEMATOLOGY. WoS1 |
| 2011 | Yeung, D. T., Osborn, M., White, D. L., Branford, S., Kornhauser, M., Slader, C., . . . Hughes, T. P. (2011). Upfront Imatinib Therapy in CML Patients with Rapid Switching to Nilotinib for Failure to Achieve Molecular Targets or Intolerance Achieves High Overall Rates of Molecular Response and a Low Risk of Progression - An Update of the TIDEL-II Trial. In BLOOD Vol. 118 (pp. 208). San Diego, CA: AMER SOC HEMATOLOGY. WoS1 |
| 2011 | le Coutre, P. D., Giles, F. J., Pinilla-Ibarz, J., Larson, R. A., Gattermann, N., Ottmann, O. G., . . . Kantarjian, H. M. (2011). Nilotinib in Imatinib-Resistant or -Intolerant Patients (pts) with Chronic Myeloid Leukemia in Chronic Phase (CML-CP): 48-Month Follow-up Results of a Phase 2 Study. In BLOOD Vol. 118 (pp. 1610). San Diego, CA: AMER SOC HEMATOLOGY. WoS1 |
| 2011 | Branford, S., Yeung, D. T., Prime, J., Ross, D., & Hughes, T. P. (2011). Imatinib Dose Interruption in Responding CML Patients Is Associated with Characteristic BCR-ABL Kinetics, Which Could Help to Differentiate Non-Adherence From Drug Resistance. In BLOOD Vol. 118 (pp. 55). San Diego, CA: AMER SOC HEMATOLOGY. WoS1 |
| 2011 | Parker, W. T., Ho, M., Scott, H. S., Hughes, T. P., & Branford, S. (2011). Multiple Low Level Mutations Identifies Imatinib Resistant CML Patients At Risk of Poor Response to Second-Line Inhibitor Therapy, Irrespective of the Resistance Profile of the Mutations. In BLOOD Vol. 118 (pp. 54). San Diego, CA: AMER SOC HEMATOLOGY. WoS1 |
| 2010 | White, E., Matejtschuk, P., Rigsby, P., Gabert, J., Wang, Y., Branford, S., . . . Cross, N. (2010). ESTABLISHMENT OF THE 1ST WORLD HEALTH ORGANIZATION INTERNATIONAL GENETIC REFERENCE PANEL FOR QUANTITATION OF BCR-ABL MRNA. In HAEMATOLOGICA Vol. 95 (pp. 84-85). Barcelona, SPAIN: FERRATA STORTI FOUNDATION. |
| 2010 | Yeung, D. T., Osborn, M., White, D. L., Branford, S., Haswell, L., Slader, C., . . . Hughes, T. (2010). Selective Escalation of Imatinib Therapy and Early Switching to Nilotinib In De Novo Chronic Phase CML Patients: Interim Results From the TIDEL-II Trial. In BLOOD Vol. 116 (pp. 96). Orlando, FL: AMER SOC HEMATOLOGY. DOI WoS10 |
| 2010 | Parker, W., Ho, M., Lawrence, R., Irwin, D., Scott, H., Hughes, T., & Branford, S. (2010). Detection of low level nilotinib or dasatinib resistant BCR-ABL mutations by mass spectrometry in CML patients who fail Imatinib is highly predivtive of their subsequent clonal expansion when treated with the drug for which their mutation confers resistance. In Proceedings of 2010 american society of hematology meeting Vol. 116 (pp. 0 pages). Florida, USA: AMER SOC HEMATOLOGY. |
| 2010 | Prime, H., Romeo, G., Phillis, S., Field, C., Jamison, B., Prime, J., . . . Branford, S. (2010). Contrasting response of patients with chronic myeloid leukaemia (CML) and the highly imatinib resistant L248V mutation that may be related to an increased propensity of some patients to form an associated deletion mutant with increased imatinib sensitivity. In Proceedings of Haematology association of australasia annual meeting (pp. 0 pages). Auckland, New Zealand. |
| 2010 | Branford, S., Goh, H., Izzo, B., Beppu, L., Ortmann, C., Duniec, K., . . . Hughes, T. (2010). A Review of Mutation Analysis In the TOPS Trial of Standard Dose Versus High Dose IM In CML Suggests That Refinements to the ELN Recommendations for Mutation Screening May Be Appropriate. In Proceedings of 52nd American Society of Hematology Meeting (ASH), as published in Blood Vol. 116 (pp. 389-390). Washington, DC: American Society of Hematology. WoS1 |
| 2010 | Fletcher, L., Prime, J., Phillis, S., Jamison, B., Field, C., Prime, H., . . . Branford, S. (2010). Limiting the variability within a BCR-ABL quantitative PCR (RQ-PCR) assay is essential for optimal concordance of results between laboratories generating BCR-ABL values on an international reporting scale. In Proceedings of Haematology association of australasia annual meeting (pp. 0 pages). New Zealand. |
| 2010 | Branford, S., Martinelli, G., Saglio, G., Kim, D., Shou, Y., Reynolds, J., . . . Radich, J. (2010). Association of early molecular response to nilotinib with probability of cytogenetic response in chronic myeloid leukemia patients (pts) who fail imatinib. In Proceedings of American society of clinical oncology conference Vol. 28 (pp. 0 pages). AMER SOC CLINICAL ONCOLOGY. DOI WoS2 |
| 2010 | Morley, A., Bartley, P., Ross, D., Latham, S., Budgen, B., Branford, S., & Hughes, T. (2010). Towards DNA-based monitoring of therapy in chronic myeloid leukemia. In Proceedings of 2010 American society of hematology meeting Vol. 116 (pp. 0 pages). Orlando, FL: AMER SOC HEMATOLOGY. |
| 2010 | Kim, D., Kim, D., Kim, S., Goh, H., Pane, F., Hughes, T., . . . Hochhaus, A. (2010). Mutation analysis of BCR-ABL tyrosine kinase domain in new chronic phase-chronic myeloid leukemia patients with suboptimal response or treatment failure from imatinib treatment. In Proceedings of 2010 American society of hematology meeting Vol. 116 (pp. 0 pages). Orlando, FL: AMER SOC HEMATOLOGY. |
| 2010 | Yeung, D., Osborn, M., White, D., Branford, S., Haswell, L., Slader, C., . . . Hughes, T. (2010). Selective escalation of imatinib therapy and early switching to nilotinib in de novo chronic phase CML patients: interim results from the TIDELL-II trial. In Proceedings of 2010 American Society of Hematology conference (pp. 1-2). Florida. |
| 2010 | Saglio, S., Hughes, T., Kim, D., Hanfstein, B., Gottardi, E., Branford, S., . . . Martinelli, G. (2010). RESPONSE TO NILOTINIB IN PATIENTS WITH IMATINIB-RESISTANT OR -INTOLERANT CHRONIC MYELOID LEUKEMIA IN CHRONIC PHASE (CML-CP) WITH DIFFERENT BCR-ABL TRANSCRIPT TYPES. In HAEMATOLOGICA Vol. 95 (pp. 342-343). FERRATA STORTI FOUNDATION. |
| 2010 | Martinelli, G., Hochhaus, A., Radich, J., Soverini, S., Branford, S., Erben, P., . . . Kim, D. (2010). DETECTION OF NEW MUTATIONS IN NILOTINIB-TREATED PATIENTS WITH IMATINIB-RESISTANT CHRONIC MYELOID LEUKEMIA IN CHRONIC PHASE. In HAEMATOLOGICA Vol. 95 (pp. 62). Barcelona, SPAIN: FERRATA STORTI FOUNDATION. |
| 2010 | Morley, A., Bartley, P., Ross, D., Latham, S., Budgen, B., Hughes, E., . . . Hughes, T. (2010). Monitoring of CML by DNA qPCR. In JOURNAL OF MOLECULAR DIAGNOSTICS Vol. 12 (pp. 868). San Jose, CA: AMER SOC INVESTIGATIVE PATHOLOGY, INC. |
| 2010 | Stein, A., Shou, Y., Bottino, D., Chia, Y., Woodman, R., Martinelli, G., . . . Radich, J. (2010). RAPID INITIAL DECLINE IN BCR-ABL LEVELS IS ASSOCIATED WITH SUPERIOR RESPONSES IN IMATINIB-RESISTANT OR -INTOLERANT CHRONIC MYELOID LEUKEMIA PATIENTS IN CHRONIC PHASE (CML-CP) TREATED WITH NILOTINIB. In HAEMATOLOGICA Vol. 95 (pp. 56). Barcelona, SPAIN: FERRATA STORTI FOUNDATION. |
| 2010 | Hughes, T., Kim, D., Martinelli, G., Branford, S., Mueller, M., Beppu, L., . . . Hochhaus, A. (2010). EARLY MOLECULAR RESPONSE TO NILOTINIB IN PATIENTS WHO FAILED IMATINIB IS ASSOCIATED WITH A HIGHER PROBABILITY OF CYTOGENETIC RESPONSE IN CHRONIC MYELOID LEUKEMIA (CML). In HAEMATOLOGICA Vol. 95 (pp. 54). Barcelona, SPAIN: FERRATA STORTI FOUNDATION. WoS1 |
| 2010 | Kim, D., Kim, S., Goh, H., Pane, F., Hughes, T., Radich, J., . . . Kim, D. (2010). BCR-ABL MUTATION ANALYSIS USING BOTH ASO-PCR AND DIRECT SEQUENCING IN NEW CHRONIC PHASE CHRONIC MYELOID LEUKEMIA PATIENTS WITH SUBOPTIMAL RESPONSE OR TREATMENT FAILURE FROM IMATINIB TREATMENT. In HAEMATOLOGICA Vol. 95 (pp. 344-345). FERRATA STORTI FOUNDATION. |
| 2009 | Saglio, G., Hochhaus, A., Martinelli, G., Gottardi, E., Soverini, S., Branford, S., . . . Kim, D. (2009). DYNAMICS OF CYTOGENETIC AND MOLECULAR RESPONSE TO NILOTINIB IS SIMILAR IN IMATINIB-RESISTANT CHRONIC MYELOID LEUKEMIA PATIENTS IN CHRONIC PHASE (CML-CP) WITH AND WITHOUT BCR-ABL MUTATIONS EXCEPT E255K/V, Y253H, AND F359C/V. In HAEMATOLOGICA Vol. 94 (pp. 261). Berlin, GERMANY: FERRATA STORTI FOUNDATION. |
| 2009 | Mueller, M. C., Cross, N. C. P., Erben, P., Schenk, T., Ernst, T., Hehlmann, R., . . . Hochhaus, A. (2009). Harmonization of Molecular Monitoring of CML Therapy in Europe - Perspective of Widespread Competence in <i>BCR</i>-<i>ABL</i> Quantification.. In BLOOD Vol. 114 (pp. 1026). New Orleans, LA: AMER SOC HEMATOLOGY. WoS1 |
| 2009 | Martinelli, G., Kim, D. W., Saglio, G., Branford, S., Erben, P., Gottardi, E., . . . Radich, J. (2009). RESPONSE TO NILOTINIB IS SIMILAR IN IMATINIB-RESISTANT CHRONIC MYELOID LEUKEMIA PATIENTS IN ACCELERATED PHASE (CML-AP) WITH AND WITHOUT BCR-ABL MUTATIONS EXCEPT E25SK/V, Y253H, AND F359C/V. In HAEMATOLOGICA-THE HEMATOLOGY JOURNAL Vol. 94 (pp. 258-259). Berlin, GERMANY: FERRATA STORTI FOUNDATION. WoS1 |
| 2009 | Martinelli, G., Kim, D., Saglio, G., Branford, S., Erben, P., Gottardi, E., . . . Radich, J. (2009). RESPONSE TO NILOTINIB IS SIMILAR IN IMATINIB-RESISTANT CHRONIC MYELOID LEUKEMIA PATIENTS IN ACCELERATED PHASE (CML-AP) WITH AND WITHOUT BCR-ABL MUTATIONS EXCEPT E255K/V, Y253H, AND F359C/V. In HAEMATOLOGICA Vol. 94 (pp. 258-259). FERRATA STORTI FOUNDATION. WoS1 |
| 2009 | Baccarani, M., Druker, B. J., Cortes-Franco, J., Hughes, T. P., Kim, D. -W., Pane, F., . . . Guilhot, F. (2009). 24 Months Update of the TOPS Study: a Phase III, Randomized, Open-Label Study of 400mg/d (SD-IM) Versus 800mg/d (HD-IM) of Imatinib Mesylate (IM) in Patients (Pts) with Newly Diagnosed, Previously Untreated Chronic Myeloid Leukemia in Chronic Phase (CML-CP). In BLOOD Vol. 114 (pp. 142-143). New Orleans, LA: AMER SOC HEMATOLOGY. WoS12 |
| 2009 | Osborn, M. P., Branford, S., White, D. L., Seymour, J. F., Columbus, R., Taylor, K., . . . Hughes, T. P. (2009). Maintaining Imatinib ≥600 Mg Daily in the First 12 Months of Chronic Phase CML Treatment Is Associated with Superior Event-Free Survival at 5 Years.. In BLOOD Vol. 114 (pp. 461-462). New Orleans, LA: AMER SOC HEMATOLOGY. |
| 2009 | Esposito, N., Quintarelli, C., Colavita, I., Izzo, B., Peluso, A. L., Ruoppolo, M., . . . Pane, F. (2009). Reduced Expression Level of SHP1 Gives An Additive Survival Advantage to the Ph plus Cells of Chronic Myeloid Leukemia (CML) Patients and Provides a Novel Pretreatment Predictor of Major Molecular Response Achievement in CML Patients. In BLOOD Vol. 114 (pp. 871-872). New Orleans, LA: AMER SOC HEMATOLOGY. |
| 2009 | Radich, J. P., Martinelli, G., Hochhaus, A., Gottardi, E., Soverini, S., Branford, S., . . . Saglio, G. (2009). Response and Outcomes to Nilotinib at 24 Months in Imatinib-Resistant Chronic Myeloid Leukemia Patients in Chronic Phase (CML-CP) and Accelerated Phase (CML-AP) with and without BCR-ABL Mutations.. In BLOOD Vol. 114 (pp. 464-465). New Orleans, LA: AMER SOC HEMATOLOGY. WoS1 |
| 2009 | Osborn, M. P., White, D. L., Saunders, V. A., Cambareri, B., Branford, S., Menelaou, A., . . . Hughes, T. P. (2009). Early Dose-Escalation in Chronic Myeloid Leukaemia Patients with Low Plasma Imatinib Levels Leads to Equivalent BCR-ABL Values and Drug Levels at 6 Months to Those with Optimal Drug Levels: First Analysis From the TIDEL II Trial of De-Novo Patients Treated with 600mg Imatinib.. In BLOOD Vol. 114 (pp. 465). New Orleans, LA: AMER SOC HEMATOLOGY. |
| 2009 | Branford, S., Hochhaus, A., Mueller, M., Bahceci, E., Ploughman, L., Mukhopadhyay, J., & Hughes, T. (2009). Analysis of Molecular Data and the Emergence of Mutations for Chronic-Phase Chronic Myelogenous Leukemia (CML-CP) Patients Treated with Dasatinib After Imatinib Failure.. In BLOOD Vol. 114 (pp. 1270-1271). New Orleans, LA: AMER SOC HEMATOLOGY. |
| 2009 | Branford, S., Kim, D. -W., Soverini, S., Gottardi, E., Beppu, L., Mueller, M. C., . . . Hochhaus, A. (2009). Molecular Response at 3 Months On Nilotinib Therapy Predicts Response and Long-Term Outcomes in Patients with Imatinib-Resistant or -Intolerant Chronic Myeloid Leukemia in Chronic Phase (CML-CP). In BLOOD Vol. 114 (pp. 1275-1276). New Orleans, LA: AMER SOC HEMATOLOGY. WoS1 |
| 2008 | Branford, S., Lawrence, R., Grigg, A., Seymour, J. F., Schwarerl, A., Arthur, C., . . . Hughes, T. (2008). Long Term Follow up of Patients with CML in Chronic Phase Treated with First-Line Imatinib Suggests That Earlier Achievement of a Major Molecular Response Leads to Greater Stability of Response. In BLOOD Vol. 112 (pp. 735-736). San Francisco, CA: AMER SOC HEMATOLOGY. WoS3 |
| 2008 | Esposito, N., Quarantelli, F., Luciano, L., Izzo, B., Peluso, A. L., Picardi, M., . . . Pane, F. (2008). The Expression of shp-1 and SHP-2: A Novel Powerful Predictor of Major Molecular Response (MMR) Achievement in Chronic Myeloid Leukemia Gleevec-Treated Patients Enrolled into the TOPS Clinical Trial. In BLOOD Vol. 112 (pp. 404). San Francisco, CA: AMER SOC HEMATOLOGY. |
| 2008 | Hughes, T. P., Hochhaus, A., Branford, S., Mueller, M. C., Foroni, L., Druker, B. J., . . . Goldman, J. M. (2008). Reduction of BCR-ABL Transcript Levels at 6, 12, and 18 Months (mo) Correlates with Long-Term Outcomes on Imatinib (IM) at 72 Mo: An Analysis from the International Randomized Study of Interferon versus STI571 (IRIS) in Patients (pts) with Chronic Phase Chronic Myeloid Leukemia (CML-CP). In BLOOD Vol. 112 (pp. 129-130). San Francisco, CA: AMER SOC HEMATOLOGY. WoS11 |
| 2008 | Hochhaus, A., Kim, D. -W., Martinelli, G., Hughes, T. P., Soverini, S., Branford, S., . . . Radich, J. P. (2008). Nilotinib Efficacy According to Baseline BCR-ABL Mutations in Patients with Imatinib-Resistant Chronic Myeloid Leukemia in Chronic Phase (CML-CP). In BLOOD Vol. 112 (pp. 1103-1104). San Francisco, CA: AMER SOC HEMATOLOGY. WoS2 |
| 2008 | Hochhaus, A., Mueller, M. C., Radich, J., Branford, S., Hanfstein, B., Rousselot, P., . . . Hughes, T. P. (2008). Dasatinib-Associated Major Molecular Responses Are Rapidly Achieved in Patients with Chronic Myeloid Leukemia in Chronic Phase (CML-CP) Following Resistance, Suboptimal Response, or Intolerance on Imatinib. In BLOOD Vol. 112 (pp. 400). San Francisco, CA: AMER SOC HEMATOLOGY. WoS4 |
| 2008 | Cortes, J., Baccarani, M., Guilhot, F., Druker, B. J., Branford, S., Kim, D. -W., . . . Hughes, T. P. (2008). A Phase III, Randomized. Open-Label Study of 400 Mg Versus 800 Mg of Imatinib Mesylate (1M) in Patients (pts) with Newly Diagnosed, Previously Untreated Chronic Myeloid Leukemia in Chronic Phase (CML-CP) Using Molecular Endpoints: 1-Year Results of TOPS (Tyrosine Kinase Inhibitor Optimization and Selectivity) Study. In BLOOD Vol. 112 (pp. 130-131). San Francisco, CA: AMER SOC HEMATOLOGY. WoS14 |
| 2008 | Cross, C., Hochhaus, A., Mueller, M., Saglio, G., Branford, S., Hughes, T., . . . White, H. (2008). DEVELOPMENT OF PROTOTYPE REFERENCE MATERIALS FOR BCR-ABL QUANTITATIVE RT-PCR. In HAEMATOLOGICA Vol. 93 (pp. 54). Copenhagen, DENMARK: FERRATA STORTI FOUNDATION. |
| 2008 | Zhang, T., Nwachukwu, B., Grenier, S., Wei, C., Branford, S., & Kamel-Reid, S. (2008). Assessment of Quality Controls and Establishment of a Conversion Factor for Monitoring BCR-ABL1 Transcripts in CML. In JOURNAL OF MOLECULAR DIAGNOSTICS Vol. 10 (pp. 583). Grapevine, TX: ELSEVIER SCIENCE INC. |
| 2008 | Morley, A. A., Bartley, P., Ross, D. M., Latham, S., Martin-Harris, H., Budgen, B., . . . Hughes, T. (2008). DNA-Based Monitoring of Minimal Residual Disease(MRD) in Chronic Myeloid Leukemia(CML). In BLOOD Vol. 112 (pp. 406). San Francisco, CA: AMER SOC HEMATOLOGY. |
| 2008 | Ross, D. M., Grigg, A., Schwarer, A., Arthur, C., Loftus, K., Mills, A. K., . . . Hughes, T. (2008). The Majority of Chronic Myeloid Leukaemia Patients Who Cease Imatinib after Achieving a Sustained Complete Molecular Response (CMR) Remain in CMR, and Any Relapses Occur Early. In BLOOD Vol. 112 (pp. 402-403). San Francisco, CA: AMER SOC HEMATOLOGY. WoS10 |
| 2008 | Mueller, M., Erben, P., Saglio, G., Branford, S., Hanfstein, B., Gosenca, D., . . . Hochhaus, A. (2008). EUROPEAN STANDARDIZATION OF BCR-ABL MRNA QUANTIFICATION. In HAEMATOLOGICA Vol. 93 (pp. 61). Copenhagen, DENMARK: FERRATA STORTI FOUNDATION. |
| 2008 | Branford, S., Lawrence, R., Fletcher, L., Field, C., Rudzki, Z., & Hughes, T. (2008). The Initial Molecular Response of Chronic Phase CML Patients Treated with Second Generation ABL Inhibitor Therapy after Imatinib Failure Can Predict Inadequate Response and Provide Indications for Rational Mutation Screening. In BLOOD Vol. 112 (pp. 128). San Francisco, CA: AMER SOC HEMATOLOGY. WoS2 |
| 2008 | Radich, J., Kim, D. -W., Martinelli, G., Soverini, S., Branford, S., Mueller, M., . . . Saglio, G. (2008). RESPONSE TO NILOTINIB IN CHRONIC MYELOGENOUS LEUKEMIA PATIENTS IN CHRONIC PHASE (CML-CP) ACCORDING TO BCR-ABL MUTATIONS AT BASELINE. In HAEMATOLOGICA Vol. 93 (pp. 55). Copenhagen, DENMARK: FERRATA STORTI FOUNDATION. WoS3 |
| 2008 | Usuki, K., Urabe, A., Tojo, A., Maeda, Y., Kobayashi, Y., Jinnai, I., . . . Naoe, T. (2008). A PHASE I/II STUDY OF NILOTINIB IN JAPANESE PATIENTS WITH IMATINIB-RESISTANT OR -INTOLERANT PH+ CHRONIC MYELOGENOUS LEUKEMIA (CML) OR RELAPSED/REFRACTORY PH+ ACUTE LYMPHOBLASTIC LEUKEMIA (ALL). In HAEMATOLOGICA Vol. 93 (pp. 433-434). Copenhagen, DENMARK: FERRATA STORTI FOUNDATION. |
| 2007 | Mueller, M. C., Branford, S., Radich, J., Shah, N., Erben, P., Ernst, T., . . . Hochhaus, A. (2007). Efficacy of dasatinib in chronic phase chronic myelogenous leukemia patients after imatinib failure according to baseline BCR-ABL mutations. In HAEMATOLOGICA-THE HEMATOLOGY JOURNAL Vol. 92 (pp. 127). Vienna, AUSTRIA: FERRATA STORTI FOUNDATION. WoS4 |
| 2007 | Soverini, S., Saglio, G., Branford, S., Radich, J., Kim, D. W., Hughes, T., . . . Martinelli, G. (2007). In patients with chronic myelogeneous leukemia (CML), response dynamics to nilotinibafter imatinib failure depend on thetype of BCR-ABL mutations. In HAEMATOLOGICA-THE HEMATOLOGY JOURNAL Vol. 92 (pp. 320). Vienna, AUSTRIA: FERRATA STORTI FOUNDATION. WoS1 |
| 2007 | Ross, D., Bartley, P. A., Morley, A. A., Seymour, J. F., Branford, S., & Hughes, T. P. (2007). Detection of patient-specific BCR-ABL genomic dna in cml patients with no detectable BCR-ABL by quantitative reverse transcriptase PCR. In HAEMATOLOGICA-THE HEMATOLOGY JOURNAL Vol. 92 (pp. 212). Vienna, AUSTRIA: FERRATA STORTI FOUNDATION. WoS1 |
| 2007 | Toplin, J., Fuller, C., Fletcher, L., Wong, S., Maslak, P., Cortes, J., . . . Beillard, E. (2007). An MMR control RNA for reliable monitoring of BCR-ABL transcripts in treated CML patients. In BLOOD Vol. 110 (pp. 863A-864A). Atlanta, GA: AMER SOC HEMATOLOGY. DOI |
| 2007 | Hughes, T., Saglio, G., Martinelli, G., Kim, D. -W., Soverini, S., Mueller, M., . . . Hochhaus, A. (2007). Responses and disease progression in CML-CP patients treated with nilotinib after imatinib failure appear to be affected by the BCR-ABL mutation status and types. In BLOOD Vol. 110 (pp. 101A). Atlanta, GA: AMER SOC HEMATOLOGY. DOI WoS13 |
| 2007 | Branford, S., Fletcher, L., Cross, N. C. P., Hochhaus, A., Mueller, M. C., Kim, D. -W., . . . Hughes, T. (2007). Validation of the international scale for measurement of BCR-ABL by RQ-PCR based on deriving laboratory-specific conversion factors. In BLOOD Vol. 110 (pp. 307A). Atlanta, GA: AMER SOC HEMATOLOGY. DOI WoS1 |
| 2007 | Hochhaus, A., Branford, S., Radich, J., Mueller, M. C., Shah, N., Erben, P., . . . Hughes, T. (2007). Efficacy of dasatinib in chronic phase chronic myelogenous leukemia patients after imatinib failure according to baseline BCR-ABL mutations. In JOURNAL OF CLINICAL ONCOLOGY Vol. 25 (pp. 1 page). AMER SOC CLINICAL ONCOLOGY. WoS3 |
| 2007 | Mueller, M. C., Branford, S., Radich, J., Kim, D. W., Martinelli, G., Saglio, G., . . . Hochhaus, A. (2007). Response dynamics to nilotinib depend on the type of BCR-ABL mutations in patients with chronic myelogenous leukemia (CML) after imatinib failure. In JOURNAL OF CLINICAL ONCOLOGY Vol. 25 (pp. 2 pages). AMER SOC CLINICAL ONCOLOGY. WoS4 |
| 2007 | Saglio, G., Kim, D. -W., Hochhaus, A., Soverini, S., Erben, P., Branford, S., . . . Radich, J. (2007). Correlation of clinical response to nilotinib with BCR-ABL mutation status in advanced phase chronic myelogenous leukemia (CML-AP) patients with imatinib-resistance or intolerance. In BLOOD Vol. 110 (pp. 576A-577A). Atlanta, GA: AMER SOC HEMATOLOGY. WoS4 |
| 2007 | Branford, S., Shou, Y., Lawrence, R., Rudzki, Z., & Hughes, T. (2007). The P-loop mutations Y253H and E255K/V may develop more frequently than T315I during nilotinib therapy after imatinib failure and are associated with progression in patients with Ph-positive leukemia. In HAEMATOLOGICA-THE HEMATOLOGY JOURNAL Vol. 92 (pp. 337-338). Vienna, AUSTRIA: FERRATA STORTI FOUNDATION. WoS5 |
| 2006 | Branford, S., Seymour, J. F., Grigg, A., Arthur, C., Lynch, K., & Hughes, T. (2006). Increasing frequency and marked stability of complete molecular response is observed in imatinib-treated CML patients with long-term follow up.. In BLOOD Vol. 108 (pp. 131A). Orlando, FL: AMER SOC HEMATOLOGY. WoS4 |
| 2006 | Hochhaus, A., Erben, P., Branford, S., Radich, J., Kim, D. W., Martinelli, G., . . . Baccarani, M. (2006). Hematologic and cytogenetic response dynamics to nilotinib (AMN107) depend on the type of BCR-ABL mutations in patients with chronic myelogeneous leukemia (CML) after imatinib failure.. In BLOOD Vol. 108 (pp. 225A). Orlando, FL: AMER SOC HEMATOLOGY. WoS4 |
| 2006 | Shah, N. P., Skaggs, B., Branford, S., Hughes, T. P., Nicoll, J. M., Paquette, R. L., & Sawyers, C. L. (2006). The most common dasatinib-resistant BCR-ABL kinase domain mutations in patients with chronic myeloid leukemia are sensitive to VX-680: Rationale for early combination kinase inhibitor therapy.. In BLOOD Vol. 108 (pp. 617A). Orlando, FL: AMER SOC HEMATOLOGY. DOI WoS2 |
| 2006 | Branford, S., Hughes, T., Stylian, S., Schwarer, A. P., Arthur, C., Filshie, R., . . . Taylor, K. M. (2006). Significant reduction of BCR-ABL transcripts after switching to imatinib therapy in patients with CML and complete or near-complete cytogenetic responses to interferon-alpha (IFN).. In BLOOD Vol. 108 (pp. 607A-608A). Orlando, FL: AMER SOC HEMATOLOGY. DOI WoS1 |
| 2006 | Shah, N. P., Skaggs, B., Branford, S., Hughes, T. P., Nicoll, J. M., Paquette, R. L., & Sawyers, C. L. (2006). Sequential kinase inhibitor therapy in CML patients can select for cells harboring compound BCR-ABL kinase domain mutations with increased oncogenic potency: Rationale for early combination therapy of ABL kinase inhibitors.. In BLOOD Vol. 108 (pp. 225A-226A). Orlando, FL: AMER SOC HEMATOLOGY. WoS4 |
| 2006 | Branford, S., Cross, N. C. P., Hochhaus, A., Radich, J., Saglio, G., Kim, D. W., . . . Hughes, T. (2006). First results from a collaborative initiative to develop an international scale for the measurement of BCR-ABL by RQ-PCR based on deriving laboratory-specific conversion factors.. In BLOOD Vol. 108 (pp. 221A). Orlando, FL: AMER SOC HEMATOLOGY. WoS1 |
| 2006 | Kaeda, J., Hochhaus, A., Radich, J., Branford, S., So, C., Gathmann, I., . . . Hughes, T. (2006). Patients with chronic phase CML in the IRIS study who receive imatinib mesylate (IM) 2nd line after prior IFN/Ara-C have sustained complete cytogenetic and major molecular response rates similar to 1st line IM patients.. In BLOOD Vol. 108 (pp. 607A). Orlando, FL: AMER SOC HEMATOLOGY. DOI WoS2 |
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| 2005 | Branford, S., Rudzki, Z., Lynch, K., & Hughes, T. (2005). Pre-imatinib factors can be used to define the risk of BCR-ABL mutations for patients with CML in chronic phase and identify a minority who should have regular mutation screening.. In BLOOD Vol. 106 (pp. 314A). Atlanta, GA: AMER SOC HEMATOLOGY. WoS2 |
| 2005 | Hughes, T. P., Branford, S., Reynolds, J., Koelmeyer, R., Seymour, J., Taylor, K., . . . Grigg, A. (2005). Maintenance of imatinib dose intensity in the first six months of therapy for newly diagnosed patients with CML is predictive of molecular response, independent of the ability to increase dose at a later point.. In BLOOD Vol. 106 (pp. 51A). Atlanta, GA: AMER SOC HEMATOLOGY. WoS4 |
| 2005 | Oehler, V., Branford, S., Pogosova-Agadjanyan, E., Shah, N., Sawyers, C., Mao, M., . . . Radich, J. (2005). Gene expression signatures associated with treatment and resistance to imatinib mesylate in chronic myeloid leukemia patients.. In BLOOD Vol. 106 (pp. 131A). Atlanta, GA: AMER SOC HEMATOLOGY. WoS2 |
| 2005 | Goldman, J. M., Hughes, T., Radich, J., Branford, S., Hochhaus, A., So, C., . . . Kaeda, J. (2005). Continuing reduction in level of residual disease after 4 years in patients with CML in chronic phase responding to first-line imatinib (IM) in the IRIS study.. In BLOOD Vol. 106 (pp. 51A). Atlanta, GA: AMER SOC HEMATOLOGY. WoS17 |
| 2005 | Shah, N. P., Nicoll, J. M., Branford, S., Hughes, T. P., Paquette, R. L., Talpaz, M., . . . Sawyers, C. L. (2005). Molecular analysis of dasatinib resistance mechanisms in CML patients identifies novel BCR-ABL mutations predicted to retain sensitivity to imatinib: Rationale for combination tyrosine kinase inhibitor therapy.. In BLOOD Vol. 106 (pp. 318A). Atlanta, GA: AMER SOC HEMATOLOGY. WoS11 |
| 2005 | White, D. L., Saunders, V. A., Branford, S., Lynch, K., To, L. B., & Hughes, T. P. (2005). The in-vivo level of imatinib induced kinase inhibition achieved in de-novo CML patients during the first 28 days of therapy is a powerful predictor of molecular outcome.. In BLOOD Vol. 106 (pp. 132A). Atlanta, GA: AMER SOC HEMATOLOGY. |
| 2004 | White, D. L., Saunders, V. A., Branford, S., Lyons, B., & Hughes, T. P. (2004). The combination of intrinsic sensitivity to imatinib and Sokal prognostic score is strongly predictive of molecular response in newly diagnosed CML patients treated with imatinib.. In BLOOD Vol. 104 (pp. 288A-289A). San Diego, CA: AMER SOC HEMATOLOGY. |
| 2004 | Shah, N. P., Branford, S., Hughes, T. P., Nicoll, J. M., Decillis, A. P., & Sawyers, C. L. (2004). Major cytogenetic responses to BMS-354825 in patients with chronic myeloid leukemia are associated with a one to two log reduction in <i>BCR</i>-<i>ABL</i> transcript.. In BLOOD Vol. 104 (pp. 288A). San Diego, CA: AMER SOC HEMATOLOGY. WoS4 |
| 2004 | Fossey, S. C., Ferreira-Gonzalez, A., Branford, S., Hughes, T. P., Garrett, C. T., Dumur, C. I., . . . Vnencak-Jones, C. L. (2004). Is standardization of quantitative RT-PCR assays for BCRABL transcript detection possible?. In JOURNAL OF MOLECULAR DIAGNOSTICS Vol. 6 (pp. 415). Los Angeles, CA: AMER SOC INVESTIGATIVE PATHOLOGY, INC. |
| 2004 | Hughes, T., Branford, S., Reynolds, J., Seymour, J., Taylor, K., Guzzo-Pernell, N., . . . Grigg, A. (2004). Higher-dose imatinib (600 mg/day) with selective intensification in newly diagnosed CML patients in chronic phase; Cytogenetic response rates at 12 months are superior to IRIS.. In BLOOD Vol. 104 (pp. 286A). San Diego, CA: AMER SOC HEMATOLOGY. WoS8 |
| 2004 | Paschka, P., Branford, S., Lorentz, C., Hehlmann, R., Hughes, T., & Hochhaus, A. (2004). Comparison of "log reduction from median pretherapeutic value" vs ratio BCR-ABL/ABL to express the therapeutic response in CML patients.. In BLOOD Vol. 104 (pp. 289A-290A). San Diego, CA: AMER SOC HEMATOLOGY. WoS4 |
| 2004 | Branford, S., Rudzki, Z., Grigg, A., Seymour, J., Browett, P., Taylor, K., . . . Hughes, T. (2004). The frequency of detection of BCR-ABL mutations in imatinib treated patients with chronic phase CML who attain a complete cytogenetic response (CCR) does not diminish with increasing duration of CCR but the associated loss of response is usually gradual. In BLOOD Vol. 104 (pp. 81A). San Diego, CA: AMER SOC HEMATOLOGY. WoS1 |
| 2004 | Branford, S., Rudzki, Z., Grigg, A., Seymour, J. F., Taylor, K., Browett, P., . . . Hughes, T. (2004). BCR-ABL levels continue to decrease up to 42 months after commencement of standard dose imatinib in patients with newly diagnosed chronic phase CML who achieve a major molecular response. In BLOOD Vol. 104 (pp. 82A). San Diego, CA: AMER SOC HEMATOLOGY. DOI WoS7 |
| 2003 | Radich, J., Gathmann, I., Kaeda, J., Goldman, J. M., Branford, S., Hochhaus, A., . . . Hughes, T. (2003). Molecular responses to imatinib and interferon plus ara-c in newly diagnosed CML: Efficacy of imatinib on patients after cross-over from interferon therapy and prognostic importance of molecular responses on long-term outcomes.. In BLOOD Vol. 102 (pp. 182A). SAN DIEGO, CALIFORNIA: AMER SOC HEMATOLOGY. |
| 2003 | Gabert, J., Silvy, M., Heath, A., Arlinghaus, R., Branford, S., Barbany, G., . . . Saldanha, J. (2003). Biological reference materials for <i>BCR ABL</i> RNA detection by RQ PCR assays for therapeutic monitoring and optimization.. In BLOOD Vol. 102 (pp. 373A-374A). SAN DIEGO, CALIFORNIA: AMER SOC HEMATOLOGY. WoS1 |
| 2003 | Hui, C. H., Goh, K., White, D., Branford, S., Grigg, A., Seymour, J., . . . Hughes, T. P. (2003). Mobilization of CD34+ cells from chronic myeloid leukemia patients achieving CCR on imatinib; safety and efficacy using filgrastim with or without continuation of imatinib. In BONE MARROW TRANSPLANTATION Vol. 31 (pp. S50). ISTANBUL, TURKEY: NATURE PUBLISHING GROUP. |
| 2003 | Hughes, T. P., Branford, S., Matthews, J., Seymour, J., Taylor, K., Guzzo-Pernell, N., . . . Grigg, A. (2003). Trial of higher dose imatinib with selective intensification in newly diagnosed CML patients in the chronic phase.. In BLOOD Vol. 102 (pp. 31A). SAN DIEGO, CALIFORNIA: AMER SOC HEMATOLOGY. WoS16 |
| 2003 | Branford, S., Rudzki, Z., Miller, B., Grigg, A., Seymour, J. F., Schwarer, A., . . . Hughes, T. P. (2003). Mutations in the catalytic core (P-Loop) of the BCR-ABL kinase domain of imatinib-treated chronic myeloid leukemia patients in chronic phase are strongly associated with imminent progression to blast crisis.. In BLOOD Vol. 102 (pp. 71A). SAN DIEGO, CALIFORNIA: AMER SOC HEMATOLOGY. WoS3 |
| 2003 | Branford, S., Rudzki, Z., Grigg, A., Seymour, J. F., Taylor, K., Herrmann, R., . . . Hughes, T. P. (2003). The incidence of BCR-ABL kinase mutations in chronic myeloid leukemia patients is as high in the second year of imatinib therapy as the first but survival after mutation detection is significantly longer for patients with mutations detected in the second year of therapy.. In BLOOD Vol. 102 (pp. 414A). SAN DIEGO, CALIFORNIA: AMER SOC HEMATOLOGY. WoS6 |
| 2003 | Taylor, K. M., Branford, S., Hughes, T., Schwarer, A., Arthur, C., Filshie, R., . . . Josephsen, A. (2003). Imatinib produces substantial molecular remissions in interferon-treated chronic phase (CP) chronic myeloid leukemia (CML) in longstanding complete or near complete cytogenetic remission (CCyR) - An Australasian leukemia and lymphoma group (ALLG) study.. In BLOOD Vol. 102 (pp. 907A). SAN DIEGO, CALIFORNIA: AMER SOC HEMATOLOGY. |
| 2002 | Hughes, T., Kaeda, J., Branford, S., Rudzki, Z., Hochhaus, A., Capdeville, R., . . . Radich, J. (2002). Molecular responses to imatinib (STI571) or interferon plus Ara-C as initial therapy for CML; Results in the IRIS study.. In BLOOD Vol. 100 (pp. 93A-94A). PHILADELPHIA, PENNSYLVANIA: AMER SOC HEMATOLOGY. WoS23 |
| 2002 | Branford, S., Walsh, S., Rudzki, Z., Grigg, A., Taylor, K., Durrant, S., . . . Hughes, T. (2002). Imatinib produces significantly superior molecular responses compared to interferon plus low dose ARA-C in patients with newly diagnosed chronic myeloid leukaemia in chronic phase.. In BLOOD Vol. 100 (pp. 96A). PHILADELPHIA, PENNSYLVANIA: AMER SOC HEMATOLOGY. WoS5 |
| 2002 | Branford, S., Walsh, S., Rudzki, Z., Grigg, A., Taylor, K., Herrmann, R., . . . Hughes, T. (2002). BCR-ABL kinase domain mutations in CML patients on imatinib: Incidence is correlated with duration of CML and mutations in the P-loop may be indicative of a poor outcome.. In BLOOD Vol. 100 (pp. 367A). PHILADELPHIA, PENNSYLVANIA: AMER SOC HEMATOLOGY. WoS2 |
| Year | Citation |
|---|---|
| 2019 | Yeung, D. T., Grigg, A., Shanmuganathan, N., Solterbeck, A. C., White, D. L., Branford, S., . . . Hughes, T. P. (2019). Pro-Active Dasatinib Dose Reduction Based on Trough Levels May Minimise Toxicity and Preserve Efficacy - Interim Analysis of the ALLG CML 12 Direct Study. Poster session presented at the meeting of BLOOD. FL, Orlando: ELSEVIER. DOI |
| 2019 | Yeung, D. T., Shanmuganathan, N., Grigg, A., Cunningham, I., Shortt, J., Rowling, P., . . . Hughes, T. P. (2019). Combination of Nilotinib and Pegylated Interferon Alfa-2B Results in High Rates of MR4.5 at 24 Months - Primary Analysis of the ALLG CML 11 Pinnacle Study. Poster session presented at the meeting of BLOOD. FL, Orlando: ELSEVIER. DOI WoS2 |
| 2018 | Shanmuganathan, N., Branford, S., Yong, A. S. M., Hiwase, D. K., Yeung, D. T., Ross, D. M., & Hughes, T. P. (2018). The e13a2 BCR-ABL1 Transcript Is Associated with Higher Rates of Molecular Recurrence after Treatment-Free Remission Attempts: Retrospective Analysis of the Adelaide Cohort. Poster session presented at the meeting of BLOOD. San Diego, CA: AMER SOC HEMATOLOGY. DOI WoS8 |
| 2017 | Ross, D. M., Pagani, I. S., Shanmuganathan, N., Seymour, J. F., Mills, A., Filshie, R., . . . Hughes, T. P. (2017). Long-Term Follow-up of the ALLG CML8 Twister Study of Treatment-Free Remission (TFR) in Patients with Chronic Myeloid Leukemia (CML). Poster session presented at the meeting of 59th ASH Annual Meeting & Exposition. |
| 2017 | Yeung, D., Grigg, A., Shanmuganathan, N., Cunningham, I., Shortt, J., Rowling, P., . . . Hughes, T. P. (2017). Nilotinib in Combination with Pegylated Interferon Alfa-2b for CP-CML Leads to High Molecular Response Rates: Interim Results of the Pinnacle Study. Poster session presented at the meeting of BLOOD. Atlanta, GA: AMER SOC HEMATOLOGY. |
| 2017 | Pagani, I. S., Dang, P., Kommers, I. O., Goyne, J., Saunders, V. A., Prime, J. A., . . . Ross, D. M. (2017). COMPARISON OF GENOMIC DNA AND REVERSE TRANSCRIPTASE Q-PCR FOR THE MONITORING OF FIRST-LINE IMATINIB TREATMENT: AN ALLG CML9 SUB-STUDY. Poster session presented at the meeting of HAEMATOLOGICA. Madrid, SPAIN: FERRATA STORTI FOUNDATION. |
| 2016 | Eadie, L., Saunders, V., Branford, S., Hughes, T., & White, D. (2016). Resistance mechanisms of the new allosteric inhibitor ABL001. Poster session presented at the meeting of ,. Houtson, USA. |
| 2016 | Eadie, L., Saunders, V., Leclercq, T., Branford, S., White, D. L., & Hughes, T. (2016). Abl001 Is Susceptible To Resistance Mediated By Overexpression Of Drug Transporters Abcb1 and Abcg2. Poster session presented at the meeting of .. Noosa, QLD. |
| 2016 | Cross, N., White, H., Ernst, T., Welden, L., Saglio, G., Mahon, F. X., . . . Branford, S. (2016). DEVELOPMENT AND EVALUATION OF A MR1-MR4.5 SECONDARY LYOPHILIZED CELL REFERENCE PANEL FOR BCR-ABL1 QUANTIFICATION ON THE INTERNATIONAL SCALE. Poster session presented at the meeting of HAEMATOLOGICA. Copenhagen, DENMARK: FERRATA STORTI FOUNDATION. |
| 2015 | Rivera, V. M., Branford, S., Nicolini, F. E., Pritchard, J. R., Cozgit, J. M., Kern, W., . . . Haferlach, T. (2015). A Multi-Institutional Retrospective Analysis of Tyrosine Kinase Inhibitor (TKI) Clinical and Preclinical Efficacy According to BCR-ABL Mutation Status in CP-CML Patients. Poster session presented at the meeting of BLOOD. Orlando, FL: AMER SOC HEMATOLOGY. |
| 2015 | Branford, S., Yeung, D., Altamura, H., Seymour, J. F., Ross, D. M., & Hughes, T. (2015). BCR-ABL LEVELS AT LANDMARK TIMEPOINTS BETWEEN 1-3 YEARS OF IMATINIB ARE PREDICTIVE OF TIME TO A DEEP MOLECULAR RESPONSE AND CAN GUIDE THERAPY SWITCH DECISIONS WHERE TKI DISCONTINUATION IS THE GOAL. Poster session presented at the meeting of HAEMATOLOGICA. Vienna, AUSTRIA: FERRATA STORTI FOUNDATION. |
| 2014 | Branford, S., Yeung, D., Ross, D., Parker, W., Braley, J., Seymour, J., & Hughes, T. (2014). The adverse effect of high sokal risk for first line imatinib treated patients is overcome by a rapid rate of BCR-ABL decline measured as early as 1 month of treatment. Poster session presented at the meeting of Abstract of power point presentation at 56th ASH Annual Meeting, published in Blood. San Francisco, California: American Society of Hematology. |
| 2014 | Yeung, D. T., Vidovic, L., Tang, C., White, D. L., Branford, S., Hughes, T. P., & Yong, A. S. M. (2014). KIR2DL5B Genotype Independently Predicts Poor Outcomes in CML-CP Patients Switched to Nilotinib after Suboptimal Responses to Imatinib and May Refine Prognosis in Patients with EMR Failure. Poster session presented at the meeting of BLOOD. San Francisco, CA: AMER SOC HEMATOLOGY. |
| 2014 | Parker, W. T., Phillis, S. R., Yeung, D. T., Lawrence, D., Schreiber, A., Wang, P., . . . Branford, S. (2014). Detection of BCR-ABL1 Compound and Polyclonal Mutants in Chronic Myeloid Leukemia Patients Using a Novel Next Generation Sequencing Approach That Minimises PCR and Sequencing Errors. Poster session presented at the meeting of BLOOD. San Francisco, CA: AMER SOC HEMATOLOGY. DOI WoS4 |
| 2014 | Casolari, D. A., Iarossi, D. G., Butcher, C. M., Bray, S. C., Parker, W. T., Hahn, C. N., . . . D'Andrea, R. J. (2014). Aberrant activation of epidermal growth factor receptor in MPN may respond to the kinase inhibitor gefitinib. Poster session presented at the meeting of Blood. US: American Society of Hematology. |
| 2014 | Branford, S., Yeung, D., Parker, W. T., Purins, L., Braley, J., Seymour, J. F., . . . Hughes, T. P. (2014). PROGNOSIS FOR CML PATIENTS WITH >10% BCR-ABL AFTER 3 MONTHS OF IMATINIB DEPENDS ON THE INITIAL RATE OF BCR-ABL DECLINE. Poster session presented at the meeting of HAEMATOLOGICA. Milan, ITALY: FERRATA STORTI FOUNDATION. |
| 2014 | Torra, O. S., Beppu, L., Branford, S., Fletcher, L., Ted, G., Paguirigan, A. L., . . . Radich, J. P. (2014). Paper or Plastic: RT-PCR of BCR-ABL from Blood Spots Stored and Shipped on Paper. Poster session presented at the meeting of BLOOD. AMER SOC HEMATOLOGY. |
| 2013 | Parker, W., Yeoman, A., Altamura, H., Roberts, N., Yeung, D., Jamison, B., . . . Branford, S. (2013). Additional BCR-ABL1 Mutations Identified By Sensitive Mass Spectrometry In Chronic Phase CML Patients With T315I Treated With Ponatinib Are Associated With Relatively Inferior Responses and Outcome. Poster session presented at the meeting of Blood. Amer Soc Hematology. |
| 2013 | Deininger, M., Shah, N., Cortes, J., Kim, D. W., Nicolini, F., Talpaz, M., . . . Branford, S. (2013). Impact Of Baseline (BL) Mutations, Including Low-Level and Compound Mutations, On Ponatinib Response and End Of Treatment (EOT) Mutation Analysis In Patients (Pts) With Chronic Phase Chronic Myeloid Leukemia (CP-CML). Poster session presented at the meeting of Blood. Amer Soc Hematology. WoS3 |
| 2013 | Parker, W., Phillis, S., Yeung, D., Hughes, T., Scott, H., & Branford, S. (2013). PCR-mediated recombination can lead to artificial chimera formation, which may pose as BCR-ABL1 compound mutations. Poster session presented at the meeting of Oral Sessions from the 55th ASH Annual Meeting and Exhibition, as published in Blood. New Orleans, Louisiana: American Society of Hematology. |
| 2012 | Yeung, D. T., Osborn, M. P., White, D. L., Branford, S., Kornhauser, M., Slader, C., . . . Hughes, T. P. (2012). Early Switch to Nilotinib Does Not Overcome the Adverse Outcome for CML Patients Failing to Achieve Early Molecular Response On Imatinib, Despite Excellent Overall Outcomes in the TIDEL II Trial. Poster session presented at the meeting of BLOOD. Atlanta, GA: AMER SOC HEMATOLOGY. DOI WoS8 |
| 2012 | Branford, S., Ross, D., Prime, J., Field, C., Altamura, H., Yeoman, A., . . . Hughes, T. (2012). Early Molecular Response and Female Sex Strongly Predict Achievement of Stable Undetectable <i>BCR</i>-<i>ABL1</i>, a Criterion for Imatinib Discontinuation in Patients with CML. Poster session presented at the meeting of BLOOD. GA, Atlanta: AMER SOC HEMATOLOGY. DOI WoS6 |
| 2012 | Parker, W. T., Yeoman, A. L., Jamison, B. A., Yeung, D. T., Scott, H. S., Hughes, T. P., & Branford, S. (2012). The patient's BCR-ABL1 Kinase Domain Mutation History Is Important for Decisions Regarding Tyrosine Kinase Inhibitor Therapy. Poster session presented at the meeting of BLOOD. Atlanta, GA: AMER SOC HEMATOLOGY. DOI |
| 2012 | Smith, C. C., Brown, M., Parker, W. T., Lin, K., Travers, K., Wang, S., . . . Shah, N. (2012). Single Molecule Real Time (SMRT (TM)) Sequencing Sensitively Detects the Evolution of Polyclonal and Compound BCR-ABL Mutations in Patients Who Relapse On Kinase Inhibitor Therapy. Poster session presented at the meeting of BLOOD. Atlanta, GA: AMER SOC HEMATOLOGY. |
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Defining genomic mechanisms associated with treatment response, drug resistance and early blast crisis in chronic myeloid leukaemia, NHMRC - Research Fellowship, 01/01/2017 - 31/12/2021
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Defining genomic mechanisms associated with tyrosine kinase inhibitor response, drug resistance, prognosis and progression in chronic myeloid leukaemia, Central Adelaide Local Health Network Incorporated, 21/02/2018 - 20/02/2021
| Date | Role | Research Topic | Program | Degree Type | Student Load | Student Name |
|---|---|---|---|---|---|---|
| 2025 | Co-Supervisor | Genomic Drivers and Therapeutic Vulnerabilities in Hematologic Malignancy Progression | Doctor of Philosophy | Doctorate | Full Time | Ms Yang Zhang |
| 2025 | Co-Supervisor | Genomic Drivers and Therapeutic Vulnerabilities in Hematologic Malignancy Progression | Doctor of Philosophy | Doctorate | Full Time | Ms Yang Zhang |
| 2024 | Co-Supervisor | The burden of cure: Secondary malignancy after allogeneic haematopoietic stem cell transplant | Doctor of Philosophy | Doctorate | Full Time | Miss Alia Elizabeth Cibich |
| 2024 | Co-Supervisor | Modelling resistant mutations in Chronic Myeloid Leukaemia | Doctor of Philosophy | Doctorate | Full Time | Ms Zuhal Naderi |
| 2024 | Co-Supervisor | The burden of cure: Secondary malignancy after allogeneic haematopoietic stem cell transplant | Doctor of Philosophy | Doctorate | Full Time | Miss Alia Elizabeth Cibich |
| 2024 | Co-Supervisor | Modelling resistant mutations in Chronic Myeloid Leukaemia | Doctor of Philosophy | Doctorate | Full Time | Ms Zuhal Naderi |
| 2022 | Principal Supervisor | - | Doctor of Philosophy | Doctorate | Full Time | Ms Muneeza Maqsood |
| 2021 | Principal Supervisor | Genomic Mechanisms Influencing Outcome In Chronic Myeloid Leukaemia | Doctor of Philosophy | Doctorate | Part Time | Miss Adelina Catherina B. Fernandes |
| 2021 | Principal Supervisor | Genomic Mechanisms Influencing Outcome In Chronic Myeloid Leukaemia | Doctor of Philosophy | Doctorate | Full Time | Miss Adelina Catherina B. Fernandes |
| Date | Role | Research Topic | Program | Degree Type | Student Load | Student Name |
|---|---|---|---|---|---|---|
| 2012 - 2016 | Principal Supervisor | Prognostic Markers Associated With Tyrosine Kinase Inhibitor Treatment Response and Maintenance of Treatment Free Remission in Chronic Myeloid Leukaemia | Doctor of Philosophy | Doctorate | Full Time | Prof David Yeung |
| 2006 - 2009 | Co-Supervisor | Minimal Residual Disease in Chronic Myeloid Leukaemia after Imatinib Treatment | Doctor of Philosophy | Doctorate | Full Time | Dr David Ross |