Matthew H. Kulke
马修·库尔克
MD, MMSc
Chief, Section of Hematology and Oncology; Professor of Medicine血液肿瘤科主任,医学教授
👥Biography 个人简介
Matthew H. Kulke, MD, MMSc is Chief of Hematology and Oncology at Boston Medical Center and Professor of Medicine at Boston University School of Medicine. Previously a longtime faculty member and program director at Dana-Farber Cancer Institute and Harvard Medical School, he is one of the most influential clinical investigators in the field of neuroendocrine tumors globally, with over two decades of leadership in designing and executing pivotal phase II and phase III trials that have defined current standards of care for advanced NETs. His research encompasses pancreatic NETs, midgut carcinoids, and functional NETs with refractory carcinoid syndrome. Dr. Kulke was a principal investigator for the RADIANT series of trials evaluating everolimus in advanced NETs, including the landmark RADIANT-3 trial that led to FDA approval of everolimus for pancreatic NETs in 2011, and the RADIANT-4 trial demonstrating benefit in non-functional lung and gastrointestinal NETs. He also led the TELECAST trial that established telotristat ethyl as the first new agent for carcinoid syndrome diarrhea in decades. His translational work has characterized molecular mechanisms driving NET progression and resistance to targeted therapy. A past president of the North American Neuroendocrine Tumor Society (NANETS), Dr. Kulke has authored over 250 peer-reviewed publications and co-authored NCCN and ESMO clinical practice guidelines for NETs. He is a frequent invited speaker at ASCO, ESMO, and ENETS annual meetings.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
RADIANT Trials: Everolimus Approvals in Advanced NETs
Served as a principal investigator for the RADIANT-3 and RADIANT-4 phase III trials establishing everolimus as a standard-of-care agent for advanced pancreatic NETs and non-functional lung/GI NETs, directly leading to two FDA approvals and transforming systemic therapy options for these diseases.
TELECAST Trial: Telotristat Ethyl for Carcinoid Syndrome
Led the phase III TELECAST trial demonstrating that telotristat ethyl (an oral tryptophan hydroxylase inhibitor) significantly reduced carcinoid syndrome diarrhea frequency in patients inadequately controlled on somatostatin analogues, resulting in FDA approval of the first new oral agent for carcinoid syndrome in over 30 years.
Molecular Characterization and Biomarker Development in NETs
Conducted pioneering translational studies identifying actionable molecular alterations in pancreatic NETs (MEN1, DAXX/ATRX, mTOR pathway mutations) and correlating pathway activation with sensitivity to everolimus, providing a scientific basis for biomarker-driven patient selection in NET clinical trials.
Representative Works 代表性著作
Everolimus for Advanced Pancreatic Neuroendocrine Tumors
New England Journal of Medicine (2011)
RADIANT-3 phase III trial showing everolimus doubled progression-free survival vs placebo in advanced pancreatic NETs, establishing a new standard of care and leading to FDA approval.
Everolimus for the Treatment of Advanced, Non-Functional Neuroendocrine Tumours
The Lancet (2016)
RADIANT-4 phase III trial demonstrating that everolimus prolonged PFS in non-functional lung and gastrointestinal NETs, leading to a second FDA approval for everolimus in this broader NET population.
Telotristat Ethyl, a Tryptophan Hydroxylase Inhibitor for the Treatment of Carcinoid Syndrome
Journal of Clinical Oncology (2017)
TELECAST phase III trial establishing telotristat ethyl as effective and well-tolerated for carcinoid syndrome diarrhea refractory to somatostatin analogues.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-04-06 | All information from publicly available academic sources
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