Jonathan R. Strosberg
乔纳森·斯特罗斯伯格
MD
Associate Member, Department of Gastrointestinal Oncology; Director, Neuroendocrine Tumor Program胃肠肿瘤学系副研究员,神经内分泌肿瘤项目主任
👥Biography 个人简介
Jonathan R. Strosberg, MD is Associate Member in Gastrointestinal Oncology and Director of the Neuroendocrine Tumor Program at Moffitt Cancer Center. He is internationally recognized as the principal investigator of the NETTER-1 trial, the landmark phase III study that established lutetium-177 DOTATATE (Lutathera) peptide receptor radionuclide therapy (PRRT) as a new standard of care for advanced midgut NETs, leading to the first FDA approval of PRRT in the United States in 2018. His research encompasses novel therapeutic strategies, biomarker discovery, and optimization of PRRT combinations in NETs. Beyond NETTER-1, Dr. Strosberg has led multiple investigator-initiated and cooperative group trials in NETs, including studies of combination PRRT plus chemotherapy and novel radioligand strategies. His translational work has characterized somatostatin receptor expression, tumor heterogeneity, and mechanisms of PRRT resistance. He has also contributed to international consensus guidelines for PRRT patient selection and dosimetry. A highly sought-after speaker at ASCO, ESMO, and the European Neuroendocrine Tumor Society (ENETS), Dr. Strosberg has authored over 200 peer-reviewed publications and is a leading advocate for nuclear medicine integration into oncology practice. He serves on the editorial boards of multiple high-impact oncology journals.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
NETTER-1 Trial: FDA Approval of Lu-177 DOTATATE PRRT
Designed and led the NETTER-1 phase III randomized trial demonstrating that lutetium-177 DOTATATE (Lutathera) dramatically prolonged progression-free survival versus high-dose octreotide LAR in patients with advanced, progressive midgut NETs, directly resulting in the first FDA and EMA approvals of PRRT for somatostatin receptor-positive NETs in 2017–2018.
Optimization of PRRT Combinations and Dosimetry
Led investigational studies evaluating PRRT in combination with chemotherapy (capecitabine/temozolomide) and exploring personalized dosimetry approaches to maximize tumor radiation dose while minimizing nephrotoxicity and hematologic toxicity, establishing principles for next-generation PRRT protocols.
Prognostic and Predictive Biomarker Research in NETs
Characterized the prognostic value of somatostatin receptor expression intensity (SSTR2), circulating biomarkers, and molecular tumor profiling in predicting response to PRRT and other NET therapies, informing patient selection criteria adopted in clinical guidelines.
Representative Works 代表性著作
Phase 3 Trial of 177Lu-Dotatate for Midgut Neuroendocrine Tumors
New England Journal of Medicine (2017)
NETTER-1 landmark phase III trial demonstrating superiority of Lu-177 DOTATATE over high-dose octreotide LAR in advanced midgut NETs, leading to regulatory approval of the first PRRT in the US.
Capecitabine and Temozolomide in Advanced Pancreatic Neuroendocrine Tumors
Journal of Clinical Oncology (2011)
Retrospective analysis establishing CAPTEM (capecitabine plus temozolomide) as a highly active regimen in pancreatic NETs, widely adopted and tested in subsequent prospective trials.
A Phase 2 Study of 177Lu-Dotatate in Combination with Capecitabine in Patients with Well-Differentiated NETs
Clinical Cancer Research (2021)
Demonstrated feasibility and promising activity of PRRT plus capecitabine combination, providing rationale for ongoing phase III evaluation of combination radioligand strategies.
🏆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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