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targeted-therapy / targeted-therapyGIST & Sarcoma Targeted Therapy

Suzanne George

苏珊娜·乔治

MD

🏢Dana-Farber Cancer Institute / Harvard Medical School🌐USA

Associate Professor of Medicine; Director, Sarcoma Center

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Key Papers
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Awards
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Key Contributions

👥Biography 个人简介

Suzanne George, MD is Associate Professor of Medicine at Harvard Medical School and Director of the Sarcoma Center at Dana-Farber Cancer Institute, where she leads an internationally recognized program in sarcoma and gastrointestinal stromal tumor clinical research. She is a world authority on GIST, with particular expertise in wild-type and SDH-deficient GIST—rare subtypes lacking KIT/PDGFRA mutations—and in the clinical development of second- and later-line targeted therapies for advanced GIST. Dr. George has served as a lead US investigator in pivotal trials of sunitinib, regorafenib, and ripretinib in GIST and has contributed foundational translational work on the molecular biology of succinate dehydrogenase-deficient GIST, pediatric GIST, and Carney triad. She is a past chair of the CTOS Scientific Program Committee and a co-author of NCCN guidelines for GIST. She has authored over 180 peer-reviewed publications.

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🧪Research Fields 研究领域

Gastrointestinal Stromal Tumor (GIST)
Sarcoma Targeted Therapy
Sunitinib in GIST
Regorafenib
SDH-Deficient GIST
Pediatric and Wild-Type GIST

🎓Key Contributions 主要贡献

Sunitinib as Second-Line GIST Therapy

Served as a principal US investigator in the pivotal phase III trial of sunitinib versus placebo in imatinib-resistant or intolerant advanced GIST, establishing sunitinib as the global second-line standard of care and defining genotype-specific response patterns by KIT exon mutation status.

Wild-Type and SDH-Deficient GIST Biology

Led foundational clinical and molecular studies characterizing SDH-deficient GIST and its associated syndromes (Carney triad, Carney-Stratakis syndrome, pediatric GIST), identifying hypermethylation-driven silencing of SDHC as a key mechanism and establishing this entity as a biologically and therapeutically distinct GIST subtype.

Ripretinib INVICTUS and INTRIGUE Trials

Led US participation in the INVICTUS (4th-line) and INTRIGUE (2nd-line vs sunitinib) phase III trials of ripretinib in advanced GIST, contributing to the approval and further clinical characterization of this switch-control KIT/PDGFRA inhibitor.

Translational Biomarker Research in GIST

Conducted translational studies correlating KIT/PDGFRA genotype with response to imatinib and sunitinib, and explored circulating tumor DNA as a minimally invasive biomarker for monitoring resistance evolution in advanced GIST, informing personalized treatment sequencing.

Representative Works 代表性著作

[1]

Sunitinib Malate for the Treatment of Imatinib-Refractory or Intolerant GIST

Oncologist (2011)

Comprehensive analysis of sunitinib clinical activity and genotype-response correlations in imatinib-refractory GIST, establishing KIT exon 9 mutation as a predictor of differential benefit from second-line therapy.

[2]

SDH-Deficient GIST: Characteristic Clinicopathologic, Immunohistochemical, and Molecular Features

American Journal of Surgical Pathology (2011)

Defining clinicopathological and molecular characterization of SDH-deficient GIST, establishing diagnostic criteria and distinguishing features from KIT/PDGFRA-mutant GIST.

[3]

Phase III INTRIGUE Trial: Ripretinib versus Sunitinib in Second-Line Advanced GIST

Journal of Clinical Oncology (2022)

Phase III trial comparing ripretinib and sunitinib as second-line therapy in advanced GIST, providing important data on the comparative efficacy of broad-spectrum versus sequential KIT inhibition and informing treatment sequencing strategies.

🏆Awards & Recognition 奖项与荣誉

🏆CTOS Scientific Program Committee Chair
🏆ASCO Merit Award
🏆Dana-Farber Cancer Institute Director's Award for Research Excellence

📄Data Sources 数据来源

Last updated: 2026-04-06 | All information from publicly available academic sources

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