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targeted-therapy / targeted-therapyThyroid Cancer

Steven I. Sherman

MD

🏢MD Anderson Cancer Center, University of Texas🌐USA

Professor and Deputy Division Head ad Interim, Endocrine Neoplasia & Hormonal Disorders

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Key Papers
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Awards
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Key Contributions

👥Biography 个人简介

Steven I. Sherman, MD is Professor and Deputy Division Head ad Interim of the Department of Endocrine Neoplasia and Hormonal Disorders at MD Anderson Cancer Center, where he has led thyroid oncology research for over three decades. He is one of the most prolific and influential investigators in thyroid cancer clinical pharmacology, having contributed to the development and approval of virtually every major targeted agent used in advanced thyroid cancers, including lenvatinib, sorafenib, vandetanib, cabozantinib, and the selective RET inhibitors. Dr. Sherman served as a principal investigator of SELECT, the landmark phase III trial of lenvatinib in RAI-refractory differentiated thyroid cancer published in the New England Journal of Medicine in 2015. He has also contributed to DECISION (sorafenib) and multiple early-phase trials establishing new standards of care for differentiated, medullary, and anaplastic thyroid cancers. His work on the biology of thyroid cancer progression, including loss of iodine avidity and mechanisms of dedifferentiation, has informed therapeutic redifferentiation strategies. Beyond clinical trials, Dr. Sherman has made seminal contributions to thyroid cancer staging, risk stratification, and surveillance strategies. He has served on the American Thyroid Association, NCCN, and ESMO guideline committees and is a past president of the American Thyroid Association. His publication record spans over 350 peer-reviewed papers.

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🧪Research Fields 研究领域

Differentiated Thyroid Cancer
Medullary Thyroid Cancer
Thyroid Cancer Pharmacology
Lenvatinib
Clinical Trial Design
Endocrine Neoplasia

🎓Key Contributions 主要贡献

SELECT Trial: Lenvatinib in RAI-Refractory DTC

Principal investigator of SELECT, the phase III trial demonstrating that lenvatinib achieved a 65% objective response rate and significantly prolonged PFS versus placebo in RAI-refractory DTC, leading to FDA approval and establishing lenvatinib as one of the most active agents in advanced thyroid cancer.

Thyroid Cancer Risk Stratification and Redifferentiation

Developed and validated molecular and clinical risk stratification frameworks for differentiated thyroid cancer, and contributed to early studies of trametinib, selumetinib, and other agents to restore radioiodine avidity in refractory disease.

Comprehensive Drug Development Across Thyroid Cancer Subtypes

Led or co-led clinical development programs for sorafenib, lenvatinib, vandetanib, cabozantinib, selpercatinib, and pralsetinib across differentiated, medullary, and anaplastic thyroid cancer subtypes, providing the evidence base for current standard-of-care guidelines.

Representative Works 代表性著作

[1]

Lenvatinib versus Placebo in Radioiodine-Refractory Thyroid Cancer

New England Journal of Medicine (2015)

Phase III SELECT trial demonstrating superior PFS and high response rates for lenvatinib over placebo in RAI-refractory DTC, supporting FDA approval and establishing a new standard of care.

[2]

Motesanib Diphosphate in Progressive Differentiated Thyroid Cancer

Journal of Clinical Oncology (2008)

Phase II study demonstrating clinical activity of motesanib in advanced differentiated thyroid cancer, contributing to the framework for multi-kinase inhibitor development in this disease.

[3]

Thyroid Cancer, Version 2.2022, NCCN Clinical Practice Guidelines in Oncology

Journal of the National Comprehensive Cancer Network (2022)

Comprehensive evidence-based guideline update for thyroid cancer management incorporating the latest targeted therapy approvals and molecular testing recommendations.

🏆Awards & Recognition 奖项与荣誉

🏆American Thyroid Association President (2016–2017)
🏆Endocrine Society Distinguished Educator Award
🏆MD Anderson Waun Ki Hong Award for Excellence in Clinical Research

📄Data Sources 数据来源

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

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