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Translational Medicine / 转化医学Lung Cancer & Thoracic Oncology

Alexander Drilon

MD

🏢Memorial Sloan Kettering Cancer Center🌐USA

Chief of Early Drug Development Service; Attending Physician

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Key Papers
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Awards
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Key Contributions

👥Biography 个人简介

Alexander Drilon, MD, is the Chief of Early Drug Development Service and an Attending Physician at Memorial Sloan Kettering Cancer Center, and one of the world's leading authorities on RET- and NTRK-rearranged cancers. His research has been central to the clinical development of selective RET inhibitors—selpercatinib (LOXO-292) and pralsetinib—which achieved landmark response rates in RET fusion-positive non-small cell lung cancer and thyroid cancer, transforming a historically challenging molecular subtype into one with highly effective targeted therapy options. He has also been a key investigator in the development of larotrectinib and entrectinib, the first tumor-agnostic NTRK inhibitors approved by the FDA. Drilon's expertise in oncogene-driven cancers extends across multiple molecular subtypes including MET exon 14 skipping mutations, NRG1 fusions, HER2 mutations, and FGFR alterations, reflecting his role as a leading early drug development investigator at MSK. He has conducted and led numerous first-in-human and phase II trials for novel targeted agents, establishing response rates, characterizing resistance mechanisms, and identifying companion biomarker strategies. His translational work on RET resistance has defined secondary RET mutations and bypass pathway activation as key mechanisms, informing the design of combination and next-generation strategies. Drilon is a prolific author and frequent international speaker who has contributed to ASCO, NCCN, and IASLC guidelines on the management of molecularly defined NSCLC subtypes. He is an active mentor committed to training the next generation of thoracic oncology investigators and early-phase clinical trialists. His career represents the transformative power of molecular precision oncology applied systematically across multiple rare but targetable genomic alterations.

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🧪Research Fields 研究领域

RET fusions in lung cancer
NTRK fusions
Selpercatinib
Pralsetinib
Tumor-agnostic targeted therapy

🎓Key Contributions 主要贡献

Selpercatinib in RET Fusion-Positive NSCLC

Led the LIBRETTO-001 phase I/II trial demonstrating high response rates and durable activity of selpercatinib in RET fusion-positive NSCLC including in the CNS, leading to FDA approval and establishing a new standard for RET-driven disease.

NTRK Inhibitor Development

Contributed to pivotal trials of larotrectinib and entrectinib demonstrating high tumor-agnostic response rates in NTRK fusion-positive cancers regardless of tumor histology, supporting the first tumor-agnostic FDA drug approvals.

RET Resistance Mechanisms

Characterized mechanisms of acquired resistance to first-generation RET inhibitors and evaluated next-generation strategies including novel RET inhibitor combinations and agents targeting specific resistance mutations.

Rare Oncogenic Driver Targets in NSCLC

Defined the clinical significance and therapeutic vulnerabilities of emerging molecular drivers including MET exon 14 skipping, NRG1 fusions, HER2 mutations, and FGFR alterations, expanding the landscape of actionable targets in NSCLC.

Representative Works 代表性著作

[1]

Selpercatinib in RET Fusion-Positive Non-Small-Cell Lung Cancer (LIBRETTO-001)

New England Journal of Medicine (2020)

Phase I/II trial reporting high overall response rates and durable benefit with selpercatinib in RET fusion-positive NSCLC and thyroid cancer, supporting FDA approval as the first selective RET inhibitor.

[2]

Efficacy of Larotrectinib in TRK Fusion-Positive Cancers in Adults and Children

New England Journal of Medicine (2018)

Pivotal tumor-agnostic trial demonstrating high and durable response rates with larotrectinib across 17 tumor types harboring NTRK fusions, leading to the first histology-independent FDA drug approval.

[3]

Antitumor Activity of Crizotinib in Lung Cancers Harboring a MET Exon 14 Skipping Mutation

New England Journal of Medicine (2020)

Demonstrated clinically meaningful activity of crizotinib in MET exon 14 skipping-mutant NSCLC, establishing MET as an actionable driver and supporting FDA accelerated approval of MET inhibitors in this subtype.

🏆Awards & Recognition 奖项与荣誉

🏆ASCO Young Investigator Award
🏆IASLC Thomas J. Lynch Award for Outstanding Clinical Research
🏆MSK Excellence in Clinical Research Award

📄Data Sources 数据来源

Last updated: 2026-04-05 | All information from publicly available academic sources

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