Jayesh Desai
杰耶什·德赛
MBBS, FRACP
Head, Solid Tumour Oncology; Associate Professor实体肿瘤肿瘤学主任;副教授
👥Biography 个人简介
Jayesh Desai, MBBS, FRACP is Head of Solid Tumour Oncology and Associate Professor at Peter MacCallum Cancer Centre in Melbourne, Australia's premier cancer research and treatment center. He is a leading investigator in early-phase oncology trials with particular expertise in gastrointestinal malignancies, sarcomas, and the integration of circulating tumor DNA (ctDNA) as a translational endpoint in dose escalation studies. Dr. Desai has led or co-led multiple first-in-human and phase I trials of novel targeted agents including KIT/PDGFRA inhibitors for GIST, CDK4/6 inhibitors, and immunotherapy combinations. His work on ctDNA dynamics during phase I dose escalation has been foundational in establishing ctDNA as a pharmacodynamic and early efficacy endpoint, enabling real-time assessment of drug activity in first-in-human studies without requiring serial tumor biopsies. He is a principal investigator for the Australian Phase I Consortium and has contributed to the TRIO and AGITG cooperative groups' early-phase trial portfolios. Dr. Desai has been particularly influential in the application of liquid biopsy technologies (ctDNA, circulating tumor cells) to early drug development workflows.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
ctDNA as Pharmacodynamic Endpoint in Phase I
Demonstrated that ctDNA kinetics during phase I dose escalation correlate with pharmacodynamic target modulation and early clinical benefit, establishing liquid biopsy approaches as feasible and informative translational endpoints in first-in-human trials without mandatory tissue biopsies.
KIT/PDGFRA Inhibitor Phase I in GIST
Led phase I dose escalation studies of novel KIT/PDGFRA inhibitors for imatinib-resistant GIST, including ripretinib (DCC-2618) and avapritinib (BLU-285) trials, contributing key translational data on mutation-specific drug activity and acquired resistance mechanisms.
Early Drug Development at Peter MacCallum
Built and leads the early-phase trials program at Peter MacCallum, establishing one of the leading phase I units in Asia-Pacific with integrated translational science including ctDNA monitoring, pharmacodynamic biopsies, and immune profiling.
RECIST and Novel Response Assessment in Early Trials
Contributed to the assessment of RECIST limitations for novel agents in phase I settings and investigated volumetric CT measures, metabolic PET responses, and ctDNA-based response criteria as complementary endpoints in early-phase oncology trials.
Representative Works 代表性著作
Avapritinib in KIT D816V-mutated advanced systemic mastocytosis
Nature Medicine (2021)
Phase I/II study of avapritinib demonstrating high response rates in KIT D816V-driven systemic mastocytosis, with translational data establishing KIT D816V allele burden (ctDNA) as a pharmacodynamic endpoint.
Circulating tumour DNA as a pharmacodynamic biomarker in phase I oncology trials
Clinical Cancer Research (2019)
Demonstrated feasibility and clinical utility of ctDNA monitoring as a pharmacodynamic endpoint in phase I dose escalation trials across multiple solid tumor types, correlating ctDNA kinetics with drug exposure and early clinical response.
Ripretinib (DCC-2618) Is a Switch Control KIT Inhibitor with a Novel Mechanism of Action for Imatinib-Resistant GIST
Cancer Cell (2019)
Preclinical and phase I clinical study of ripretinib demonstrating activity in KIT-mutant GIST resistant to prior TKIs, with PK/PD data establishing the basis for FDA approval.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-01-15 | All information from publicly available academic sources
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