The landscape of drug sensitivity and resistance in sarcoma.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
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История · было → стало
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Al Shihabi Ahmad, Tebon Peyton J, Nguyen Huyen Thi Lam, Chantharasamee Jomjit, Sartini Sara, Davarifar Ardalan, Jensen Alexandra Y, Diaz-Infante Miranda, Cox Hannah, Gonzalez Alfredo Enrique, Norris Summer, Sperry Jantzen, Nakashima Jonathan, Tavanaie Nasrin, Winata Helena, Fitz-Gibbon Sorel T, Yamaguchi Takafumi N, Jeong Jae H, Dry Sarah, Singh Arun S, Chmielowski Bartosz, Crompton Joseph G, Kalbasi Anusha K, Eilber Fritz C, Hornicek Francis, Bernthal Nicholas M, Nelson Scott D, Boutros Paul C, Federman Noah C, Yanagawa Jane, Soragni Alice
Аннотация
Sarcomas are rare malignancies with over 100 distinct histological subtypes. Their rarity and heterogeneity pose significant challenges to identifying effective therapies, and approved regimens show varied responses. Novel, personalized approaches to therapy are needed to improve patient outcomes. Patient-derived tumor organoids (PDTOs) model tumor behavior across an array of malignancies. We leverage PDTOs to characterize the landscape of drug resistance and sensitivity in sarcoma, collecting 194 specimens from 126 patients spanning 24 distinct sarcoma subtypes. Our high-throughput organoid screening pipeline tested single agents and combinations, with results available within a week from surgery. Drug sensitivity correlated with clinical features such as tumor subtype, treatment history, and disease trajectory. PDTO screening can facilitate optimal drug selection and mirror patient outcomes in sarcoma. We could identify at least one FDA-approved or NCCN-recommended effective regimen for 59% of the specimens, demonstrating the potential of our pipeline to provide actionable treatment information.