作者
Andrew T. Lenis,Vignesh Ravichandran,Samantha Brown,Syed M. Alam,Andrew Katims,Hong Truong,Peter A. Reisz,Samantha Vasselman,Barbara Nweji,Karen A. Autio,Michael J. Morris,Susan F. Slovin,Dana E. Rathkopf,Daniel C. Danila,Sungmin Woo,Hebert Alberto Vargas,Vincent P. Laudone,Behfar Ehdaie,Victor E. Reuter,Maria E. Arcila,Michael F. Berger,Agnès Viale,Howard I. Scher,Nikolaus Schultz,Anuradha Gopalan,Mark T.A. Donoghue,Irina Ostrovnaya,Konrad H. Stopsack,David B. Solit,Wassim Abida
摘要
Patients with microsatellite instability-high/mismatch repair-deficient (MSI-H/dMMR) and high tumor mutational burden (TMB-H) prostate cancers are candidates for pembrolizumab. We define the genomic features, clinical course, and response to immune checkpoint blockade (ICB) in patients with MSI-H/dMMR and TMB-H prostate cancers without MSI [TMB-H/microsatellite stable (MSS)].