Ritesh R. Kotecha,Sahil D. Doshi,Andrea Knežević,Joshua Chaim,Ying‐Bei Chen,Rachel Jacobi,Mark Zucker,Ed Reznik,Deaglan Joseph McHugh,Neil J. Shah,Emily Feld,David H. Aggen,William Rafelson,Han Xiao,Maria I. Carlo,Darren R. Feldman,Chung‐Han Lee,Robert J. Motzer,Martin H. Voss
Although different kidney cancers represent a heterogeneous group of malignancies, multiple subtypes including Von Hippel-Lindau (VHL)-altered clear cell renal cell carcinoma (ccRCC), fumarate hydratase (FH)- and succinate dehydrogenase (SDH)-deficient renal cell carcinoma (RCC), and renal medullary carcinoma (RMC) are affected by genomic instability. Synthetic lethality with poly ADP-ribose polymerase inhibitors (PARPis) has been suggested in preclinical models of these subtypes, and paired PARPis with immune checkpoint blockade (ICB) may achieve additive and/or synergistic effects in patients with previously treated advanced kidney cancers.