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DNA damage repair pathway alterations in metastatic clear cell renal cell carcinoma and implications on systemic therapy

Yasser Ged, Joshua Chaim, Renzo G. DiNatale, Andrea Knežević, Ritesh R. Kotecha, Maria I. Carlo, Chung‐Han Lee, Ashley A. Foster, Darren R. Feldman, Min Yuen Teo, Gopa Iyer, Timothy A. Chan, Sujata Patil, Robert J. Motzer, A. Ari Hakimi, Martin H. Voss

2020Journal for ImmunoTherapy of Cancer50 citationsDOIOpen Access PDF

Abstract

BACKGROUND: Loss-of-function alterations in DNA damage repair (DDR) genes are associated with human tumorigenesis and may determine benefit from immune-oncology (I/O) agents as shown in colon cancer. However, biologic significance and relevance to I/O in metastatic clear cell RCC (ccRCC) are unknown. METHODS: Genomic data and treatment outcomes were retrospectively collected for patients with metastatic ccRCC. Tumor and germline DNA were subject to targeted next generation sequencing across >400 genes of interest, including 34 DDR genes. Patients were dichotomized according to underlying DDR gene alteration into (1) deleterious DDR gene alterations present (Del DDR); (2) wild-type (WT) and variants of unknown significance (VUS) DDR gene alterations present (WT/VUS DDR). Association between DDR status and therapeutic benefit was investigated separately for I/O and vascular endothelial growth factor (VEGF) tyrosine kinase inhibitor (TKI) therapy. RESULTS: . Clonality analysis was performed in 27 somatic DDR mutations and 17 were clonal (63%). For patients with I/O treatment, Del DDR status was associated with superior overall survival (log-rank p=0.049); after adjusting for International Metastatic Renal Cell Carcinoma Database Consortium risks and extent of prior therapy, the HR for Del DDR was 0.41 (95% CI: 0.14-1.14; p=0.09). No association was seen with VEGF-TKI treatment (log-rank p=0.903). CONCLUSION: Del DDR alterations are recurrent genomic events in patients with advanced RCC and were mostly clonal in this cohort. Loss-of-function events in these genes may affect outcome with I/O therapy in metastatic RCC, and these hypothesis-generating results deserve further study.

Topics & Concepts

Renal cell carcinomaSystemic therapyMedicineCancer researchDNA damageOncologyBioinformaticsPathologyInternal medicineDNACancerBiologyGeneticsBreast cancerDNA Repair MechanismsRenal cell carcinoma treatmentGenetic factors in colorectal cancer
DNA damage repair pathway alterations in metastatic clear cell renal cell carcinoma and implications on systemic therapy | Litcius