Somatic ERCC2 Mutations Correlate with Cisplatin Sensitivity in Muscle-Invasive Urothelial Carcinoma
Broad Institute · Dana-Farber Cancer Institute · +6 more institutions
Abstract
UNLABELLED: Cisplatin-based chemotherapy is the standard of care for patients with muscle-invasive urothelial carcinoma. Pathologic downstaging to pT0/pTis after neoadjuvant cisplatin-based chemotherapy is associated with improved survival, although molecular determinants of cisplatin response are incompletely understood. We performed whole-exome sequencing on pretreatment tumor and germline DNA from 50 patients with muscle-invasive urothelial carcinoma who received neoadjuvant cisplatin-based chemotherapy followed by cystectomy (25 pT0/pTis "responders," 25 pT2+ "nonresponders") to identify somatic mutations that occurred preferentially in responders. ERCC2, a nucleotide excision repair gene, was the only…
Citation impact
- FWCI
- 40.15
- Percentile
- 100%
- References
- 44
Authors
34- EMEliezer M. Van Allen
Broad Institute, Dana-Farber Cancer Institute
- KWKent W. Mouw
Dana-Farber Cancer Institute, Ziopharm Oncology (United States)
- PKPhilip Kim
Memorial Sloan Kettering Cancer Center
- GIGopa Iyer
Memorial Sloan Kettering Cancer Center, Cornell University
- NWNikhil Wagle
Broad Institute, Dana-Farber Cancer Institute
Topics & keywords
- ERCC2
- Cisplatin
- Cancer research
- Germline mutation
- Bladder cancer
- Chemotherapy
- DNA repair
- Medicine
- Good health and well-being