Effect of DNA damage response mutations on prostate cancer prognosis: a systematic review.
Stephanie Louise SwiftShona Helen LangHeath WhiteKate MissoJos M P KleijnenRuben G W QuekPublished in: Future oncology (London, England) (2019)
The prognosis of men with prostate cancer (PC) with mutations in DNA damage response (DDR) genes undergoing different treatments is unclear. This systematic review compared clinical outcomes in PC patients with DDR mutations (DDR+) versus no mutations (DDR-). 14 resources plus gray literature were searched for studies in PC and subgroups (castration-resistant PC, metastatic PC and metastatic castration-resistant PC) by DDR gene (ATM, ATR, BRCA1, BRCA2, CHEK2, FANCA, MLH1, MRE11A, NBN, PALB2, RAD51C) mutation status. From 11,648 records, 26 studies were included. For mCRPC, six studies reported comparative efficacy for key outcomes. Improvements in several clinical outcomes were observed for DDR+ (vs DDR-) after PARP inhibitor therapy or immunotherapy. DDR+ PC patients may have improved outcomes depending on the treatment they undergo.
Keyphrases
- dna damage response
- prostate cancer
- dna repair
- systematic review
- squamous cell carcinoma
- dna damage
- radical prostatectomy
- ejection fraction
- end stage renal disease
- case control
- genome wide
- type diabetes
- chronic kidney disease
- mesenchymal stem cells
- randomized controlled trial
- stem cells
- metabolic syndrome
- breast cancer risk