The Current Status of DNA-Repair-Directed Precision Oncology Strategies in Epithelial Ovarian Cancers

被引:8
作者
Tang, Hiu [1 ]
Kulkarni, Sanat [2 ]
Peters, Christina [3 ]
Eddison, Jasper [4 ]
Al-Ani, Maryam [1 ]
Madhusudan, Srinivasan [1 ,5 ]
机构
[1] Nottingham Univ Hosp, Dept Oncol, Nottingham NG5 1PB, England
[2] Sandwell & West Birmingham Hosp, Dept Med, Lyndon B71 4HJ, England
[3] Univ Hosp Sussex NHS Fdn Trust, Sussex Canc Ctr, Dept Oncol, Brighton BN2 5BD, England
[4] Univ Birmingham, Med Sch, Coll Med & Dent Sci, Birmingham B15 2TT, England
[5] Univ Nottingham, Nottingham Biodiscovery Inst, Sch Med, Univ Pk, Nottingham NG7 3RD, England
关键词
DNA repair; ovarian cancer; synthetic lethality; precision oncology; PARPi; BRCA; NUCLEOTIDE EXCISION-REPAIR; STRAND BREAK REPAIR; GRADE SEROUS OVARIAN; HOMOLOGOUS RECOMBINATION; PHASE-III; NONPLATINUM CHEMOTHERAPY; MAINTENANCE THERAPY; MOLECULAR-MECHANISM; IONIZING-RADIATION; RANDOMIZED-TRIAL;
D O I
10.3390/ijms24087293
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Survival outcomes for patients with advanced ovarian cancer remain poor despite advances in chemotherapy and surgery. Platinum-based systemic chemotherapy can result in a response rate of up to 80%, but most patients will have recurrence and die from the disease. Recently, the DNA-repair-directed precision oncology strategy has generated hope for patients. The clinical use of poly(ADP-ribose) polymerase (PARP) inhibitors in BRCA germ-line-deficient and/or platinum-sensitive epithelial ovarian cancers has improved survival. However, the emergence of resistance is an ongoing clinical challenge. Here, we review the current clinical state of PARP inhibitors and other clinically viable targeted approaches in epithelial ovarian cancers.
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页数:22
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