Parp inhibitors as maintenance treatment in platinum sensitive recurrent ovarian cancer: An updated meta-analysis of randomized clinical trials according to BRCA mutational status

被引:62
|
作者
Tomao, Federica [1 ]
Bardhi, Erlisa [1 ]
Di Pinto, Anna [1 ]
Sassu, Carolina Maria [1 ]
Biagioli, Elena [2 ]
Petrella, Maria Cristina [3 ]
Palaia, Innocenza [1 ]
Muzii, Ludovico [1 ]
Colombo, Nicoletta [4 ]
Panici, Pierluigi Benedetti [1 ]
机构
[1] Sapienza Univ Rome, Policlin Umberto I, Dept Maternal & Child Hlth & Urol Sci, Viale Policlin 155, I-00161 Rome, Italy
[2] Ist Ric Farmacol Mario Negri IRCCS, Via Mario Negri 2, I-20156 Milan, Italy
[3] AOUC, Reparto Oncol Med, Largo G Alessandro Brambilla 3, I-50134 Florence, FI, Italy
[4] Ist Europeo Oncol, Corso PortaVittoria 49, I-20122 Milan, Italy
关键词
Maintenance therapy in ovarian cancer; Platinum sensitive ovarian cancer; Recurrent ovarian cancer; PARP inhibitors; BRCA mutation; HRD; HOMOLOGOUS RECOMBINATION; DOUBLE-BLIND; EPITHELIAL OVARIAN; FALLOPIAN-TUBE; THERAPY; CHEMOTHERAPY; DEFICIENCY; PERITONEAL; RUCAPARIB; NIRAPARIB;
D O I
10.1016/j.ctrv.2019.101909
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: This meta-analysis investigated the effectiveness of PARP inhibitors (PARPis) as maintenance treatment in platinum sensitive recurrent ovarian cancer (ROC), stratifying results based on BRCA mutational status into five different categories: whole population, germ-line BRCA mutated patients, somatic BRCA mutated patients, HRD patients and wild type population. Methods: PubMed, Medline, Scopus, EMBASE and clinicaltrials.gov, as well as meeting proceedings were searched for eligible studies that described RCTs testing the efficacy of PARPis as maintenance treatment in platinum sensitive ROC. Data were extracted independently and analysed using RevMan statistical software version 5.3. Primary end-point was progression free survival (PFS). Results: The analysis confirmed the positive effect of PARPis in patients with platinum sensitive ROC in case of germinal or somatic BRCA mutations. Specifically, HR for PFS was 0.26, 95% CI 0.21-0.31, p < 0.00001 for the mutation of BRCA gene and 0.24, 95%, CI 0.12-0.48, p < 0.0001 for the somatic alteration. In addition, in the HRD population, studies that analysed the efficacy of PARPis reported a PFS improvement with HR 0.34, 95% CI 0.26-1143, p < 0.00001. Finally, our analysis confirms the role of these drugs in prolonging PFS in the whole population with HR 0.36, 95% CI 0.32-0.42, p < 0.00001, although to a lesser extent, with a significant improvement even in wild type cancers with HR 0.49, 95%, CI 0.41-0.59, p < 0.00001). Conclusions: PARPis are effective regardless of BRCA mutational status. Future investigations are necessary to explore the use of different PARPis as monotherapy, comparing them among each other in terms of efficacy and toxicity, and exploring their potential re-use.
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页数:8
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