TY - JOUR
T1 - Comparison of poly (ADP-ribose) polymerase inhibitors (parpis) as maintenance therapy for platinum-sensitive ovarian cancer
T2 - Systematic review and network meta-analysis
AU - Stemmer, Amos
AU - Shafran, Inbal
AU - Stemmer, Salomon M.
AU - Tsoref, Daliah
N1 - Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/10
Y1 - 2020/10
N2 - Background: Three PARPis (olaparib, niraparib and rucaparib) are currently FDA-approved as maintenance therapy in newly diagnosed and recurrent ovarian cancer. However, thus far, no trial has compared the three approved PARPis in the overall population, in patients with BRCA mutations, or in those with wild-type BRCA. Methods: A frequentist network meta-analysis was used for indirect comparisons between the different PARPis with respect to progression free survival (PFS), overall survival (OS), and adverse events. Results: Overall, six randomized clinical trials involving 2,770 patients, were included in the analysis. Results from the indirect comparisons revealed no statistically significant differences between the three PARPis with respect to PFS or OS in the entire population and in patients with mutated and wild-type BRCA, separately. Niraparib showed a statistically significant increased risk for grade 3 and 4 thrombocytopenia (risk-difference [RD] from placebo: 0.3; 95% confidence interval [CI], 0.27-0.34) and any grade neutropenia (RD from placebo: 0.22; 95% CI, 0.18-0.25) as compared with the other PARPis. Conclusion: No statistically significant difference was found between the three PARPis with respect to PFS or OS (overall and in subpopulations by BRCA status). There is, however, a statistical difference in toxicity as niraparib is associated with a greater risk for thrombocytopenia and neutropenia.
AB - Background: Three PARPis (olaparib, niraparib and rucaparib) are currently FDA-approved as maintenance therapy in newly diagnosed and recurrent ovarian cancer. However, thus far, no trial has compared the three approved PARPis in the overall population, in patients with BRCA mutations, or in those with wild-type BRCA. Methods: A frequentist network meta-analysis was used for indirect comparisons between the different PARPis with respect to progression free survival (PFS), overall survival (OS), and adverse events. Results: Overall, six randomized clinical trials involving 2,770 patients, were included in the analysis. Results from the indirect comparisons revealed no statistically significant differences between the three PARPis with respect to PFS or OS in the entire population and in patients with mutated and wild-type BRCA, separately. Niraparib showed a statistically significant increased risk for grade 3 and 4 thrombocytopenia (risk-difference [RD] from placebo: 0.3; 95% confidence interval [CI], 0.27-0.34) and any grade neutropenia (RD from placebo: 0.22; 95% CI, 0.18-0.25) as compared with the other PARPis. Conclusion: No statistically significant difference was found between the three PARPis with respect to PFS or OS (overall and in subpopulations by BRCA status). There is, however, a statistical difference in toxicity as niraparib is associated with a greater risk for thrombocytopenia and neutropenia.
KW - Adverse event
KW - Network meta-analysis
KW - Ovarian cancer
KW - Overall survival
KW - Platinum-sensitive
KW - Poly (ADP-ribose) polymerase inhibitor
KW - Progression-free survival
UR - http://www.scopus.com/inward/record.url?scp=85092726706&partnerID=8YFLogxK
U2 - 10.3390/cancers12103026
DO - 10.3390/cancers12103026
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AN - SCOPUS:85092726706
SN - 2072-6694
VL - 12
SP - 1
EP - 12
JO - Cancers
JF - Cancers
IS - 10
M1 - 3026
ER -