Systematic Review of Olaparib in the Treatment of Recurrent Platinum Sensitive Ovarian Cancer

ObjectiveTo systematically evaluate the efficacy and safety of olaparib in the treatment of recurrent platinum-sensitive ovarian cancer.MethodsThe Cochrane Library, PubMed, Chinese Biomedical Literature Database, CNKI, VIP Database, Wanfang Science and Technology Database were searched for randomize...

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Main Authors: Qian Chen, Xiaoli Li, Zhen Zhang, Tong Wu
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-03-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2022.858826/full
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author Qian Chen
Xiaoli Li
Zhen Zhang
Tong Wu
author_facet Qian Chen
Xiaoli Li
Zhen Zhang
Tong Wu
author_sort Qian Chen
collection DOAJ
description ObjectiveTo systematically evaluate the efficacy and safety of olaparib in the treatment of recurrent platinum-sensitive ovarian cancer.MethodsThe Cochrane Library, PubMed, Chinese Biomedical Literature Database, CNKI, VIP Database, Wanfang Science and Technology Database were searched for randomized controlled trials (RCTs) of olaparib in the treatment of recurrent platinum-sensitive ovarian cancer from the establishment of each database to January 2022. Two reviewers independently evaluated the quality of the literature, extracted the data, and cross-checked the methodological quality. Meta-analysis was performed using RevMan 5.4 software.ResultsA total of 7 RCTs were included, including 2406 patients, There were 1497 patients in treatment groups and 909 patients in the control group. Meta-analysis results showed that in terms of effectiveness, the overall survival time of patients in the olaparib group [HR=1.24, 95%CI(1.06, 1.45), P=0.006]; in terms of safety, for all grades of adverse events (including nausea, fatigue, vomiting, diarrhea, abdominal pain, and headache), [HR=1.54, 95%CI(1.38, 1.71), P=0.0002], for grade 3 or higher adverse events (including nausea, fatigue, vomiting, diarrhea, abdominal pain, and headache), [HR=2.13, 95%CI(1.61, 2.81), P=0.003], there were significant differences compared with the control group, suggesting that the risk of adverse reactions in the experimental group was higher than that in the control group. Subgroup analysis showed that only abdominal pain, headache and vomiting were not statistically significant, and other adverse reactions were statistically significant.ConclusionBased on the existing clinical evidence, olaparib in the treatment of recurrent platinum-sensitive ovarian cancer has a longer overall survival than the control group. It is an ideal regimen, but the incidence of adverse reactions is high.
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spelling doaj.art-1dcd05b416cd4d4981f1b3acf7cfc38b2022-12-22T01:40:17ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2022-03-011210.3389/fonc.2022.858826858826Systematic Review of Olaparib in the Treatment of Recurrent Platinum Sensitive Ovarian CancerQian ChenXiaoli LiZhen ZhangTong WuObjectiveTo systematically evaluate the efficacy and safety of olaparib in the treatment of recurrent platinum-sensitive ovarian cancer.MethodsThe Cochrane Library, PubMed, Chinese Biomedical Literature Database, CNKI, VIP Database, Wanfang Science and Technology Database were searched for randomized controlled trials (RCTs) of olaparib in the treatment of recurrent platinum-sensitive ovarian cancer from the establishment of each database to January 2022. Two reviewers independently evaluated the quality of the literature, extracted the data, and cross-checked the methodological quality. Meta-analysis was performed using RevMan 5.4 software.ResultsA total of 7 RCTs were included, including 2406 patients, There were 1497 patients in treatment groups and 909 patients in the control group. Meta-analysis results showed that in terms of effectiveness, the overall survival time of patients in the olaparib group [HR=1.24, 95%CI(1.06, 1.45), P=0.006]; in terms of safety, for all grades of adverse events (including nausea, fatigue, vomiting, diarrhea, abdominal pain, and headache), [HR=1.54, 95%CI(1.38, 1.71), P=0.0002], for grade 3 or higher adverse events (including nausea, fatigue, vomiting, diarrhea, abdominal pain, and headache), [HR=2.13, 95%CI(1.61, 2.81), P=0.003], there were significant differences compared with the control group, suggesting that the risk of adverse reactions in the experimental group was higher than that in the control group. Subgroup analysis showed that only abdominal pain, headache and vomiting were not statistically significant, and other adverse reactions were statistically significant.ConclusionBased on the existing clinical evidence, olaparib in the treatment of recurrent platinum-sensitive ovarian cancer has a longer overall survival than the control group. It is an ideal regimen, but the incidence of adverse reactions is high.https://www.frontiersin.org/articles/10.3389/fonc.2022.858826/fullolaparibovarian cancereffectivenesssafetytotal survival timeadverse reactions
spellingShingle Qian Chen
Xiaoli Li
Zhen Zhang
Tong Wu
Systematic Review of Olaparib in the Treatment of Recurrent Platinum Sensitive Ovarian Cancer
Frontiers in Oncology
olaparib
ovarian cancer
effectiveness
safety
total survival time
adverse reactions
title Systematic Review of Olaparib in the Treatment of Recurrent Platinum Sensitive Ovarian Cancer
title_full Systematic Review of Olaparib in the Treatment of Recurrent Platinum Sensitive Ovarian Cancer
title_fullStr Systematic Review of Olaparib in the Treatment of Recurrent Platinum Sensitive Ovarian Cancer
title_full_unstemmed Systematic Review of Olaparib in the Treatment of Recurrent Platinum Sensitive Ovarian Cancer
title_short Systematic Review of Olaparib in the Treatment of Recurrent Platinum Sensitive Ovarian Cancer
title_sort systematic review of olaparib in the treatment of recurrent platinum sensitive ovarian cancer
topic olaparib
ovarian cancer
effectiveness
safety
total survival time
adverse reactions
url https://www.frontiersin.org/articles/10.3389/fonc.2022.858826/full
work_keys_str_mv AT qianchen systematicreviewofolaparibinthetreatmentofrecurrentplatinumsensitiveovariancancer
AT xiaolili systematicreviewofolaparibinthetreatmentofrecurrentplatinumsensitiveovariancancer
AT zhenzhang systematicreviewofolaparibinthetreatmentofrecurrentplatinumsensitiveovariancancer
AT tongwu systematicreviewofolaparibinthetreatmentofrecurrentplatinumsensitiveovariancancer