| Literature DB >> 34224363 |
Hong Zheng1, Yunong Gao2, Hongyan Guo3, Li Li4, Qingshui Li5, Heng Cui6, An Lin7, Lixin Sun8, Yuanjing Hu9, Shan Kang10, Wei Duan11, Lingya Pan12, Shuzhen Wang13, Yingjie Yang14, Yunxia Li15, Weimin Kong11, Yang Xiang12, Xiaofei Tian16, Bin Ling17, Chunfang Ha15, Wenpei Bai18.
Abstract
The objective of this study was to evaluate the real-world application, efficacy, and safety data of olaparib for maintenance therapy and active treatment in patients with ovarian cancer in China. Patients with ovarian cancer from 17 institutions in China treated with olaparib as maintenance or active therapy from January 2018 to March 2020 were included in this study. The medical records were reviewed, and follow-up information was collected for analysis of the patients' clinicopathologic characteristics as well as the effectiveness and safety of olaparib. A total of 251 patients receiving olaparib were included, with 84 as maintenance therapy after first-line chemotherapy (FL-M), 97 as maintenance therapy after platinum-sensitive recurrence (PSR-M), and 70 as active treatment (AT). The probability of progression-free survival (PFS) at 12 months was 87.6% in the FL-M group and 63.8% in the PSR-M group. According to the multivariate analysis, complete response (CR) to chemotherapy for the PSR-M patients was the only factor affecting the PFS (HR = 0.414, P = 0.014), and platinum sensitivity was the only factor affecting PFS improvement in the AT group (HR = 0.317, P = 0.009). In the AT group, the objective response rate was 37.1%, the CR rate was 7.1%, and 30% of the patients had stable disease. Eight (3.2%) patients discontinued olaparib due to toxicity. Anemia was the most common adverse event. In conclusion, olaparib is effective and well tolerated in the real-world setting of ovarian cancer treatment. Platinum sensitivity is positively correlated to the effectiveness of olaparib in both maintenance and active treatment. ©2021 American Association for Cancer Research.Entities:
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Year: 2021 PMID: 34224363 DOI: 10.1158/1535-7163.MCT-20-1064
Source DB: PubMed Journal: Mol Cancer Ther ISSN: 1535-7163 Impact factor: 6.261