PMID- 37058057 OWN - NLM STAT- MEDLINE DCOM- 20230418 LR - 20231002 IS - 1536-5964 (Electronic) IS - 0025-7974 (Print) IS - 0025-7974 (Linking) VI - 102 IP - 15 DP - 2023 Apr 14 TI - Analysis of adverse events and quality of life in high-grade serous ovarian cancer patients with Olaparib maintenance therapy: A single-center study in China. PG - e33434 LID - 10.1097/MD.0000000000033434 [doi] LID - e33434 AB - Olaparib showed good efficacy and tolerability in the maintenance treatment of patients with initial therapy or high-grade serous recurrent ovarian cancer patients. This study aimed to analyze adverse events (AEs) of patients taking Olaparib and the quality of life (QoL) with Olaparib in 1 center of China. The study included 98 patients who received Olaparib and 210 patients without Olaparib from July 2018 to October 2021 for high-grade serous ovarian cancer in the Gynecology Oncology Department of Jiangsu Provincial Hospital. Information of clinicopathologic characteristics was collected from medical records. Then, we used the QLQ-C30 and Quality of Life Ovarian Cancer 28 Questionnaire (QLQ-OV28) to determine the QoL of 98 patients with and 210 patients without Olaparib. Among all 98 patients with Olaparib, 66 patients in first-line and 32 patients in more than second-line treatment. Regarding the best objective response with Olaparib maintenance in 78 patients with partial remission from most recent chemotherapy, 3 (3.84%) patients showed complete response (CR) and 6 (7.69%) showed as partial response (PR), whereas stable disease was observed in 42 patients (53.84%) and 27 patients (34.6%) showed as progression disease. AEs of Grade 3 and more were: anemia in 16 patients (16.32%), neutropenia in 20 patients (20.40%), thrombocytopenia in 4 patients (4.08%), and headache in 4 patients (4.08%). Dose reduction and drug discontinuation accounted for 73.40% and 20.40%, respectively. Olaparib as maintenance therapy increased QoL on all functioning domains and several symptom domains. Consistent with previous clinical trials, Olaparib maintenance therapy was proved safe and effective. Most patients may experience Grade 1 and 2 AEs. Olaparib maintenance therapy can increase QoL in several domains. CI - Copyright (c) 2023 the Author(s). Published by Wolters Kluwer Health, Inc. FAU - Jiang, Yi AU - Jiang Y AD - Department of Gynaecology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiangsu, China. FAU - Xu, Ting AU - Xu T AD - Department of Gynaecology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiangsu, China. FAU - Yuan, Lin AU - Yuan L AD - Department of Gynaecology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiangsu, China. FAU - Zhang, Lin AU - Zhang L AD - Department of Gynaecology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiangsu, China. FAU - Ruan, Xinjia AU - Ruan X AD - State Key Laboratory of Natural Medicines, Research Center of Biostatistics and Computational Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, China. FAU - Wu, Shan AU - Wu S AD - Department of Gynaecology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiangsu, China. FAU - Meng, Huangyang AU - Meng H AD - Department of Gynaecology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiangsu, China. FAU - Cheng, Wenjun AU - Cheng W AUID- ORCID: 0000-0002-5600-9982 AD - Department of Gynaecology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiangsu, China. LA - eng PT - Journal Article PL - United States TA - Medicine (Baltimore) JT - Medicine JID - 2985248R RN - 0 (Antineoplastic Agents) RN - WOH1JD9AR8 (olaparib) SB - IM MH - Humans MH - Female MH - *Antineoplastic Agents/adverse effects MH - Quality of Life MH - Maintenance Chemotherapy MH - *Ovarian Neoplasms/pathology MH - Neoplasm Recurrence, Local/drug therapy PMC - PMC10101289 COIS- The authors have no conflicts of interest to disclose. EDAT- 2023/04/15 06:00 MHDA- 2023/04/18 06:42 PMCR- 2023/04/14 CRDT- 2023/04/14 10:13 PHST- 2023/04/18 06:42 [medline] PHST- 2023/04/14 10:13 [entrez] PHST- 2023/04/15 06:00 [pubmed] PHST- 2023/04/14 00:00 [pmc-release] AID - 00005792-202304140-00047 [pii] AID - 10.1097/MD.0000000000033434 [doi] PST - ppublish SO - Medicine (Baltimore). 2023 Apr 14;102(15):e33434. doi: 10.1097/MD.0000000000033434.