Evidence map›Paper›PMID 42186031›Full record

Trial reportJournal of ovarian research2026

Overall survival and long-term safety of olaparib maintenance in patients with platinum-sensitive relapsed ovarian cancer: final analyses of phase III L-MOCA trial.

Xingzhe Liu, Dan Liu, Zikun Peng, Jianqing Zhu, Weidong Zhao, Yi Huang, Ruifang An, Hong Zheng, Pengpeng Qu, Li Wang and 13 more

Abstract readClinical Trial, Phase IIIMulticenter Study
In one paragraph

Trial report in Journal of ovarian research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Xingzhe Liu *National Clinical Research Centre for Obstetrics and Gynaecology, Department of Gynecological Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Dan Liu *National Clinical Research Centre for Obstetrics and Gynaecology, Department of Gynecological Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Zikun Peng *National Clinical Research Centre for Obstetrics and Gynaecology, Department of Gynecological Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Jianqing Zhu *Department of Gynecologic Oncology, Cancer Hospital of The University of Chinese Academy of Sciences (Zhejiang Cancer Hospital), Hangzhou, China.
Weidong Zhao *Department of Gynecologic Oncology, Anhui Provincial Cancer Hospital, Hefei, China.
Yi Huang *Department of Gynecologic Oncology, Hubei Cancer Hospital, Wuhan, China.
Ruifang AnDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Hong ZhengDepartment of Gynecology, Key laboratory of Carcinogenesis and Translational Research (Ministry of Education), Beijing Cancer Hospital, Beijing, China.
Pengpeng QuDepartment of Gynecology Oncology, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin, China.
Li WangDepartment of Gynecologic Oncology, Affiliated Cancer Hospital of Zhengzhou University (Henan Cancer Hospital), Zhengzhou, China.
Qi ZhouDepartment of Gynecologic Oncology, Chongqing University Cancer Hospital, Chongqing, China.
Danbo WangDepartment of Gynecologic Oncology, Liaoning Cancer Hospital, Shenyang, China.
Ge LouDepartment of Gynecologic Oncology, Harbin Medical University Cancer Hospital, Harbin, China.
Jing WangDepartment of Gynecologic Oncology, Hunan Cancer Hospital, Changsha, China.
John LowCancer Centre @ PHKL, Pantai Hospital Kuala Lumpur, Kuala Lumpur, Malaysia.
Beihua KongDepartment of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan, China.
Rutie YinDepartment of Obstetrics and Gynecology, West China Second University Hospital, Chengdu, China.
Xing XieDepartment of Gynecologic oncology, School of Medicine, Women's Hospital, Zhejiang University, Hangzhou, China.
Jihong LiuDepartment of Gynecologic Oncology, Sun Yet Sen University Cancer Center, Guangzhou, China.
Wei SunDepartment of Gynecologic Oncology, Anhui Provincial Cancer Hospital, Hefei, China.
Rongyu ZangDepartment of Gynecologic Oncology, Zhongshan Hospital, Fudan University, 180 Fenglin Road, Xuhui District, Shanghai, 200032, China. zang.rongyu@zs-hospital.sh.cn.
Ding MaNational Clinical Research Centre for Obstetrics and Gynaecology, Department of Gynecological Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. dma@tjh.tjmu.edu.cn.
Qinglei GaoNational Clinical Research Centre for Obstetrics and Gynaecology, Department of Gynecological Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. qingleigao@hotmail.com.

Funding

National Natural Science Foundation of China #U25A20117
6 · The paper itself

Abstract

backgroundThe indications for Poly(ADP-ribose) polymerase (PARP) inhibitor maintenance therapy in platinum-sensitive recurrent ovarian cancer (PSROC) patients varies across nations. The lack of clinical trial evidence and detailed biomarker analysis in the Asian population results in uncertain clinical benefits. Additionally, the absence of long-term safety monitoring data limits the assessment of tolerance to prolonged PARP inhibitor use.

methodsThis prospective, open-label, single-arm, phase IIIb L-MOCA study enrolled Asian patients with high-grade epithelial PSROC across China and Malaysia. Patients received oral olaparib (300 mg) twice daily until disease progression or unacceptable toxicity. The primary endpoint of progression-free survival has been reported previously. A prespecified final OS analysis was conducted at approximately 60% data maturity.

resultsAfter a median follow-up of 73.4 months, the median OS (mOS) reached 51.0 months (95% CI, 42.7 to 56.1). The mOS was 64.4 months (49.9 to not reach [NR]) in BRCA-mutated patients and 40.9 months (33.3 to 51.0) in BRCA wild-type patients. The mOS was 54.4 months (42.5 to NE) in HRD-positive patients and 34.8 months (28.3 to 46.6) in HRD-negative patients. No new safety signals were identified compared to the primary L-MOCA report. Myelodysplastic syndrome and acute myeloid leukemia (MDS/AML) occurred in 1.3% of patients, and no additional cases were identified after approximately four additional years of follow-up beyond the primary analysis.

conclusionLong-term follow-up data from L-MOCA indicates that olaparib maintenance monotherapy shows promising overall survival and tolerable safety profile in Asian PSROC patients, regardless of BRCA or HRD status.

trial registrationRegistry: ClinicalTrials.gov.

Indexed as

Antineoplastic AgentsNeoplasm Recurrence, LocalOvarian NeoplasmsPhthalazinesPiperazinesPoly(ADP-ribose) Polymerase InhibitorsAdultAgedFemaleHumansMaintenance ChemotherapyMiddle AgedProspective StudiesAntineoplastic AgentsolaparibPhthalazinesPiperazinesPoly(ADP-ribose) Polymerase InhibitorsOlaparibOvarian cancerPARP inhibitorPlatinum-sensitive relapsed

Identifiers

PMID42186031
PMCPMC13386713

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.