Evidence map›Paper›PMID 41906780›Full record

ArticleJournal of gynecologic oncology2026

Effect of first-line poly(ADP-ribose) polymerase inhibitor on second-line platinum-based chemotherapy in epithelial ovarian cancer.

Yusuke Toyohara, Mayu Yunokawa, Ryo Nimura, Eitaro Funada, Risako Ozawa, Kei Kato, Shogo Nishino, Mayumi Kamata, Motoko Kanno, Atsushi Fusegi and 8 more

Abstract read
In one paragraph

Article in Journal of gynecologic oncology, 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

18 authors.

Yusuke ToyoharaDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0001-9417-7496
Mayu YunokawaDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan. mayu.yunokawa@jfcr.or.jp.ORCID https://orcid.org/0000-0001-7354-6977
Ryo NimuraDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0001-5040-9726
Eitaro FunadaDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0009-0005-4311-2787
Risako OzawaDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0002-4722-2845
Kei KatoDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0009-0005-3400-6069
Shogo NishinoDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0001-9493-7176
Mayumi KamataDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0003-0123-7459
Motoko KannoDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0002-7311-6704
Atsushi FusegiDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0001-6044-2781
Akiko AbeDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0002-0241-1319
Sachiho NetsuDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0003-2125-4109
Makiko OmiDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0003-1894-1864
Yoichi AokiDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0003-0481-9892
Terumi TanigawaDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0003-0164-7300
Sanshiro OkamotoDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0003-3712-1167
Hidetaka NomuraDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0002-2742-5282
Hiroyuki KanaoDepartment of Gynecology, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0003-1372-6145

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveResearch on platinum sensitivity after poly(ADP-ribose) polymerase (PARP) inhibitor administration, which offers prognostic benefits for first-line treatment of advanced epithelial ovarian cancer (EOC), is limited. Here, we evaluated the impact of first-line maintenance therapy with PARP inhibitors on the efficacy of second-line platinum-based chemotherapy in patients with advanced EOC.

methodsWe retrospectively analyzed 100 patients with platinum-sensitive recurrent EOC who received second-line platinum-based chemotherapy between 2015 and 2024. The PARP inhibitor group included 35 patients who received PARP inhibitors as first-line maintenance, whereas the control group included 65 patients who did not. Overall response rate, post-recurrence progression-free survival (PFS), and post-recurrence overall survival (OS) were compared between the groups. Subgroup analyses were conducted using homologous recombination deficiency status and platinum-free interval (PFI).

resultsThe overall response rate was significantly lower in the PARP inhibitor group (25.7%) compared with the control group (89.2%, p<0.001). Median post-recurrence PFS and OS were significantly shorter in the PARP inhibitor group compared to that in the control group. In the PARP inhibitor group, homologous recombination deficiency-positive patients did not show better outcomes than homologous recombination deficiency-negative patients. Moreover, the overall response rate for patients with 6-12 months PFI was particularly poor in the PARP inhibitor group.

conclusionFirst-line PARP inhibitor maintenance therapy may reduce the efficacy of subsequent platinum-based chemotherapy, potentially inducing platinum resistance. These findings highlight the need to reconsider treatment strategies and predictive biomarkers for second-line therapy following PARP inhibitor exposure in relapsed EOC.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, Ovarian EpithelialOvarian NeoplasmsPoly(ADP-ribose) Polymerase InhibitorsAdultAgedFemaleHumansMaintenance ChemotherapyMiddle AgedNeoplasm Recurrence, LocalProgression-Free SurvivalRetrospective StudiesPoly(ADP-ribose) Polymerase InhibitorsDrug Resistance, NeoplasmOvarian NeoplasmsPlatinum CompoundsPoly(ADP-ribose) Polymerase InhibitorsRecurrence

Identifiers

PMID41906780
PMCPMC13365731

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.