Evidence map›Paper›PMID 42325995›Full record

ArticleObstetrics and gynecology international2026

Earlier Comprehensive Cancer Genomic Profiling in Gynecologic Cancers May Facilitate Genotype-Matched Therapy: A Prospective Single-Institution Study.

Kazusa Nofuji, Tasuku Mariya, Tomohiro Kubo, Ayako Murota, Mizue Teramoto, Shutaro Habata, Motoki Matsuura, Masahiro Iwasaki, Aki Ishikawa, Kohichi Takada and 4 more

Abstract read
In one paragraph

Article in Obstetrics and gynecology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

14 authors.

Kazusa NofujiDepartment of Obstetrics and Gynecology, Sapporo Medical University School of Medicine, Sapporo, Japan, sapmed.ac.jp.
Tasuku MariyaDepartment of Obstetrics and Gynecology, Sapporo Medical University School of Medicine, Sapporo, Japan, sapmed.ac.jp.ORCID https://orcid.org/0000-0002-7110-980X
Tomohiro KuboDepartment of Medical Oncology, Sapporo Medical University School of Medicine, Sapporo, Japan, sapmed.ac.jp.ORCID https://orcid.org/0000-0002-5585-0972
Ayako MurotaDepartment of Gastroenterology and Hepatology, Sapporo Medical University School of Medicine, Sapporo, Japan, sapmed.ac.jp.
Mizue TeramotoDepartment of Obstetrics and Gynecology, NTT Medical Center Sapporo, Sapporo, Japan.
Shutaro HabataDepartment of Obstetrics and Gynecology, Sapporo Medical University School of Medicine, Sapporo, Japan, sapmed.ac.jp.
Motoki MatsuuraDepartment of Obstetrics and Gynecology, Sapporo Medical University School of Medicine, Sapporo, Japan, sapmed.ac.jp.ORCID https://orcid.org/0000-0002-6589-6480
Masahiro IwasakiIwasaki Women's Health Clinic, Tomakomai, Japan.
Aki IshikawaDivision of Clinical Genomics, Department of Genomic and Preventive Medicine, Sapporo Medical University School of Medicine, Sapporo, Japan, sapmed.ac.jp.
Kohichi TakadaDepartment of Medical Oncology, Sapporo Medical University School of Medicine, Sapporo, Japan, sapmed.ac.jp.ORCID https://orcid.org/0000-0002-1393-9442
Masashi IdogawaDivision of Medical Genome Sciences, Department of Genomic and Preventive Medicine, Sapporo Medical University School of Medicine, Sapporo, Japan, sapmed.ac.jp.ORCID https://orcid.org/0000-0002-8507-1726
Ichiro KinoshitaDivision of Clinical Cancer Genomics, Hokkaido University Hospital, Sapporo, Japan, hokudai.ac.jp.ORCID https://orcid.org/0000-0002-6694-8414
Akihiro SakuraiDivision of Clinical Genomics, Department of Genomic and Preventive Medicine, Sapporo Medical University School of Medicine, Sapporo, Japan, sapmed.ac.jp.
Tsuyoshi SaitoDepartment of Obstetrics and Gynecology, Sapporo Medical University School of Medicine, Sapporo, Japan, sapmed.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Personalized medicine utilizing comprehensive cancer genomic profiling (CGP) for gynecologic cancers is still in its early stages and faces numerous challenges. In this study, we aimed to elucidate the current status of CGP for gynecologic cancers at our institution. Methods: We prospectively analyzed 44 cases of gynecologic cancers that underwent CGP (FoundationOne CDx or Liquid CDx) from March 2020 to July 2022, evaluating the CGP results and clinical outcomes. Results: Forty-one cases underwent FoundationOne CDx and four underwent FoundationOne Liquid CDx testing. The distribution of cancer types consisted of 10 cases of cervical cancer, 21 cases of ovarian cancer, 7 cases of endometrial cancer, and 6 cases of sarcomas. Actionable genomic alterations were identified in 42 cases (95.5%), with 16 cases (36.4%) presenting clinically for genotype-matched therapy (GMT). However, GMT was administered in only three cases (6.8%). Among the cases without GMT, four experienced a deterioration in overall physical condition and two had complications as the reason for nonimplementation. Consideration of presumed germline pathogenic variants occurred in 10 cases (22.2%), with confirmatory testing conducted in two. In survival analysis using the Cox proportional hazards model, the presence of Conclusion: To enhance the prognosis of gynecologic cases, earlier CGP testing to expand the opportunities for GMT and the proactive introduction of

Indexed as

cancer genomic profilinggenotype-matched therapygynecologic cancer

Identifiers

PMID42325995
PMCPMC13277764

What Socratic holds

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Registered trials

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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 Socratic graph.