Evidence map›Paper›PMID 36929579›Full record

ArticleJournal of gynecologic oncology2023

PTEN mutation predicts unfavorable fertility preserving treatment outcome in the young patients with endometrioid endometrial cancer and atypical hyperplasia.

Yu Xue, Youting Dong, Yaochen Lou, Qiaoying Lv, Weiwei Shan, Chao Wang, Xiaojun Chen

Open access · diamondAbstract read
In one paragraph

Article in Journal of gynecologic oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.4field-weighted citation impact, top 5% of its field
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

14 citing papers in PubMed, 15 citations in OpenAlex.

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  6. Double jeopardy: howFrontiers in cell and developmental biology · 2026
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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

7 authors at 2 institutions in 1 country.

Yu Xue *Department of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.ORCID 0000-0001-8319-6691
Youting Dong *Shanghai Medical college, Fudan University, Shanghai, China.ORCID 0000-0002-0464-6306
Yaochen LouDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.ORCID 0000-0002-8617-9675
Qiaoying LvDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.ORCID 0000-0003-3610-2538
Weiwei ShanDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.ORCID 0000-0001-6729-2683
Chao WangDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.ORCID 0000-0003-4636-5104
Xiaojun ChenDepartment of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China. xiaojunchen2013@sina.com.ORCID 0000-0002-5493-1500
Obstetrics and Gynecology Hospital of Fudan University · CNShanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to investigate the impact of molecular classification and PTEN, KRAS and PIK3CA gene mutation on the outcome of fertility-preserving treatment in the patients with endometrioid endometrial cancer (EEC) and endometrial atypical hyperplasia (EAH).

methodsThis is a single-center retrospective study. A total of 135 patients with EEC and EAH receiving fertility-preserving treatment and molecular classification were reviewed. The distribution of the four types of molecular classification was described. The impact of non-specific molecular profile (NSMP), mismatch repair-deficiency (MMRd), and PTEN, KRAS and PIK3CA gene mutation on the outcome of fertility-preserving treatment was analyzed.

resultsOf the patients analyzed, 86.7% (117/136) were classified as having NSMP; 14 (10.4%), MMRd; 1 (0.7%), POLEmut EAH; and 3 (2.2%), p53abn EEC. The patients having NSMP and MMRd achieved similar 16-, 32-, and 48-week complete response rates. The patients harboring tier I and tier II PTEN mutations (PTENmut-Clin) achieved lower cumulative 32-week CR rates than those with PTEN-others (without PTENmut-Clin) (22/47, 46.8% vs. 50/74, 67.6%; p=0.023; odds ratio=0.422; 95% confidence interval [CI]=0.199-0.896). Insulin-resistance (hazard ratio [HR]=0.435; 95% CI=0.269-0.702; p=0.001) and PTENmut-Clin (HR=0.535; 95% CI=0.324-0.885; p=0.015) were independent negative predictors for lower 32-week CR rates.

conclusionPTENmut-Clin is an independent risk factor for unfavorable fertility-preserving treatment outcomes in the patients with EEC and EAH. The patients with MMRd receiving fertility-preserving treatment achieved outcomes similar to those of the patients with NSMP. The molecular profiles might guide fertility-preserving treatment in the prognosis and clinical decisions.

Indexed as

Carcinoma, EndometrioidEndometrial HyperplasiaEndometrial NeoplasmsClass I Phosphatidylinositol 3-KinasesFemaleFertilityHumansHyperplasiaMutationProto-Oncogene Proteins p21(ras)PTEN PhosphohydrolaseRetrospective StudiesTreatment OutcomeClass I Phosphatidylinositol 3-KinasesProto-Oncogene Proteins p21(ras)PTEN PhosphohydrolasePTEN protein, humanEndometrial Atypical HyperplasiaEndometrial CancerFertility-Preserving TreatmentMolecular ClassificationPTEN

Identifiers

PMID36929579
PMCPMC10323299
OpenAlexW4327651130

What OpenQuestion holds

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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.