Evidence map›Paper›PMID 38970121›Full record

ArticleJournal of ovarian research2024

The intratumoral microbiota biomarkers for predicting survival and efficacy of immunotherapy in patients with ovarian serous cystadenocarcinoma.

Hao Qin, Jie Liu, Yi Qu, Yang-Yang Li, Ya-Lan Xu, Yi-Fang Yan

Abstract read
In one paragraph

Article in Journal of ovarian research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

6 authors.

Hao Qin *State Key Laboratory of Molecular Oncology, National Cancer Center, National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, No.17 Panjiayuan Nanli, Chaoyang District, Beijing, 100021, China. haoqin@bjmu.edu.cn.
Jie Liu *Department of Medical Records, Air Force Medical Center, PLA, Air Force Medical University, Beijing, China.
Yi QuState Key Laboratory of Female Fertility Promotion, Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, No.49 North Huayuan Road, Haidian District, Beijing, 100191, China.
Yang-Yang LiMedical Center for Human Reproduction, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Ya-Lan XuDepartment of Obstetrics and Gynecology, Peking Union Medical College Hospital, Beijing, China.
Yi-Fang YanState Key Laboratory of Female Fertility Promotion, Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, No.49 North Huayuan Road, Haidian District, Beijing, 100191, China. yanyifangyanyf@hotmail.com.

Funding

Beijing Natural Science Foundation L232075Key Clinical Project of Peking University Third Hospital No. BYSYZD2023036National Clinical Research Center for Obstetrics and Gynecology (Peking University Third Hospital) No. BYSYSZKF2023014the Cancer Hospital of Chinese Academy of Medical Sciences-Shenzhen Hospital Cooperation Fund CFA202202023the Fundamental Research Funds for the Central Universities 3332023033the National Natural Science Foundation of China 32100647the National Natural Science Foundation of China 82304151
6 · The paper itself

Abstract

backgroundOvarian serous cystadenocarcinoma, accounting for about 90% of ovarian cancers, is frequently diagnosed at advanced stages, leading to suboptimal treatment outcomes. Given the malignant nature of the disease, effective biomarkers for accurate prediction and personalized treatment remain an urgent clinical need.

methodsIn this study, we analyzed the microbial contents of 453 ovarian serous cystadenocarcinoma and 68 adjacent non-cancerous samples. A univariate Cox regression model was used to identify microorganisms significantly associated with survival and a prognostic risk score model constructed using LASSO Cox regression analysis. Patients were subsequently categorized into high-risk and low-risk groups based on their risk scores.

resultsSurvival analysis revealed that patients in the low-risk group had a higher overall survival rate. A nomogram was constructed for easy visualization of the prognostic model. Analysis of immune cell infiltration and immune checkpoint gene expression in both groups showed that both parameters were positively correlated with the risk level, indicating an increased immune response in higher risk groups.

conclusionOur findings suggest that microbial profiles in ovarian serous cystadenocarcinoma may serve as viable clinical prognostic indicators. This study provides novel insights into the potential impact of intratumoral microbial communities on disease prognosis and opens avenues for future therapeutic interventions targeting these microorganisms.

Indexed as

Cystadenocarcinoma, SerousImmunotherapyOvarian NeoplasmsAdultAgedBiomarkers, TumorFemaleHumansMicrobiotaMiddle AgedPrognosisSurvival AnalysisBiomarkers, TumorIntratumoral microbiotaMicrobial biomarkerNomogramOvarian serous cystadenocarcinomaTCGA-OV

Identifiers

PMID38970121
PMCPMC11227176

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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.