Evidence map›Paper›PMID 29895933›Full record

Trial reportScientific reports2018

Molecular profiles and tumor mutational burden analysis in Chinese patients with gynecologic cancers.

Min Wang, Wensheng Fan, Mingxia Ye, Chen Tian, Lili Zhao, Jianfei Wang, Wenbo Han, Wen Yang, Chenglei Gu, Mingxia Li and 4 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
5.2field-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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

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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

14 authors at 4 institutions in 1 country.

Min WangDepartment of Gynecology and Obstetrics, Chinese PLA General Hospital, Beijing, P.R. China.
Wensheng FanDepartment of Gynecology and Obstetrics, Chinese PLA General Hospital, Beijing, P.R. China.
Mingxia YeDepartment of Gynecology and Obstetrics, Chinese PLA General Hospital, Beijing, P.R. China.
Chen TianBeijing Genecast Biotechnology Co., Beijing, P.R. China.
Lili ZhaoBeijing Genecast Biotechnology Co., Beijing, P.R. China.
Jianfei WangBeijing Genecast Biotechnology Co., Beijing, P.R. China.
Wenbo HanBeijing Genecast Biotechnology Co., Beijing, P.R. China.
Wen YangDepartment of Gynecology and Obstetrics, Chinese PLA General Hospital, Beijing, P.R. China.
Chenglei GuDepartment of Gynecology and Obstetrics, Chinese PLA General Hospital, Beijing, P.R. China.
Mingxia LiDepartment of Gynecology and Obstetrics, Chinese PLA General Hospital, Beijing, P.R. China.
Zhe ZhangDepartment of Gynecology and Obstetrics, Chinese PLA General Hospital, Beijing, P.R. China.
Yongjun WangDepartment of Gynecology and Obstetrics, Peking University International Hospital, Beijing, P.R. China.
Henghui ZhangInstitute of Infectious Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing, P.R. China. zhhbao@ccmu.edu.cn.
Yuanguang MengDepartment of Gynecology and Obstetrics, Chinese PLA General Hospital, Beijing, P.R. China. meng6512@vip.sina.com.
Chinese PLA General Hospital · CNGenecast (China) · CNPeking University International Hospital · CNThe 309th Hospital of Chinese People's Liberation Army · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The goal of this work was to investigate the tumor mutational burden (TMB) in Chinese patients with gynecologic cancer. In total, 117 patients with gynecologic cancers were included in this study. Both tumor DNA and paired blood cell genomic DNA were isolated from formalin-fixed paraffin-embedded (FFPE) specimens and blood samples, and next-generation sequencing was performed to identify somatic mutations. TP53, PTEN, ARID1A, and PIK3CA alterations were significantly different in various types of gynecologic cancers (p = 0.001, 1.15E-07, 0.004, and 0.009, respectively). The median TMB of all 117 gynecologic tumor specimens was 0.37 mutations/Mb, with a range of 0-41.45 mutations/Mb. Despite the lack of significant difference, endometrial cancer cases had a higher median TMB than cervical and ovarian cancer cases. Younger gynecologic cancer patients (age <40 years) had a significantly lower TMB than older patients (age ≥40 years) (p = 0.04). In addition, TMB was significantly increased with increasing clinical stage of disease (p = 0.001). PTEN alterations were commonly observed in patients with a moderate to high TMB (n = 8, 38.10%, p = 9.95E-04). Although limited by sample size, all of the patients with TSC2 (n = 3, p = 3.83E-11) or POLE (n = 2, p = 0.005) mutations had a moderate to high TMB. Further large-scale, prospective studies are needed to validate our findings.

Indexed as

High-Throughput Nucleotide SequencingMutationAdolescentAdultAgedAged, 80 and overAsian PeopleChinaDNA Mutational AnalysisFemaleGenital Neoplasms, FemaleHumansMiddle AgedNeoplasm ProteinsNeoplasm Proteins

Identifiers

PMID29895933
PMCPMC5997642
OpenAlexW2806762722

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 OpenQuestion graph.