Evidence map›Paper›PMID 33687617›Full record

ArticleGastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association2021

Tumor mutation burden as a biomarker in resected gastric cancer via its association with immune infiltration and hypoxia.

Deqiang Wang, Ning Wang, Xiaoqin Li, Xiaofeng Chen, Bo Shen, Dongqin Zhu, Liuqing Zhu, Yaping Xu, Yangyang Yu, Yongqian Shu

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.9field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 46 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

10 authors at 3 institutions in 1 country.

Deqiang Wang *Department of Medical Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.
Ning Wang *Department of Oncology, The PLA Rocket Force Characteristic Medical Center, Beijing, China.
Xiaoqin LiDepartment of Medical Oncology, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.
Xiaofeng ChenDepartment of Medical Oncology, Jiangsu Province Hospital, Nanjing, China.
Bo ShenDepartment of Medical Oncology, The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China.
Dongqin ZhuNanjing Geneseeq Technology Inc, Nanjing, China.
Liuqing ZhuNanjing Geneseeq Technology Inc, Nanjing, China.
Yaping XuGeneplus-Beijing Institute, Beijing, China.
Yangyang YuThe Medical Department, 3D Medicines Inc, Shanghai, China.
Yongqian ShuDepartment of Medical Oncology, Jiangsu Province Hospital, Nanjing, China. shuyongqian@csco.org.cn.ORCID 0000-0003-2103-0877
Jiangsu Province Hospital · CNJiangsu University · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumor mutation burden (TMB) predicts immunotherapy efficacy in solid tumors. However, the biomarker role of TMB is still conflicting in resected tumors. We aimed to examine the association of TMB with prognosis and postoperative chemotherapy (CT) or radiochemotherapy (RCT) efficacy in resected gastric cancer (GC).

methodsWhole-exome sequencing (WES) was performed in 73 resected GC specimens. Validation cohorts included 352 patients from The Cancer Genome Atlas (TCGA) and 222 patients from the Asian Cancer Research Group (ACRG). Immune infiltration and hypoxia were evaluated by transcriptome data and immunohistochemistry assay.

resultsTMB-high GC had favorable overall survival (OS) and disease-free survival (DFS), but the OS and DFS benefits with postoperative CT/RCT were more pronounced in TMB-low GC. These findings were consistent among all three cohorts and were maintained in the pooled cohort. Stratified by stages in the pooled cohort, stage III GC benefited from postoperative CT/RCT regardless of TMB level while stage Ib/II GC benefited from postoperative CT/RCT in TMB-low but not in TMB-high subgroup. TMB positively correlated with immune infiltration which was characterized by NK cell rather than CD8 + T cell enrichment. TMB-high GC was more hypoxic than TMB-low GC, and TMB-high stage Ib/II GC was the most hypoxic.

conclusionsHigh TMB may predict favorable prognosis in resected GC but poor response to postoperative CT/RCT in stage Ib/II subgroup, which may be determined by TMB-associated immune infiltration and hypoxia, respectively.

Indexed as

AgedBiomarkers, TumorCell HypoxiaChemoradiotherapyDNA Mutational AnalysisExome SequencingFemaleGastrectomyHumansImmunohistochemistryImmunotherapyLymphocytes, Tumor-InfiltratingMaleMiddle AgedMutationNeoplasm StagingBiomarkers, TumorChemotherapyGastric cancerHypoxiaImmune infiltrationPrognosisRadiochemotherapyTumor mutation burden

Identifiers

PMID33687617
OpenAlexW3134978829

What OpenQuestion 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 OpenQuestion graph.