Evidence map›Paper›PMID 38840771›Full record

ArticleMedComm2024

The combination of tumor mutational burden and T-cell receptor repertoire predicts the response to immunotherapy in patients with advanced non-small cell lung cancer.

Yalun Li, Liyan Ji, Yingqian Zhang, Jiexin Zhang, Alexandre Reuben, Hao Zeng, Qin Huang, Qi Wei, Sihan Tan, Xuefeng Xia and 3 more

Abstract read
In one paragraph

Article in MedComm, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
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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

13 authors.

Yalun LiDepartment of Pulmonary and Critical Care Medicine State Key Laboratory of Respiratory Health and Multimorbidity West China Hospital of Sichuan University, Precision Medicine Key Laboratory of Sichuan Province Chengdu Sichuan China.
Liyan JiGeneplus-Beijing Institute Beijing China.
Yingqian ZhangGeneplus-Beijing Institute Beijing China.
Jiexin ZhangDepartments of Bioinformatics and Computational Biology University of Texas MD Anderson Cancer Center Houston Texas USA.
Alexandre ReubenDepartment of Thoracic/Head and Neck Medical Oncology University of Texas MD Anderson Cancer Center Houston Texas USA.
Hao ZengDepartment of Pulmonary and Critical Care Medicine West China Hospital, West China School of Medicine, Sichuan University Chengdu Sichuan China.
Qin HuangDepartment of Pulmonary and Critical Care Medicine West China Hospital, West China School of Medicine, Sichuan University Chengdu Sichuan China.
Qi WeiDepartment of Pulmonary and Critical Care Medicine West China Hospital, West China School of Medicine, Sichuan University Chengdu Sichuan China.
Sihan TanDepartment of Pulmonary and Critical Care Medicine West China Hospital, West China School of Medicine, Sichuan University Chengdu Sichuan China.
Xuefeng XiaGeneplus-Beijing Institute Beijing China.
Weimin LiDepartment of Pulmonary and Critical Care Medicine State Key Laboratory of Respiratory Health and Multimorbidity West China Hospital of Sichuan University, Precision Medicine Key Laboratory of Sichuan Province Chengdu Sichuan China.
Jianjun ZhangDepartment of Thoracic/Head and Neck Medical Oncology University of Texas MD Anderson Cancer Center Houston Texas USA.
Panwen TianDepartment of Pulmonary and Critical Care Medicine State Key Laboratory of Respiratory Health and Multimorbidity West China Hospital of Sichuan University, Precision Medicine Key Laboratory of Sichuan Province Chengdu Sichuan China.ORCID https://orcid.org/0000-0002-6313-3228

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor mutational burden (TMB) and T-cell receptor (TCR) might predict the response to immunotherapy in patients with non-small cell lung cancer (NSCLC). However, the predictive value of the combination of TMB and TCR was not clear. Targeted DNA and TCR sequencing were performed on tumor biopsy specimens. We combined TMB and TCR diversity into a TMB-and-TCR (TMR) score using logistic regression. In total, 38 patients with advanced NSCLC were divided into a discovery set (

Indexed as

advanced non–small cell lung cancerclonalityimmunotherapyT‐cell receptorstumor mutational burden

Identifiers

PMID38840771
PMCPMC11151154

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.