Evidence map›Paper›PMID 35950389›Full record

ArticleBeijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences2022

[Establishment of a mutation prediction model for evaluating the efficacy of immunotherapy in renal carcinoma].

C P Qin, Y X Song, M T Ding, F Wang, J X Lin, W B Yang, Y Q DU, Q Li, S J Liu, T Xu

Open access · greenAbstract read
In one paragraph

Article in Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 83% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 institution in 1 country.

C P QinDepartment of Urology, Peking University People' s Hospital, Beijing 100044, China.
Y X SongDepartment of Urology, Peking University People' s Hospital, Beijing 100044, China.
M T DingDepartment of Urology, Peking University People' s Hospital, Beijing 100044, China.
F WangDepartment of Urology, Peking University People' s Hospital, Beijing 100044, China.
J X LinDepartment of Urology, Peking University People' s Hospital, Beijing 100044, China.
W B YangDepartment of Urology, Peking University People' s Hospital, Beijing 100044, China.
Y Q DUDepartment of Urology, Peking University People' s Hospital, Beijing 100044, China.
Q LiDepartment of Urology, Peking University People' s Hospital, Beijing 100044, China.
S J LiuDepartment of Urology, Peking University People' s Hospital, Beijing 100044, China.
T XuDepartment of Urology, Peking University People' s Hospital, Beijing 100044, China.
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo establish a mutation prediction model for efficacy assessment, the genomic sequencing data of renal cancer patients from the MSKCC (Memorial Sloan Kettering Cancer Center) pan-cancer immunotherapy cohort was used.

methodsThe genomic sequencing data of 121 clear cell renal cell carcinoma patients treated with immune checkpoint inhibitors (ICI) in the MSKCC pan-cancer immunotherapy cohort were obtained from cBioPortal database (<a href="http://www.cbioportal.org/" target="_blank">http://www.cbioportal.org/</a>) and they were analyzed by univariate and multivariate Cox regression analysis to identify mutated genes associated with ICI treatment efficacy, and we constructed a comprehensive prediction model for drug efficacy of ICI based on mutated genes using nomogram. Survival analysis and time-dependent receiver operator characteristic curves were performed to assess the prognostic value of the model. Transcriptome and genomic sequencing data of 538 renal cell carcinoma patients were obtained from the TCGA database (<a href="https://portal.gdc.cancer.gov/" target="_blank">https://portal.gdc.cancer.gov/</a>). Gene set enrichment analysis was used to identify the potential functions of the mutated genes enrolled in the nomogram.

resultsWe used multivariate Cox regression analysis and identified mutations in

conclusion

Indexed as

Carcinoma, Renal CellKidney NeoplasmsBiomarkers, TumorHumansImmunotherapyMutationBiomarkers, TumorGene mutationImmune checkpoint inhibitorsRenal cell carcinomaResponse evaluation

Identifiers

PMID35950389
PMCPMC9385530
OpenAlexW4291020723

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.