Evidence map›Paper›PMID 37712717›Full record

ArticleCancer medicine2023

The possibility of mutations of RAS signaling genes and/or TP53 in combination as a negative prognostic impact on pathological stage I non-small cell lung cancer.

Takayuki Honda, Katsutoshi Seto, Satoshi Endo, Akira Takemoto, Kousuke Tanimoto, Masashi Kobayashi, Masatake Kitano, Rie Sakakibara, Takahiro Mitsumura, Hironori Ishibashi and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

4 citing papers in PubMed, 6 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 1 institution in 1 country.

Takayuki HondaDepartment of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Japan.ORCID 0000-0002-1628-0698
Katsutoshi SetoDepartment of Thoracic Surgery, Tokyo Medical and Dental University, Bunkyo-ku, Japan.
Satoshi EndoDepartment of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Japan.
Akira TakemotoBioresource Research Center, Tokyo Medical and Dental University, Bunkyo-ku, Japan.
Kousuke TanimotoResearch Core, Tokyo Medical and Dental University, Bunkyo-ku, Japan.ORCID 0000-0002-0826-2940
Masashi KobayashiDepartment of Thoracic Surgery, Tokyo Medical and Dental University, Bunkyo-ku, Japan.
Masatake KitanoDepartment of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Japan.
Rie SakakibaraDepartment of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Japan.
Takahiro MitsumuraDepartment of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Japan.
Hironori IshibashiDepartment of Thoracic Surgery, Tokyo Medical and Dental University, Bunkyo-ku, Japan.
Johji InazawaResearch Core, Tokyo Medical and Dental University, Bunkyo-ku, Japan.
Toshihiro TanakaBioresource Research Center, Tokyo Medical and Dental University, Bunkyo-ku, Japan.
Yasunari MiyazakiDepartment of Respiratory Medicine, Tokyo Medical and Dental University, Bunkyo-ku, Japan.ORCID 0000-0002-9073-9815
Kenichi OkuboDepartment of Thoracic Surgery, Tokyo Medical and Dental University, Bunkyo-ku, Japan.ORCID 0000-0003-1092-7814
Tokyo Medical and Dental University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe recurrence rate of non-small cell lung cancer (NSCLC) is as high as 30%, even in the cancer with pathological stage I disease. Therefore, identifying factors predictive of high-risk pathological recurrence is important. However, few studies have examined the genetic status of these tumors and its relationship to prognosis. MATERIALS AND

methodsA cohort of 328 cases of primary lung cancer that underwent complete resection at Tokyo Medical and Dental University (TMDU) was screened for 440 cancer-associated genes using panel testing. Further analyses included 92 cases of pathological stage I NSCLC who did not receive adjuvant chemotherapy. Ridge regression was performed to identify association studies mutational status and postoperative recurrence. These data were then validated using clinical and genetic data from 56 patients in The Cancer Genome Atlas (TCGA).

resultsMutations in TP53, RAS signaling genes KRAS and HRAS, and EGFR were recurrently detected. Ridge regression analysis relevant to recurrence, as well as survival analysis, performed using data from the TMDU cohort revealed significantly shorter relapse-free survival (RFS) for patients with RAS signaling or TP53 gene mutations than for those without (log-rank test, p = 0.00090). This statistical trend was also suggested in the TCGA cohort (log-rank test, p = 0.10).

conclusionMutations in RAS signaling genes and/or TP53 could be useful for the prediction of shorter RFS of patients with stage I NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungErbB ReceptorsLung NeoplasmsOncogene Protein p21(ras)HumansMutationNeoplasm Recurrence, LocalNeoplasm StagingPrognosisProto-Oncogene Proteins p21(ras)Tumor Suppressor Protein p53EGFR protein, humanErbB ReceptorsHRAS protein, humanKRAS protein, humanOncogene Protein p21(ras)Proto-Oncogene Proteins p21(ras)TP53 protein, humanTumor Suppressor Protein p53non-small cell lung cancerpathological stage IRAS signaling genesTP53

Identifiers

PMID37712717
PMCPMC10587933
OpenAlexW4386758342

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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.