Evidence map›Paper›PMID 37532830›Full record

ArticleBritish journal of cancer2023

Mutational spectrum of TP53 gene correlates with nivolumab treatment efficacy in advanced gastric cancer (TP53MUT study).

Koji Ando, Yoshiaki Nakamura, Hiroyuki Kitao, Mototsugu Shimokawa, Daisuke Kotani, Hideaki Bando, Tomohiro Nishina, Takanobu Yamada, Satoshi Yuki, Yukiya Narita and 18 more

Open access · greenAbstract read
In one paragraph

Article in British journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 10 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

28 authors at 20 institutions in 1 country.

Koji AndoDepartment of Surgery and Science, Kyushu University, Fukuoka, Japan.ORCID http://orcid.org/0000-0002-0149-1505
Yoshiaki NakamuraDepartment of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Hiroyuki KitaoOral Medicine Research Center, Fukuoka Dental College, Fukuoka, Japan.
Mototsugu ShimokawaDepartment of Biostatics, Yamaguchi University, Yamaguchi, Japan.
Daisuke KotaniDepartment of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID http://orcid.org/0000-0002-4196-555X
Hideaki BandoDepartment of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Tomohiro NishinaDepartment of Gastrointestinal Medical Oncology, National Hospital Organization Shikoku Cancer Center, Matsuyama, Japan.
Takanobu YamadaDepartment of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan.
Satoshi YukiDepartment of Gastroenterology and Hepatology, Hokkaido University Hospital, Sapporo, Japan.
Yukiya NaritaDepartment of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.
Hiroki HaraDepartment of Gastroenterology, Saitama Cancer Center, Kitaadachi-gun, Japan.ORCID http://orcid.org/0000-0003-3881-9815
Takashi OhtaDepartment of Clinical Oncology, Kansai Rosai Hospital, Amagasaki, Japan.
Taito EsakiDepartment of Gastrointestinal and Medical Oncology, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan.
Yasuo HamamotoKeio Cancer Center, Keio University School of Medicine, Tokyo, Japan.
Ken KatoDepartment of Head and Neck, Esophageal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID http://orcid.org/0000-0002-1733-5072
Yoshiyuki YamamotoDepartment of Gastroenterology and Hepatology, University of Tsukuba Hospital, Tsukuba, Japan.
Keiko MinashiDivision of Gastroenterology, Chiba Cancer Center, Chiba, Japan.
Koushiro OhtsuboDivision of Medical Oncology, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Naoki IzawaDepartment of Clinical Oncology, St. Marianna University School of Medicine, Kawasaki, Japan.
Hisato KawakamiDepartment of Medical Oncology, Kindai University Hospital, Osakasayama, Japan.ORCID http://orcid.org/0000-0002-3280-4850
Takeshi KatoDepartment of Surgery, National Hospital Organization Osaka National Hospital, Osaka, Japan.
Taroh SatohCenter for Cancer Genomics and Precision Medicine, Osaka University Hospital, Suita, Japan.
Naohiro OkanoDepartment of Medical Oncology, Kyorin University Faculty of Medicine, Mitaka, Japan.
Akihito TsujiDepartment of Clinical Oncology, Kagawa University Hospital, Kita-gun, Japan.
Kentaro YamazakiDivision of Gastrointestinal Oncology, Shizuoka Cancer Center, Shunto-gun, Japan.
Takayuki YoshinoDepartment of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.ORCID http://orcid.org/0000-0002-0489-4756
Yoshihiko MaeharaKyushu Central Hospital of the Mutual Aid Association of Public School Teachers, Fukuoka, Japan.
Eiji OkiDepartment of Surgery and Science, Kyushu University, Fukuoka, Japan. oki.eiji.857@m.kyushu-u.ac.jp.ORCID http://orcid.org/0000-0002-9763-9366
National Cancer Center Hospital East · JPKyushu University · JPAichi Cancer Center · JPChiba Cancer Center · JPFukuoka Dental College · JPHokkaido University Hospital · JPKagawa University Hospital · JPKanagawa Prefectural Hospital Organization · JPKanazawa University · JPKansai Rosai Hospital · JPKeio University · JPKindai University Hospital · JPKyorin University · JPKyushu Central Hospital of the Mutual Aid Association of Public School Teachers · JPNational Hospital Organization Kyushu Cancer Center · JPOsaka National Hospital · JPOsaka University Hospital · JPSaitama Cancer Center · JPShikoku Cancer Center · JPShizuoka Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough nivolumab has a high efficacy, reliable biomarkers are needed to predict the efficacy. We evaluated the nivolumab efficacy according to the TP53 mutation in advanced gastric cancer patients enrolled in the GI-SCREEN project.

methodsSequence data of tumour specimens and clinicopathological information of 913 patients with advanced gastric cancer who were enrolled between April 2015 and March 2017 were obtained from the GI-SCREEN database. The follow-up information of 266 patients treated with nivolumab was also provided.

resultsAmong 266 patients treated with nivolumab, the objective response rate (ORR) of TP53 wild type (wt) patients (24.6%) was higher than that of TP53 mutant patients (14.8%). Among TP53 mutant patients, the ORR of the frameshift type tended to be higher than the transition and transversion type (23.1%, 13.6%, and 13.0%, respectively). The median progression-free survival (PFS) was statistically longer in TP53 wt patients than in mutant patients (3.3 vs 2.1 months, HR 1.4, 95% CI 1.1-1.9). Among TP53 mutant patients, PFS was statistically longer in the frameshift type than in the transversion type.

conclusionNivolumab showed better efficacy in TP53 wt patients than in mutant patients. Among TP53 mutant patients, the frameshift type may have efficacy from nivolumab treatment.

Indexed as

Antineoplastic Agents, ImmunologicalStomach NeoplasmsGenes, p53HumansMutationNivolumabTreatment OutcomeTumor Suppressor Protein p53Antineoplastic Agents, ImmunologicalNivolumabTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID37532830
PMCPMC10491760
OpenAlexW4385493817

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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.