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Mutational spectrum of TP53 gene correlates with nivolumab treatment efficacy in advanced gastric cancer (TP53MUT study).
Ando, Koji; Nakamura, Yoshiaki; Kitao, Hiroyuki; Shimokawa, Mototsugu; Kotani, Daisuke; Bando, Hideaki; Nishina, Tomohiro; Yamada, Takanobu; Yuki, Satoshi; Narita, Yukiya; Hara, Hiroki; Ohta, Takashi; Esaki, Taito; Hamamoto, Yasuo; Kato, Ken; Yamamoto, Yoshiyuki; Minashi, Keiko; Ohtsubo, Koushiro; Izawa, Naoki; Kawakami, Hisato; Kato, Takeshi; Satoh, Taroh; Okano, Naohiro; Tsuji, Akihito; Yamazaki, Kentaro; Yoshino, Takayuki; Maehara, Yoshihiko; Oki, Eiji.
Affiliation
  • Ando K; Department of Surgery and Science, Kyushu University, Fukuoka, Japan.
  • Nakamura Y; Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
  • Kitao H; Department for the Promotion of Drug and Diagnostic Development, National Cancer Center Hospital East, Kashiwa, Japan.
  • Shimokawa M; Oral Medicine Research Center, Fukuoka Dental College, Fukuoka, Japan.
  • Kotani D; Department of Biostatics, Yamaguchi University, Yamaguchi, Japan.
  • Bando H; Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
  • Nishina T; Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
  • Yamada T; Department for the Promotion of Drug and Diagnostic Development, National Cancer Center Hospital East, Kashiwa, Japan.
  • Yuki S; Department of Gastrointestinal Medical Oncology, National Hospital Organization Shikoku Cancer Center, Matsuyama, Japan.
  • Narita Y; Department of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan.
  • Hara H; Department of Gastroenterology and Hepatology, Hokkaido University Hospital, Sapporo, Japan.
  • Ohta T; Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.
  • Esaki T; Department of Gastroenterology, Saitama Cancer Center, Kitaadachi-gun, Japan.
  • Hamamoto Y; Department of Clinical Oncology, Kansai Rosai Hospital, Amagasaki, Japan.
  • Kato K; Department of Gastrointestinal and Medical Oncology, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan.
  • Yamamoto Y; Keio Cancer Center, Keio University School of Medicine, Tokyo, Japan.
  • Minashi K; Department of Head and Neck, Esophageal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Ohtsubo K; Department of Gastroenterology and Hepatology, University of Tsukuba Hospital, Tsukuba, Japan.
  • Izawa N; Division of Gastroenterology, Chiba Cancer Center, Chiba, Japan.
  • Kawakami H; Division of Medical Oncology, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
  • Kato T; Department of Clinical Oncology, St. Marianna University School of Medicine, Kawasaki, Japan.
  • Satoh T; Department of Medical Oncology, Kindai University Hospital, Osakasayama, Japan.
  • Okano N; Department of Surgery, National Hospital Organization Osaka National Hospital, Osaka, Japan.
  • Tsuji A; Center for Cancer Genomics and Precision Medicine, Osaka University Hospital, Suita, Japan.
  • Yamazaki K; Department of Medical Oncology, Kyorin University Faculty of Medicine, Mitaka, Japan.
  • Yoshino T; Department of Clinical Oncology, Kagawa University Hospital, Kita-gun, Japan.
  • Maehara Y; Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Shunto-gun, Japan.
  • Oki E; Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Br J Cancer ; 129(6): 1032-1039, 2023 10.
Article in En | MEDLINE | ID: mdl-37532830
ABSTRACT

BACKGROUND:

Although 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.

METHODS:

Sequence 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.

RESULTS:

Among 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.

CONCLUSION:

Nivolumab showed better efficacy in TP53 wt patients than in mutant patients. Among TP53 mutant patients, the frameshift type may have efficacy from nivolumab treatment.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stomach Neoplasms / Antineoplastic Agents, Immunological Type of study: Prognostic_studies Limits: Humans Language: En Journal: Br J Cancer Year: 2023 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stomach Neoplasms / Antineoplastic Agents, Immunological Type of study: Prognostic_studies Limits: Humans Language: En Journal: Br J Cancer Year: 2023 Document type: Article Affiliation country: Japan
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