Tumor Response Predicts Survival Time of Nivolumab Monotherapy for Advanced Gastric Cancer: A Subgroup Analysis of the DELIVER Trial (JACCRO GC-08).

gastric cancer nivolumab real-world data tumor response

Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
06 Apr 2024
Historique:
received: 01 12 2023
accepted: 05 03 2024
medline: 7 4 2024
pubmed: 7 4 2024
entrez: 6 4 2024
Statut: aheadofprint

Résumé

This prospective observational study evaluated the real-world effectiveness of nivolumab monotherapy in previously treated advanced gastric cancer (GC). A preplanned 2-year final analysis was performed to confirm survival and tumor behavior with nivolumab monotherapy. The primary endpoint was overall survival (OS). The data regarding tumor size were prospectively collected and evaluated using the RECIST criteria. Exploratory analyses were performed for survival according to the tumor response and depth of response (DpR) in patients with measurable lesions who were receiving nivolumab monotherapy as third- or later-line therapy. In 487 patients, the median OS and progression-free survival (PFS) were 5.8 (95% CI 5.3-6.9) months and 1.8 (95% CI 1.7-2.0) months, respectively. The response rate (RR) was 14.5% in 282 patients with measurable lesions. In 234 patients treated with third- or later-line, the DpR was found to be associated with PFS and OS in the Spearman analysis (r = 0.55 and 0.44, respectively) as well as using a discrete variable. When the DpR was divided into 5 groups (-20%≥DpR; -20%<DpR ≤ 0%; 0%<DpR ≤ 30%; 30%<DpR ≤ 50%; 50%<DpR) according to tumor shrinkage, clinically meaningful differences in PFS, and OS were noted. Patients with DpR of ≥30% had favorable survival time in nivolumab monotherapy as a later-line treatment. The final analysis confirmed the efficacy of nivolumab monotherapy for patients with advanced GC in routine clinical practice. The exploratory analysis indicated that increasing DpR was associated with longer median PFS and OS in nivolumab treatment at a later-line setting.

Sections du résumé

BACKGROUND BACKGROUND
This prospective observational study evaluated the real-world effectiveness of nivolumab monotherapy in previously treated advanced gastric cancer (GC). A preplanned 2-year final analysis was performed to confirm survival and tumor behavior with nivolumab monotherapy.
PATIENTS AND METHODS METHODS
The primary endpoint was overall survival (OS). The data regarding tumor size were prospectively collected and evaluated using the RECIST criteria. Exploratory analyses were performed for survival according to the tumor response and depth of response (DpR) in patients with measurable lesions who were receiving nivolumab monotherapy as third- or later-line therapy.
RESULTS RESULTS
In 487 patients, the median OS and progression-free survival (PFS) were 5.8 (95% CI 5.3-6.9) months and 1.8 (95% CI 1.7-2.0) months, respectively. The response rate (RR) was 14.5% in 282 patients with measurable lesions. In 234 patients treated with third- or later-line, the DpR was found to be associated with PFS and OS in the Spearman analysis (r = 0.55 and 0.44, respectively) as well as using a discrete variable. When the DpR was divided into 5 groups (-20%≥DpR; -20%<DpR ≤ 0%; 0%<DpR ≤ 30%; 30%<DpR ≤ 50%; 50%<DpR) according to tumor shrinkage, clinically meaningful differences in PFS, and OS were noted. Patients with DpR of ≥30% had favorable survival time in nivolumab monotherapy as a later-line treatment.
CONCLUSION CONCLUSIONS
The final analysis confirmed the efficacy of nivolumab monotherapy for patients with advanced GC in routine clinical practice. The exploratory analysis indicated that increasing DpR was associated with longer median PFS and OS in nivolumab treatment at a later-line setting.

Identifiants

pubmed: 38581687
pii: 7641801
doi: 10.1093/oncolo/oyae056
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Japan Clinical Cancer Research Organization

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press.

Auteurs

Yu Sunakawa (Y)

Department of Clinical Oncology, St. Marianna University School of Medicine, Kawasaki, Japan.

Yasuhiro Sakamoto (Y)

Department of Medical Oncology, Osaki Citizen Hospital, Osaki, Japan.

Ryohei Kawabata (R)

Department of Surgery, Sakai City Medical Center, Sakai, Japan.

Atsushi Ishiguro (A)

Department of Medical Oncology, Teine Keijinkai Hospital, Sapporo, Japan.

Yusuke Akamaru (Y)

Department of Gastrointestinal Surgery, Ikeda City Hospital, Ikeda, Japan.

Yosuke Kito (Y)

Department of Medical Oncology, Ishikawa Prefectural Central Hospital, Kanazawa, Japan.

Masazumi Takahashi (M)

Division of Gastroenterological Surgery, Yokohama Municipal Citizen's Hospital, Yokohama, Japan.

Jin Matsuyama (J)

Department of Gastroenterological Surgery, Higashi-Osaka City Medical Center, Higashi-Osaka, Japan.

Hiroshi Yabusaki (H)

Department of Gastroenterological Surgery, Niigata Cancer Center Hospital, Niigata, Japan.

Akitaka Makiyama (A)

Cancer Center, Gifu University Hospital, Gifu, Japan.

Takahisa Suzuki (T)

Department of Surgery, National Hospital Organization Kure Medical Center and Chugoku Cancer Center, Kure, Japan.

Masahiro Tsuda (M)

Department of Gastroenterolgical Oncology, Hyogo Cancer Center, Akashi, Japan.

Hisateru Yasui (H)

Deparment of Medical Oncology, Kobe City Medical Center General Hospital, Kobe, Japan.

Jun Hihara (J)

Department of Surgery, Hiroshima City North Medical Center Asa Citizens Hospital, Hiroshima, Japan.

Atsushi Takeno (A)

Department of Surgery, Kansai Rosai Hospital, Amagasaki, Japan.

Eisuke Inoue (E)

Showa University Research Administration Center, Showa University, Tokyo, Japan.

Wataru Ichikawa (W)

Division of Medical Oncology, Showa University Fujigaoka Hospital, Yokohama, Japan.

Masashi Fujii (M)

Japan Clinical Cancer Research Organization (JACCRO), Tokyo, Japan.

Classifications MeSH