FOLFIRINOX as second-line chemotherapy for advanced pancreatic cancer: A subset analysis of data from a nationwide multicenter observational study in Japan.


Journal

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]
ISSN: 1424-3911
Titre abrégé: Pancreatology
Pays: Switzerland
ID NLM: 100966936

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 24 04 2020
revised: 30 06 2020
accepted: 10 07 2020
pubmed: 26 9 2020
medline: 18 9 2021
entrez: 25 9 2020
Statut: ppublish

Résumé

Data on FOLFIRINOX as a second-line chemotherapy for advanced pancreatic cancer are limited. In the JASPAC06 study-a nationwide, multicenter, observational study-FOLFIRINOX for patients with unresectable or recurrent pancreatic cancer as any line of treatment showed favorable efficacy and safety in Japanese clinical practice. We performed exploratory analyses of patients with unresectable or recurrent pancreatic cancer who received FOLFIRINOX as the second-line chemotherapy in Japanese clinical settings. Of the 399 evaluable patients, 44 were eligible for inclusion in the analysis. The patients' characteristics were as follows: median age, 62 years; men, 26 (59%); Eastern Cooperative Oncology Group-Performance status 0/1, 30 (68%)/14 (32%); disease status, recurrent/local/metastatic: 4 (9%)/8 (18%)/32 (73%). The initial dose was reduced in 28 (64%) patients. The median time to treatment failure and number of cycles were 4.5 (range, 0.2-19.1) months and 6 cycles (range, 1-13 or more), respectively. The major grade 3/4 adverse events were neutropenia in 29 (66%), leucopenia in 17 (39%), anorexia in 7 (16%), febrile neutropenia in 5 (11%), and anemia in 5 (11%) patients. The median overall survival, progression-free survival, and 1-year survival rates were 10.3 (95% confidence interval [CI], 7.2-13.3), 4.1 (95% CI, 2.6-5.5) months, and 30%, respectively. Our findings suggest that FOLFIRINOX as a second-line chemotherapy for advanced pancreatic cancer was effective in patients with a good performance status. It displayed toxicity similar to that observed with its use as a first-line treatment.

Sections du résumé

BACKGROUND BACKGROUND
Data on FOLFIRINOX as a second-line chemotherapy for advanced pancreatic cancer are limited. In the JASPAC06 study-a nationwide, multicenter, observational study-FOLFIRINOX for patients with unresectable or recurrent pancreatic cancer as any line of treatment showed favorable efficacy and safety in Japanese clinical practice.
METHODS METHODS
We performed exploratory analyses of patients with unresectable or recurrent pancreatic cancer who received FOLFIRINOX as the second-line chemotherapy in Japanese clinical settings.
RESULTS RESULTS
Of the 399 evaluable patients, 44 were eligible for inclusion in the analysis. The patients' characteristics were as follows: median age, 62 years; men, 26 (59%); Eastern Cooperative Oncology Group-Performance status 0/1, 30 (68%)/14 (32%); disease status, recurrent/local/metastatic: 4 (9%)/8 (18%)/32 (73%). The initial dose was reduced in 28 (64%) patients. The median time to treatment failure and number of cycles were 4.5 (range, 0.2-19.1) months and 6 cycles (range, 1-13 or more), respectively. The major grade 3/4 adverse events were neutropenia in 29 (66%), leucopenia in 17 (39%), anorexia in 7 (16%), febrile neutropenia in 5 (11%), and anemia in 5 (11%) patients. The median overall survival, progression-free survival, and 1-year survival rates were 10.3 (95% confidence interval [CI], 7.2-13.3), 4.1 (95% CI, 2.6-5.5) months, and 30%, respectively.
CONCLUSION CONCLUSIONS
Our findings suggest that FOLFIRINOX as a second-line chemotherapy for advanced pancreatic cancer was effective in patients with a good performance status. It displayed toxicity similar to that observed with its use as a first-line treatment.

Identifiants

pubmed: 32972834
pii: S1424-3903(20)30221-0
doi: 10.1016/j.pan.2020.07.006
pii:
doi:

Substances chimiques

folfirinox 0
Oxaliplatin 04ZR38536J
Irinotecan 7673326042
UGT1A1 enzyme EC 2.4.1.-
Glucuronosyltransferase EC 2.4.1.17
Leucovorin Q573I9DVLP
Fluorouracil U3P01618RT

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1519-1525

Informations de copyright

Copyright © 2020. Published by Elsevier B.V.

Auteurs

Noritoshi Kobayashi (N)

Department of Oncology, Yokohama City University Hospital, Japan. Electronic address: norikoba@yokohama-cu.ac.jp.

Katsuhiro Omae (K)

Clinical Research Promotion Unit, Clinical Research Center, Shizuoka Cancer Center, Japan.

Yosuke Horita (Y)

Department of Chemotherapy and Internal Medicine, Toyama Prefectural Central Hospital, Japan.

Hideki Ueno (H)

Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, Japan.

Nobumasa Mizuno (N)

Department of Gastroenterology, Aichi Cancer Center, Japan.

Kazuhiro Uesugi (K)

Department of Gastroenterology, National Hospital Organization Shikoku Cancer Center, Japan.

Kentaro Sudo (K)

Division of Gastroenterology, Chiba Cancer Center, Japan.

Masato Ozaka (M)

Department of Gastroenterology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Japan.

Hideyuki Hayashi (H)

Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Japan.

Naohiro Okano (N)

Department of Medical Oncology, Kyorin University Faculty of Medicine, Japan.

Keiko Kamei (K)

Department of Surgery, Kindai University Hospital, Japan.

Atsushi Yamaguchi (A)

Department of Gastroenterology, Kure Medical Center and Chugoku Cancer Center, Japan.

Satoshi Kobayashi (S)

Department of Hepatobiliary and Pancreatic Oncology, Kanagawa Cancer Center, Japan.

Shuhei Suzuki (S)

Department of Clinical Oncology, Yamagata University Faculty of Medicine, Japan.

Shin Ishihara (S)

Department of Community Medicine, Fujita Health University, Japan.

Takashi Uchiyama (T)

Department of Surgery, Kikugawa General Hospital, Japan.

Akiko Todaka (A)

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Japan.

Akira Fukutomi (A)

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Japan.

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Classifications MeSH