Combination gemcitabine plus S-1 versus gemcitabine plus cisplatin for advanced/recurrent biliary tract cancer: the FUGA-BT (JCOG1113) randomized phase III clinical trial.


Journal

Annals of oncology : official journal of the European Society for Medical Oncology
ISSN: 1569-8041
Titre abrégé: Ann Oncol
Pays: England
ID NLM: 9007735

Informations de publication

Date de publication:
01 12 2019
Historique:
pubmed: 1 10 2019
medline: 28 7 2020
entrez: 1 10 2019
Statut: ppublish

Résumé

Gemcitabine plus cisplatin (GC) is the standard treatment of advanced biliary tract cancer (BTC); however, it causes nausea, vomiting, and anorexia, and requires hydration. Gemcitabine plus S-1 (GS) reportedly has equal to, or better, efficacy and an acceptable toxicity profile. We aimed to confirm the non-inferiority of GS to GC for patients with advanced/recurrent BTC in terms of overall survival (OS). We undertook a phase III randomized trial in 33 institutions in Japan. Eligibility criteria included chemotherapy-naïve patients with recurrent or unresectable BTC, an Eastern Cooperative Oncology Group Performance Status of 0 - 1, and adequate organ function. The calculated sample size was 350 with a one-sided α of 5%, a power of 80%, and non-inferiority margin hazard ratio (HR) of 1.155. The primary end point was OS, while the secondary end points included progression-free survival (PFS), response rate (RR), adverse events (AEs), and clinically significant AEs defined as grade ≥2 fatigue, anorexia, nausea, vomiting, oral mucositis, or diarrhea. Between May 2013 and March 2016, 354 patients were enrolled. GS was found to be non-inferior to GC [median OS: 13.4 months with GC and 15.1 months with GS, HR, 0.945; 90% confidence interval (CI), 0.78-1.15; P = 0.046 for non-inferiority]. The median PFS was 5.8 months with GC and 6.8 months with GS (HR 0.86; 95% CI 0.70-1.07). The RR was 32.4% with GC and 29.8% with GS. Both treatments were generally well-tolerated. Clinically significant AEs were observed in 35.1% of patients in the GC arm and 29.9% in the GS arm. GS, which does not require hydration, should be considered a new, convenient standard of care option for patients with advanced/recurrent BTC. This trial has been registered with the UMIN Clinical Trials Registry (http://www.umin.ac.jp/ctr/index.htm), number UMIN000010667.

Sections du résumé

BACKGROUND
Gemcitabine plus cisplatin (GC) is the standard treatment of advanced biliary tract cancer (BTC); however, it causes nausea, vomiting, and anorexia, and requires hydration. Gemcitabine plus S-1 (GS) reportedly has equal to, or better, efficacy and an acceptable toxicity profile. We aimed to confirm the non-inferiority of GS to GC for patients with advanced/recurrent BTC in terms of overall survival (OS).
PATIENTS AND METHODS
We undertook a phase III randomized trial in 33 institutions in Japan. Eligibility criteria included chemotherapy-naïve patients with recurrent or unresectable BTC, an Eastern Cooperative Oncology Group Performance Status of 0 - 1, and adequate organ function. The calculated sample size was 350 with a one-sided α of 5%, a power of 80%, and non-inferiority margin hazard ratio (HR) of 1.155. The primary end point was OS, while the secondary end points included progression-free survival (PFS), response rate (RR), adverse events (AEs), and clinically significant AEs defined as grade ≥2 fatigue, anorexia, nausea, vomiting, oral mucositis, or diarrhea.
RESULTS
Between May 2013 and March 2016, 354 patients were enrolled. GS was found to be non-inferior to GC [median OS: 13.4 months with GC and 15.1 months with GS, HR, 0.945; 90% confidence interval (CI), 0.78-1.15; P = 0.046 for non-inferiority]. The median PFS was 5.8 months with GC and 6.8 months with GS (HR 0.86; 95% CI 0.70-1.07). The RR was 32.4% with GC and 29.8% with GS. Both treatments were generally well-tolerated. Clinically significant AEs were observed in 35.1% of patients in the GC arm and 29.9% in the GS arm.
CONCLUSIONS
GS, which does not require hydration, should be considered a new, convenient standard of care option for patients with advanced/recurrent BTC.
CLINICAL TRIAL NUMBER
This trial has been registered with the UMIN Clinical Trials Registry (http://www.umin.ac.jp/ctr/index.htm), number UMIN000010667.

Identifiants

pubmed: 31566666
pii: S0923-7534(20)32557-6
doi: 10.1093/annonc/mdz402
pii:
doi:

Substances chimiques

Drug Combinations 0
Deoxycytidine 0W860991D6
S 1 (combination) 150863-82-4
Tegafur 1548R74NSZ
Oxonic Acid 5VT6420TIG
Cisplatin Q20Q21Q62J
Gemcitabine 0

Banques de données

UMIN-CTR
['UMIN000010667']

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1950-1958

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

C Morizane (C)

Department of Hepatobiliary and Pancreatic Oncology, Tokyo. Electronic address: cmorizan@ncc.go.jp.

T Okusaka (T)

Department of Hepatobiliary and Pancreatic Oncology, Tokyo.

J Mizusawa (J)

JCOG Data Center/Operations Office, National Cancer Center Hospital, Tokyo.

H Katayama (H)

JCOG Data Center/Operations Office, National Cancer Center Hospital, Tokyo.

M Ueno (M)

Department of Gastroenterology, Hepatobiliary and Pancreatic Medical Oncology Division, Kanagawa Cancer Center, Yokohama.

M Ikeda (M)

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

M Ozaka (M)

Hepato-Biliary-Pancreatic Medicine Department, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo.

N Okano (N)

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

K Sugimori (K)

Gastroenterological Center, Yokohama City University Medical Center, Yokohama.

A Fukutomi (A)

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Shizuoka.

H Hara (H)

Department of Gastroenterology, Saitama Cancer Center, Saitama.

N Mizuno (N)

Department of Gastroenterology, Aichi Cancer Center Hospital, Nagoya.

H Yanagimoto (H)

Department of Surgery, Kansai Medical University Hospital, Hirakata.

K Wada (K)

Department of Surgery, Teikyo University School of Medicine, Tokyo.

K Tobimatsu (K)

Division of Gastroenterology, Department of Internal Medicine Kobe University Graduate School of Medicine, Kobe.

K Yane (K)

Center for Gastroenterology, Teine Keijinkai Hospital, Sapporo.

S Nakamori (S)

Department of Surgery, National Hospital Organization Osaka National Hospital, Osaka.

H Yamaguchi (H)

Department of Clinical Oncology, Jichi Medical University, Shimotsuke.

A Asagi (A)

Department of Gastrointestinal Medical Oncology, National Hospital Organization Shikoku Cancer Center, Matsuyama.

S Yukisawa (S)

Department of Medical Oncology, Tochigi Cancer Center, Utsunomiya.

Y Kojima (Y)

Department of Gastroenterology, National Center for Global Health and Medicine, Tokyo.

K Kawabe (K)

Department of Medicine and Bioregulatory Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka.

Y Kawamoto (Y)

Department of Gastroenterology and Hepatology, Hokkaido University Hospital, Sapporo.

R Sugimoto (R)

Department of Hepato-Biliary-Pancreatology, National Hospital Organization Kyushu Cancer Center, Fukuoka.

T Iwai (T)

Department of Gastroenterology, Kitasato University Hospital, Sagamihara.

K Nakamura (K)

Division of Gastroenterology, Chiba Cancer Center, Chiba.

H Miyakawa (H)

Department of Bilio-Pancreatology, Sapporo Kousei General Hospital, Sapporo.

T Yamashita (T)

Department of Gastroenterology, Kanazawa University, Kanazawa.

A Hosokawa (A)

Department of Gastroenterology and Hematology, University of Toyama, Faculty of Medicine, Toyama.

T Ioka (T)

Department of Cancer Survey and Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka.

N Kato (N)

Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba.

K Shioji (K)

Department of Internal medicine, Niigata Cancer Center Hospital, Niigata.

K Shimizu (K)

Department of Gastroenterology, Tokyo Women's Medical University, Tokyo.

T Nakagohri (T)

Gastroenterological Surgery, Tokai University School of Medicine, Isehara.

K Kamata (K)

Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka.

H Ishii (H)

Clinical Research Center, Chiba Cancer Center, Chiba, Japan.

J Furuse (J)

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

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