Phase III study of tri-modality combination therapy with induction docetaxel plus cisplatin and 5-fluorouracil versus definitive chemoradiotherapy for locally advanced unresectable squamous-cell carcinoma of the thoracic esophagus (JCOG1510: TRIANgLE)

Author:

Terada Mitsumi12,Hara Hiroki3,Daiko Hiroyuki4,Mizusawa Junki5,Kadota Tomohiro5ORCID,Hori Keisuke6,Ogawa Hirofumi7,Ogata Takashi8,Sakanaka Katsuyuki9,Sakamoto Takeshi10,Kato Ken11,Kitagawa Yuko12

Affiliation:

1. International Trials Management Section, Clinical Research Support Office, National Cancer Center Hospital, Japan

2. Medical Department, EORTC Headquarters, Belgium

3. Department of Gastroenterology, Saitama Cancer Center, Saitama

4. Esophageal Surgery Division, National Cancer Center Hospital, Japan

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

6. Department of Gastroenterology and Endoscopy, National Cancer Center Hospital East, Kashiwa, Chiba

7. Division of Radiation Oncology, Shizuoka Cancer Center, Shizuoka

8. Department of Gastrointestinal Surgery, Kanagawa Cancer Center, Kanagawa

9. Department of Radiation Oncology and Image-Applied Therapy, Graduate School of Medicine, Kyoto University

10. Department of Gastroenterology, Hyogo Cancer Center

11. Gastrointestinal Medical Oncology Division, National Cancer Center Hospital, Tokyo

12. Department of Surgery, Keio University School of Medicine, Tokyo, Japan

Abstract

Abstract A randomized phase III trial commenced in Japan in February 2018. Definitive chemoradiotherapy (CRT) with cisplatin plus 5-fluorouracil is the current standard treatment for locally advanced unresectable esophageal carcinoma. The purpose of this study is to confirm the superiority of induction chemotherapy with docetaxel plus cisplatin and 5-fluorouracil (DCF) followed by conversion surgery or definitive CRT over definitive CRT alone for overall survival (OS) in patients with locally advanced unresectable squamous-cell carcinoma of thoracic esophagus. A total of 230 patients will be accrued from 47 Japanese institutions over 4.5 years. The primary endpoint is OS, and the secondary endpoints are progression-free survival, complete response rate of CRT, response rate of DCF, adverse events of DCF and CRT, late adverse events and surgical complications. This trial has been registered at the Japan Registry of Clinical Trials as jRCTs031180181.

Funder

Japan Agency for Medical Research and Development

National Cancer Center Research and Development Fund

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Radiology Nuclear Medicine and imaging,Oncology,General Medicine

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