A multicenter randomized controlled trial of esophagectomy with or without prophylactic supraclavicular node dissection: a phase 3 trial (JCOG2013, MODERN3)

Author:

Tsunoda Shigeru1ORCID,Tsubosa Yasuhiro2,Sasaki Keita3,Machida Ryunosuke3,Kita Ryosuke3,Fukuda Haruhiko3,Koyanagi Kazuo4,Takeuchi Hiroya5,Kamei Takashi6,Mine Shinji7,Noma Kazuhiro8,Kato Ken9ORCID,Kitagawa Yuko10,

Affiliation:

1. Department of Surgery, Graduate School of Medicine, Kyoto University , Kyoto

2. Division of Esophageal Surgery, Shizuoka Cancer Center , Shizuoka

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

4. Department of Gastroenterological Surgery, Tokai University School of Medicine , Isehara

5. Department of Surgery, Hamamatsu University School of Medicine , Hamamatsu

6. Department of Surgery, Tohoku University Graduate School of Medicine , Sendai

7. Department of Esophageal and Gastroenterological Surgery, Juntendo University Graduate School of Medicine , Tokyo

8. Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine , Okayama

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

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

Abstract

Abstract The need for prophylactic supraclavicular lymph node dissection during esophagectomy with radical lymphadenectomy remains controversial. A randomized phase III trial was launched in August 2022 to confirm the non-inferiority of esophagectomy with D2 lymphadenectomy except for supraclavicular lymph node dissection to standard D2 lymphadenectomy in terms of overall survival for patients with resectable upper or middle thoracic esophageal cancer. This study will enroll 480 patients from 54 Japanese institutions over 5 years. The primary endpoint includes overall survival, and the secondary endpoints include relapse-free survival, perioperative and late complication incidences, supraclavicular lymph node recurrence, salvage cervical treatment incidence, synchronous cervical and abdominal procedure proportion, operation time and the number of operating surgeons. This trial has been registered at the Japan Registry of Clinical Trials under study number jRCT1030220248.

Funder

National Cancer Center Research and Development Funds

Japan Agency for Medical Research and Development

Publisher

Oxford University Press (OUP)

Subject

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

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