Study protocol for JCOG1807C (DEEP OCEAN): a interventional prospective trial to evaluate the efficacy and safety of durvalumab before and after operation or durvalumab as maintenance therapy after chemoradiotherapy against superior sulcus non-small cell lung cancer

Author:

Aokage Keiju1ORCID,Tsuboi Masahiro1,Zenke Yoshitaka2ORCID,Horinouchi Hidehito3ORCID,Nakamura Naoki4,Ishikura Satoshi5,Nishikawa Hiroyoshi6,Kumagai Shogo6,Koyama Shohei6,Kanato Keisuke7,Kataoka Tomoko7,Wakabayashi Masashi7,Fukutani Miki8,Fukuda Haruhiko7,Ohe Yuichiro3ORCID,Watanabe Shun-ichi9,

Affiliation:

1. Division of Thoracic Surgery, National Cancer Center Hospital East, Chiba

2. Division of Thoracic Oncology, National Cancer Center Hospital East, Chiba

3. Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo

4. Department of Radiology, St. Marianna University School of Medicine, Kawasaki, Kanagawa

5. Division of Radiology, Nagoya City University Hospital, Nagoya

6. Division of Cancer Immunology, Research Institute/Exploratory Oncology Research & Clinical Trial Center (EPOC), National Cancer Center, Tokyo, Chiba

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

8. Clinical Research Support Office, National Cancer Center Hospital East, Kashiwa, 277-8577

9. Division of Thoracic Surgery, National Cancer Center Hospital, Tokyo, Japan

Abstract

Abstract Background Superior sulcus tumours (SSTs) are relatively uncommon and one of the most intractable lung cancers among non-small cell lung cancer (NSCLC). We planned a multicenter, single-arm confirmatory trial of new multidisciplinary treatment using immune-checkpoint inhibitor. The aim is to evaluate the safety and efficacy of new multidisciplinary treatment with perioperative durvalumab after chemoradiotherapy (CRT). Methods The primary endpoint is 3-year overall survival. Patients receive induction CRT with sequential two courses of durvalumab, followed by surgical resection for resectable SST. The regimen for CRT is two courses of cisplatin and S-1, and concurrent radiotherapy (66 Gy/33 Fr). After surgery, 22 courses of post-operative durvalumab therapy are administered. For unresectable SST, an additional 22 courses of durvalumab are administered after induction durvalumab. Results In two cases as a safety cohort, the safety of intervention treatment up to 30 days after surgery was examined, and there were no special safety signals. Patient enrollment has now resumed in the main cohort. Conclusions The results of this study may contribute to the establishment of a new standard of care for SST, which is an intractable NSCLC.

Funder

National Cancer Center Research and Development Fund

Project Promoting Clinical Trials for Development of New Drugs

Japan Agency for Medical Research and Development

Publisher

Oxford University Press (OUP)

Subject

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

Reference6 articles.

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