TY - JOUR
T1 - A Single-Arm Confirmatory Study of Definitive Chemoradiation Therapy Including Salvage Treatment for Clinical Stage II/III Esophageal Squamous Cell Carcinoma (JCOG0909 Study)
AU - Japan Esophageal Oncology Group of the Japan Clinical Oncology Group
AU - Takeuchi, Hiroya
AU - Ito, Yoshinori
AU - Machida, Ryunosuke
AU - Kato, Ken
AU - Onozawa, Masakatsu
AU - Minashi, Keiko
AU - Yano, Tomonori
AU - Nakamura, Kenichi
AU - Tsushima, Takahiro
AU - Hara, Hiroki
AU - Okuno, Tatsuya
AU - Hironaka, Shuichi
AU - Nozaki, Isao
AU - Ura, Takashi
AU - Chin, Keisho
AU - Kojima, Takashi
AU - Seki, Shiko
AU - Sakanaka, Katsuyuki
AU - Fukuda, Haruhiko
AU - Kitagawa, Yuko
N1 - Funding Information:
The study was supported in part by the National Cancer Center Research and Development Funds (20S-3, 23-A-19, 26-A-4, 29-A-3).
Funding Information:
Disclosures: H.T. reports grants and personal fees from Taiho Pharmaceutical, Chugai Pharma, Otsuka Pharmaceutical Factory, Eli Lilly, Daiichi Sankyo Company, Ltd, EA Pharma, Tsumura, ONO Pharmaceutical, and Kaken Pharmaceutical; grant fees from Shionogi, Astellas Pharma, Bayer Yakuhin, Sanofi, MSD, Novartis Pharma, Takeda Pharmaceutical, and Nippon Kayaku; and personal fees from Covidien Japan, Johnson & Johnson, Olympus Medical Systems Corp, Abbott Japan, Asahikasei Pharma, and Pfizer, outside the submitted work. Y.I. reports personal fees from Chugai Pharma, Ono Pharmaceutical, Taiho Pharmaceutical, Bristol-Myers Squibb Japan, AstraZeneca, Oncolys BioPharma, and Eisai, outside the submitted work. K.K. reports grant fees from Ono Pharmaceutical, MSD, Beigene, Shionogi, Oncolys BioPharma, AstraZeneca, Bayer, and Chugai Pharma, outside the submitted work. K.M. reports grant fees from Ono Pharmaceutical, MSD, Mediscience Planning, Merck Biopharma, Astellas Pharm, Taiho Pharmaceutical, Daiichi Sankyo, Yakult Honsha, Merk, and Bayer, outside the submitted work. T.T. reports personal fees from Ono Pharmaceutical, Taiho Pharma, Eli Lilly, Takeda Pharmaceutical, Yakult Honsha, Merk, and Bayer, outside the submitted work. H.H. reports grants and personal fees from AstraZeneca, Daiichi Sankyo, Dainippon Sumitomo Pharma, Merck Biopharma, MSD, Taiho Pharmaceutical, Chugai Pharma, Boehringer Ingelheim, Ono Pharmaceutical, and Bristol-Myers Squibb Japan; grant fees from Eisai, Elevar Therapeutics, Incyte, Pfizer, Beigene, and Astellas; and personal fees from Lilly, Yakult Honsha, Sanofi, Takeda, and Kyowa Hakko Kirin, outside the submitted work. S.H. reports grants and personal fees from Ono Pharmaceutical, Taiho Pharmaceutical, Chugai Pharma, and AstraZeneca; grant fees from Sanofi, Pfizer, Boehringer Ingelheim, Toyama Chemical Co, Kyowa Hakko Kirin, Astellas Pharma, Yakult Honsha, Shionogi, and Takeda; and personal fees from Bristol-Myers Squibb Japan, Daiichi Sankyo, Lilly, Nihonkayaku, Tsumura & Co, Sanofi, and Merck, outside the submitted work. K.C. reports personal fees from Ono Pharmaceutical, Taiho Pharmaceutical, and Chugai Pharma, outside the submitted work. T.K. reports grants and personal fees from Ono Pharmaceutical, MSD, and Astellas Amgen Pharma; grant fees from Amgen BioPharma, Taiho Pharmaceutical, and Shionogi; and personal fees from Oncolys BioPharma, Bristol-Myers Squibb Japan, and Merk, outside the submitted work. Y.K. reports grants and personal fees from Asahi Kasei Pharma Corporation, Taiho Pharmaceutical, Chugai Pharma, EA Pharma, Yakult Honsha, Otsuka Pharmaceutical, Otsuka Pharmaceutical Factory, Astellas Pharma, Dainippon Sumitomo Pharma, Toyama Chemical, Ono Pharmaceutical, and Nihon Pharmaceutical; grant fees from Takeda Pharmaceutical, Kaken Pharmaceutical, Medicon, Kyouwa Hakkou Kirin, Tsumura & Co, FUJIFILM Toyama Chemical, Nippon Covidien, Eisai, and Teijin Pharma Ltd; and personal fees from Shionogi, outside the submitted work. All other authors have no disclosures to declare.
Publisher Copyright:
© 2022 Elsevier Inc.
PY - 2022/11/1
Y1 - 2022/11/1
N2 - Purpose: Definitive chemoradiotherapy (CRT) is the standard treatment for patients with locally advanced esophageal cancer (EC) who refuse surgery as the initial therapy. However, poor survival, a high incidence of late toxicities, and severe complications after salvage surgery remain issues to be resolved. This single-arm multicenter trial (JCOG0909) aimed to confirm the efficacy of CRT modifications, including salvage treatment for reducing CRT-related toxicities and facilitating salvage treatment for improved survival. Methods and Materials: Patients with clinical stage II/III EC (International Union Against Cancer sixth edition, non-T4) were eligible. Chemotherapy comprised cisplatin (75 mg/m2 on days 1 and 29) and 5-fluorouracil (1000 mg/m2/d on days 1-4 and 29-32). Radiation therapy was administered at a total dose of 50.4 Gy. Good responders received 1 to 2 additional cycles of chemotherapy. For residual or recurrent disease, salvage endoscopic resection or salvage surgery was performed based on specific criteria. The primary endpoint was 3-year overall survival (OS). The calculated sample size was 95 patients, with a 1-sided alpha of 5% and a power of 80%. The expected and threshold 3-year OS were 55% and 42%, respectively. Results: Overall, 96 patients were enrolled, and 94 were included in the efficacy analysis. A complete response was achieved in 55 patients (59%). Salvage endoscopic resection and salvage surgery were performed in 5 (5%) and 25 patients (27%), respectively. R0 resection by salvage surgery was achieved in 19 patients (76%). Five patients (20%) showed grade 3 or 4 early operative complications, and 9 patients (9.6%) showed grade 3 late toxicities during the long-term follow-up. The 3-year OS was 74.2% (90% confidence interval, 65.9%-80.8%). Conclusion: The combination of definitive CRT and salvage treatment has lower CRT-related toxicities and yields good OS, thus making it a promising novel treatment option for patients with locally advanced EC.
AB - Purpose: Definitive chemoradiotherapy (CRT) is the standard treatment for patients with locally advanced esophageal cancer (EC) who refuse surgery as the initial therapy. However, poor survival, a high incidence of late toxicities, and severe complications after salvage surgery remain issues to be resolved. This single-arm multicenter trial (JCOG0909) aimed to confirm the efficacy of CRT modifications, including salvage treatment for reducing CRT-related toxicities and facilitating salvage treatment for improved survival. Methods and Materials: Patients with clinical stage II/III EC (International Union Against Cancer sixth edition, non-T4) were eligible. Chemotherapy comprised cisplatin (75 mg/m2 on days 1 and 29) and 5-fluorouracil (1000 mg/m2/d on days 1-4 and 29-32). Radiation therapy was administered at a total dose of 50.4 Gy. Good responders received 1 to 2 additional cycles of chemotherapy. For residual or recurrent disease, salvage endoscopic resection or salvage surgery was performed based on specific criteria. The primary endpoint was 3-year overall survival (OS). The calculated sample size was 95 patients, with a 1-sided alpha of 5% and a power of 80%. The expected and threshold 3-year OS were 55% and 42%, respectively. Results: Overall, 96 patients were enrolled, and 94 were included in the efficacy analysis. A complete response was achieved in 55 patients (59%). Salvage endoscopic resection and salvage surgery were performed in 5 (5%) and 25 patients (27%), respectively. R0 resection by salvage surgery was achieved in 19 patients (76%). Five patients (20%) showed grade 3 or 4 early operative complications, and 9 patients (9.6%) showed grade 3 late toxicities during the long-term follow-up. The 3-year OS was 74.2% (90% confidence interval, 65.9%-80.8%). Conclusion: The combination of definitive CRT and salvage treatment has lower CRT-related toxicities and yields good OS, thus making it a promising novel treatment option for patients with locally advanced EC.
UR - http://www.scopus.com/inward/record.url?scp=85137978023&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85137978023&partnerID=8YFLogxK
U2 - 10.1016/j.ijrobp.2022.07.007
DO - 10.1016/j.ijrobp.2022.07.007
M3 - Article
C2 - 35932949
AN - SCOPUS:85137978023
SN - 0360-3016
VL - 114
SP - 454
EP - 462
JO - International Journal of Radiation Oncology Biology Physics
JF - International Journal of Radiation Oncology Biology Physics
IS - 3
ER -