Comparison between neoadjuvant chemotherapy followed by surgery and definitive chemoradiotherapy for survival in patients with resectable esophageal squamous cell carcinoma (JCOG2305A).
Abstract
417 Background: Neoadjuvant triplet chemotherapy followed by surgery (Neo-S) has become the standard treatment for resectable esophageal squamous cell carcinoma (ESCC) based on the results of JCOG1109. However, definitive chemoradiotherapy (CRT) remains an option for organ preservation with curative intent. This analysis aimed to explore subgroups of patients undergoing CRT, including salvage treatment, to identify those with survival outcomes potentially equivalent to Neo-S. Methods: Pooled data from two clinical trials of patients with resectable (T1N1-3M0 and T2-3NanyM0) ESCC. JCOG0909 was a single-arm trial that evaluated upfront CRT consisting of 5-FU (1000 mg/m 2 on day1-4, 29-32) and cisplatin (80 mg/m 2 on day1, 29) combined with radiotherapy at a dose of 50.4 Gy, including salvage treatment. If there was no progression at the time of salvage treatment, it was not regarded as an event for progression-free survival (PFS) in JCOG0909. JCOG1109 compared neoadjuvant treatment with doublet chemotherapy, triplet chemotherapy, and doublet chemotherapy with radiotherapy followed by surgery. The patients were enrolled in JCOG0909 between 2010 and 2014 and in JCOG1109 between 2012 and 2018. Subgroup analyses of clinical data, including tumor location, cT, cN, and clinical stage, were conducted on overall survival (OS) and PFS using Cox proportional hazards regression models for patients with JCOG0909 and JCOG1109. When a subgroup with a multivariable hazard ratio (HR) of more than 0.91 was detected, CRT including salvage treatment was considered not to be inferior to Neo-S in that subgroup. Results: Ninety-three patients in the CRT group from JCOG0909 and 196 patients in the Neo-S group from the triplet chemotherapy arm of JCOG1109 were included in this analysis. Although there were no significant differences, PFS and OS tend to be better in the Neo-S group than in the CRT group (PFS, HR 0.72, 95% confidence interval [CI] 0.50-1.03; OS, HR 0.89, 95% CI 0.59-1.36). For patients with Ut/Mt or cT1-2 disease, OS in the Neo-S group had a HR of 0.91 or more compared with those in the CRT group (Table). Conclusions: Subgroups in which OS after CRT including salvage treatment was not inferior to that of Neo-S were identified. Hazard ratios of Neo-S to CRT by subgroups in multivariable Cox regression. Progression-free survival Overall survival Subgroups Hazard ratio 95% confidence interval Hazard ratio 95% confidence interval Ut/Mt 0.85 0.56-1.28 1.13 0.70-1.83 Lt 0.45 0.21-0.97 0.44 0.19-1.00 cT1-2 0.88 0.46-1.68 1.45 0.65-3.24 cT3 0.66 0.42-1.02 0.72 0.44-1.16 cStage IB+II 0.79 0.45-1.36 1.06 0.56-2.00 cStage III 0.75 0.45-1.23 0.92 0.52-1.62 Overall 0.72 0.50-1.03 0.89 0.59-1.36 Ut upper thoracic esophagus, Mt middle thoracic esophagus, Lt lower thoracic esophagus.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Motoo Nomura
Tomohiro Kadota
Department of Gastroenterology and Endoscopy, National Cancer Center Hospital East, Kashiwa, Japan
Ken Kato
Institute for Protein Research, The University of Osaka, 3-2 Yamadaoka, Suita-shi, Osaka 565-0871, Japan
Ryunosuke Machida
2JCOG Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan
Ryosuke Kita
Department of Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan
Yoshinori Ito
Yuko Kitagawa
Hiroyuki Daiko
Department of Esophageal Surgery, National Cancer Center Hospital, Tokyo, Japan
Yasuhiro Tsubosa
Division of Esophageal Surgery, Shizuoka Cancer Center, Shizuoka, Japan
Yoshiaki Nagatani
Department of Medical Oncology and Hematology, Kobe University Hospital, Kobe-Shi Chuo-Ku, Japan
Hiroki Hara
Saitama Cancer Center, Ina, Japan
Keiko Minashi
Department of Gastroenterology, Chiba Cancer Center, Chiba, Japan
Takeshi Kajiwara
Shikoku Cancer Center, Matsuyama-Shi, Japan
Kazuo Koyanagi
Department of Gastroenterological Surgery, Tokai University School of Medicine, Isehara, Japan
Takashi Ogata
Department of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama, Japan
Takako Yoshii
Takeo Fujita
Department of Esophageal Surgery, National Cancer Center Hospital East, Kashiwa, Japan
Satoru Matsuda
Department of Surgery, Keio University School of Medicine, Tokyo, Japan
Takahiro Tsushima
Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Shizuoka, Japan
Hiroya Takeuchi