Literature DB >> 33375499

Progress in Multimodal Treatment for Advanced Esophageal Squamous Cell Carcinoma: Results of Multi-Institutional Trials Conducted in Japan.

Kazuo Koyanagi1, Kohei Kanamori1, Yamato Ninomiya1, Kentaro Yatabe1, Tadashi Higuchi1, Miho Yamamoto1, Kohei Tajima1, Soji Ozawa1.   

Abstract

In Japan, the therapeutic strategies adopted for esophageal carcinoma are based on the results of multi-institutional trials conducted by the Japan Esophageal Oncology Group (JEOG), a subgroup of the Japan Clinical Oncology Group (JCOG). Owing to the differences in the proportion of patients with squamous cell carcinoma among all patients with esophageal carcinoma, chemotherapeutic drugs available, and surgical procedures employed, the therapeutic strategies adopted in Asian countries, especially Japan, are often different from those in Western countries. The emphasis in respect of postoperative adjuvant therapy for patients with advanced esophageal squamous cell carcinoma (ESCC) shifted from postoperative radiotherapy in the 1980s to postoperative chemotherapy in the 1990s. In the 2000s, the optimal timing of administration of perioperative adjuvant chemotherapy returned from the postoperative adjuvant setting to the preoperative neoadjuvant setting. Recently, the JEOG commenced a three-arm randomized controlled trial of neoadjuvant therapies (cisplatin + 5-fluorouracil (CF) vs. CF + docetaxel (DCF) vs. CF + radiation therapy (41.4 Gy) (CRT)) for localized advanced ESCC, and patient recruitment has been completed. Salvage and conversion surgeries for ESCC have been developed in Japan, and the JEOG has conducted phase I/II trials to confirm the feasibility and safety of such aggressive surgeries. At present, the JEOG is conducting several trials for patients with resectable and unresectable ESCC, according to the tumor stage. Herein, we present a review of the JEOG trials conducted for advanced ESCC.

Entities:  

Keywords:  definitive chemoradiotherapy; esophageal squamous cell carcinoma; multimodal treatment; neoadjuvant chemoradiotherapy; neoadjuvant chemotherapy

Year:  2020        PMID: 33375499     DOI: 10.3390/cancers13010051

Source DB:  PubMed          Journal:  Cancers (Basel)        ISSN: 2072-6694            Impact factor:   6.639


  4 in total

1.  Significance of intratreatment tumor volume change during chemoradiotherapy for potentially resectable thoracic esophageal squamous cell carcinoma.

Authors:  Duojie Li; Qun Zhang; Yan Yang; Hongmei Yin; Chaomang Zhu; Xianming Li
Journal:  Am J Transl Res       Date:  2022-07-15       Impact factor: 3.940

2.  HMGB1 induces radioresistance through PI3K/AKT/ATM pathway in esophageal squamous cell carcinoma.

Authors:  Xueyuan Zhang; Naiyi Zou; Wenzhao Deng; Chunyang Song; Ke Yan; Wenbin Shen; Shuchai Zhu
Journal:  Mol Biol Rep       Date:  2022-10-19       Impact factor: 2.742

3.  The Sequence of Chemotherapy and Toripalimab Might Influence the Efficacy of Neoadjuvant Chemoimmunotherapy in Locally Advanced Esophageal Squamous Cell Cancer-A Phase II Study.

Authors:  Wenqun Xing; Lingdi Zhao; Yan Zheng; Baoxing Liu; Xianben Liu; Tiepeng Li; Yong Zhang; Baozhen Ma; Yonghao Yang; Yiman Shang; Xiaomin Fu; Guanghui Liang; Dongfeng Yuan; Jinrong Qu; Xiaofei Chai; He Zhang; Zibing Wang; Hongwei Lin; Liang Liu; Xiubao Ren; Jiangong Zhang; Quanli Gao
Journal:  Front Immunol       Date:  2021-12-06       Impact factor: 7.561

4.  LncRNA SNHG16 promotes development of oesophageal squamous cell carcinoma by interacting with EIF4A3 and modulating RhoU mRNA stability.

Authors:  Lihua Ren; Xin Fang; Sachin Mulmi Shrestha; Qinghua Ji; Hui Ye; Yan Liang; Yang Liu; Yadong Feng; Jingwu Dong; Ruihua Shi
Journal:  Cell Mol Biol Lett       Date:  2022-10-11       Impact factor: 8.702

  4 in total

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