The Fifth Medical Center, Chinese PLA General Hospital, Beijing, China.
Department of Gastrointestinal Oncology, Harbin Medical University Cancer Hospital, Harbin, China.
Expert Rev Anticancer Ther. 2022 Sep;22(9):981-998. doi: 10.1080/14737140.2022.2110470. Epub 2022 Aug 24.
There is no consensus on the optimal palliative first-line chemotherapy regimen for East Asian patients with advanced esophageal squamous cell carcinoma (ESCC).
We conducted a systematic review using a literature search of PubMed, Embase, and the Cochrane Library without date restrictions, and abstracts from major oncology congresses. Studies meeting the following criteria were included: East Asian patients ≥18 years old with metastatic/locally advanced unresectable ESCC; first-line chemotherapy; reporting of overall survival, progression-free survival, duration of response, overall response rate, and/or safety; randomized controlled trials, non-randomized controlled trials, and prospective or retrospective comparative studies. In total, 39 articles were identified for: platinum plus fluoropyrimidine (n = 9), platinum plus taxane (n = 16), platinum plus fluoropyrimidine plus taxane (n = 7), platinum plus fluoropyrimidine plus other (n = 3), irinotecan plus platinum (n = 2), taxane plus fluoropyrimidine (n = 1).
The available data supports both taxane plus platinum regimens and fluoropyrimidine plus platinum regimens in the first-line treatment of East Asian patients with ESCC. Compared with data from doublet chemotherapy studies, triplet chemotherapy appeared to improve ORR, but did not seem to prolong OS, possibly due to an increased incidence of adverse events.
对于东亚晚期食管鳞癌(ESCC)患者,尚无关于一线姑息化疗方案的共识。
我们对 PubMed、Embase 和 Cochrane 图书馆进行了系统检索,未设时间限制,并检索了主要肿瘤学大会的摘要,纳入了符合以下标准的研究:年龄≥18 岁的东亚转移性/局部晚期不可切除 ESCC 患者;一线化疗;报告总生存期、无进展生存期、缓解持续时间、总缓解率和/或安全性;随机对照试验、非随机对照试验和前瞻性或回顾性对照研究。共确定了 39 篇文章:铂类加氟嘧啶(n=9)、铂类加紫杉类(n=16)、铂类加氟嘧啶加紫杉类(n=7)、铂类加氟嘧啶加其他(n=3)、伊立替康加铂类(n=2)、紫杉类加氟嘧啶(n=1)。
现有数据支持紫杉类加铂类方案和氟嘧啶加铂类方案作为东亚 ESCC 患者的一线治疗。与双联化疗研究数据相比,三联化疗似乎提高了 ORR,但似乎并未延长 OS,这可能是由于不良反应发生率增加所致。