Department of Head and Neck, Esophageal Medical Oncology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Department of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Esophagus. 2024 Jul;21(3):328-335. doi: 10.1007/s10388-024-01050-2. Epub 2024 Mar 12.
Chemotherapy consisting of 5-fluorouracil, leucovorin, oxaliplatin, and docetaxel is the standard perioperative treatment for resectable esophageal adenocarcinoma and esophagogastric junctional adenocarcinoma (EGJ-AC) in Western countries. Meanwhile, preoperative chemotherapy consisting of docetaxel, cisplatin, and 5-fluorouracil (DCF) has been developed for esophageal squamous cell carcinoma in Japan. However, there are few reports on the safety and efficacy of preoperative DCF for resectable EGJ-AC in the Japanese population.
Patients with histologically confirmed resectable EGJ-AC who received preoperative DCF (docetaxel 70 mg/m and cisplatin 70 mg/m on day 1 and continuous infusion of 5-fluorouracil 750 mg/m/day on days 1-5 every 3 weeks with a maximum of three cycles) between January 2015 and April 2020 were retrospectively evaluated. We assessed the rates of completion of ≥ 2 courses of DCF and R0 resection, histopathological response, progression-free survival (PFS), overall survival (OS), and adverse events.
Thirty-two patients were included. Median follow-up was 28.7 (range, 5.2-70.8) months and median age was 63 (range, 42-80) years. Twenty-one patients (66%) had a performance status of 0. The proportions of clinical stage IIA/IIB/III/IVA/IVB disease were 3%/0%/44%/44%/9%, respectively. The treatment completion rate was 84%. A histopathological response of grade 1a/1b/2/3 was obtained in 58%/26%/13%/3% of cases. Median PFS was 40.7 months (95% confidence interval 11.8-NA). Median OS was not reached (80.8% at 3 years). Grade ≥ 3 adverse events were observed in 63% of cases (neutropenia, 44%; febrile neutropenia, 13%). No treatment-related deaths occurred.
Preoperative DCF for resectable EGJ-AC was well tolerated and has promising efficacy.
在西方国家,氟尿嘧啶、亚叶酸、奥沙利铂和多西他赛组成的化疗方案是可切除食管腺癌和食管胃结合部腺癌(EGJ-AC)的标准围手术期治疗方法。同时,日本已经开发出了术前多西他赛、顺铂和氟尿嘧啶(DCF)化疗方案用于治疗食管鳞状细胞癌。然而,在日本人群中,关于可切除 EGJ-AC 的术前 DCF 的安全性和疗效的报道很少。
回顾性评估了 2015 年 1 月至 2020 年 4 月期间接受术前 DCF(多西他赛 70mg/m2 和顺铂 70mg/m2 于第 1 天,氟尿嘧啶 750mg/m2/天持续输注于第 1 天至第 5 天,每 3 周 1 个周期,最多 3 个周期)治疗的组织学证实可切除 EGJ-AC 患者的≥2 个疗程完成率和 R0 切除率、组织病理学反应、无进展生存期(PFS)、总生存期(OS)和不良事件发生率。
共纳入 32 例患者。中位随访时间为 28.7(5.2-70.8)个月,中位年龄为 63(42-80)岁。21 例(66%)患者的体能状态为 0。临床分期 IIA/IIB/III/IVA/IVB 疾病的比例分别为 3%/0%/44%/44%/9%。治疗完成率为 84%。1b/2/3 级组织病理学反应的比例分别为 58%/26%/13%/3%。中位 PFS 为 40.7 个月(95%置信区间 11.8-N/A)。中位 OS 未达到(3 年时为 80.8%)。≥3 级不良事件发生率为 63%(中性粒细胞减少症 44%;发热性中性粒细胞减少症 13%)。无治疗相关死亡。
可切除 EGJ-AC 的术前 DCF 耐受良好,疗效有前景。