Ji Yongling, Du Xianghui, Tian Ye, Sheng Liming, Cheng Lei, Chen Ying, Qiu Guoqing, Zhou Xia, Bao Wuan, Zhang Danhong, Chen Ming
Department of Radiotherapy and Oncology, The Second Affiliated Hospital of Soochow University, 215000 Suzhou, China.
Department of Radiation Oncology, Zhejiang Cancer Hospital, 310022 Hangzhou, China.
Oncotarget. 2017 Sep 15;8(47):83022-83029. doi: 10.18632/oncotarget.20938. eCollection 2017 Oct 10.
Concurrent chemoradiotherapy (CCRT) using conventional platinum-based doublets are often associated with significant incidence of toxic effects in elderly patients with esophageal cancer. We previously reported a phase I trial of CCRT using S-1, an oral 5-fluorouracil derivative, which yielded well safe and active outcomes.
Patients with histologically confirmed esophageal cancer, who were age of 70 years or older with performance status (PS) score of 0-2 or age of 66 to 69 with PS score of 2, were eligible for this Phase II trial. Radiotherapy was delivered in 1.8 Gy per fraction to a total dose of 54 Gy. Concurrently, S-1 was administered at 70 mg/m on days 1-14 and 29-42. The primary end point was 2-year overall survival rate.
Thirty patients were enrolled, and 28 patients completed the full course of radiotherapy. No grade 4 toxicity or treatment-related death occurred. The grade 3 toxicities included esophagitis (16.7%), leucopoenia (13.3%), neutropenia (10%), anaemia (3.3%), pneumonitis (3.3%) and fatigue (3.3%). The median progression-free survival time and median survival time was 19 and 24 months, respectively. The 2-year overall survival rate was 45.1%, which exceeded the predefined threshold of 2-year OS 35% and met the primary end point of the study.
The results suggest that CCRT using S-1 is effective with mild toxicity in elderly patients with esophageal cancer. A phase III trial is needed to further evaluate this regimen.
在老年食管癌患者中,使用传统铂类双联化疗方案的同步放化疗(CCRT)常常伴随着较高的毒副反应发生率。我们之前报道了一项使用口服5-氟尿嘧啶衍生物S-1进行CCRT的I期试验,该试验取得了良好的安全性和有效性结果。
组织学确诊为食管癌、年龄70岁及以上且体能状态(PS)评分为0-2分,或年龄66至69岁且PS评分为2分的患者符合本II期试验入组条件。放疗每次剂量为1.8 Gy,总剂量为54 Gy。同时,在第1-14天和第29-42天给予S-1,剂量为70 mg/m²。主要终点为2年总生存率。
共入组30例患者,28例患者完成了全程放疗。未发生4级毒性反应或与治疗相关的死亡。3级毒性反应包括食管炎(16.7%)、白细胞减少(13.3%)、中性粒细胞减少(10%)、贫血(3.3%)、肺炎(3.3%)和疲劳(3.3%)。中位无进展生存时间和中位生存时间分别为19个月和24个月。2年总生存率为45.1%,超过了预先设定的2年总生存率35%的阈值,达到了研究的主要终点。
结果表明,在老年食管癌患者中,使用S-1的CCRT疗效显著且毒性轻微。需要进行III期试验以进一步评估该方案。