Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.
Department of Digestive, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, China.
Sci Prog. 2024 Oct-Dec;107(4):368504241299016. doi: 10.1177/00368504241299016.
At present, albumin-bound paclitaxel combined with platinum is the standard first-line treatment option for advanced esophageal cancer (EC). However, following a hospitalization surge, clinicians may prefer to use albumin-bound paclitaxel as a single dose. The present study aimed to investigate the survival of patients with advanced EC when treated with single or fractionated doses of albumin-bound paclitaxel.
We collected survival data of patients with advanced first-line EC who had used albumin-bound paclitaxel with or without other treatment regimens from January 2018 to September 2023 at the Harbin Medical University Cancer Hospital and the Shanxi Province Cancer Hospital. The patients were divided into two groups according to the frequency and dose of albumin-bound paclitaxel administration, namely the abraxane fractional administration group (A group, 27 patients) and the abraxane single administration group (B group, 182 patients).
The median progression-free survival (PFS) was 9.0 months in both groups ( = 0.35), and the median overall survival (OS) was 21.0 months in A group and 18.0 months in B group ( = 0.61). The objective response rate was 37% in A group and 25% in B group ( = 0.314), and the disease control rate was 89% in A group and 83% in B group ( = 0.580). The incidence of grade 3 or higher treatment-related adverse events was 15% in both groups.
Albumin-bound paclitaxel treatments showed no statistically significant differences in the PFS or OS. They were considered safe, whether administered as a single dose or in fractionated doses.
目前,白蛋白结合紫杉醇联合铂类是晚期食管癌(EC)的标准一线治疗选择。然而,在住院人数激增后,临床医生可能更倾向于使用白蛋白结合紫杉醇作为单剂量治疗。本研究旨在探讨晚期 EC 患者使用单剂量或分剂量白蛋白结合紫杉醇治疗的生存情况。
我们收集了 2018 年 1 月至 2023 年 9 月在哈尔滨医科大学附属肿瘤医院和山西省肿瘤医院接受白蛋白结合紫杉醇联合或不联合其他治疗方案的一线晚期 EC 患者的生存数据。根据白蛋白结合紫杉醇给药的频率和剂量,患者分为两组,即白蛋白结合紫杉醇分次给药组(A 组,27 例)和白蛋白结合紫杉醇单次给药组(B 组,182 例)。
两组患者的中位无进展生存期(PFS)均为 9.0 个月(P=0.35),中位总生存期(OS)A 组为 21.0 个月,B 组为 18.0 个月(P=0.61)。A 组客观缓解率为 37%,B 组为 25%(P=0.314),疾病控制率 A 组为 89%,B 组为 83%(P=0.580)。两组治疗相关不良事件发生率均为 3%。
白蛋白结合紫杉醇治疗在 PFS 或 OS 方面无统计学差异。无论是单剂量还是分剂量使用,均被认为是安全的。