天津医药 ›› 2018, Vol. 46 ›› Issue (8): 819-823.doi: 10.11958/20180324

• 专题 临床研究 • 上一篇    下一篇

索拉菲尼单药治疗FLT3-ITD突变阴性和CD117高表达的复发/难治型急性髓系白血病临床观察

许剑辉1, 刘筱姝2 , 钟玉霞1 , 何颖芝1 , 杜静文1 , 黄宇贤1 , 李玉华1   

  1. 1南方医科大学珠江医院血液科 (邮编510282); 2广州市番禺中心医院血液科
  • 收稿日期:2018-03-06 修回日期:2018-07-17 出版日期:2018-08-15 发布日期:2018-08-23
  • 通讯作者: 许剑辉 E-mail:xujianhui_75@hotmail.com
  • 基金资助:
    广东省科技项目

The clinical observation of relapsed or refractory acute myeloid leukemia in patients with high CD117 expression but no FLT3-ITD mutation treated with sorafenib alone

XU Jian-hui 1, LIU Xiao-shu2 , ZHONG Yu-xia1 , HE Ying-zhi 1 , DU Jing-wen1 , HUANG Yu-xian1 , LI Yu-hua1   

  1. 1 Department of Hematology, Zhujiang Hospital of Southern Medical University, Guangzhou 510282, China; 2 Department of Hematology, Guangzhou Panyu Central Hospital
  • Received:2018-03-06 Revised:2018-07-17 Published:2018-08-15 Online:2018-08-23
  • Contact: Jianhui Xu E-mail:xujianhui_75@hotmail.com

摘要: 目的 初步分析索拉菲尼单药治疗FLT3-ITD突变阴性和CD117高表达的复发/难治型急性髓系白血病(R/R AML) 患者临床疗效。方法 回顾性分析7例高表达CD117但FLT3-ITD突变阴性的R/R AML患者应用索拉菲尼单药治疗后的临床反应和生存情况。治疗不良反应依据常见不良反应事件评价标准 (CTCAE) v4.0进行评估, 缓解标准依据NCCN指南确定。结果 7例患者中4例治疗获得缓解, 诱导完全缓解所需中位时间为36 d。索拉菲尼维持治疗过程中1例因皮疹疼痛中断治疗。3例对索拉菲尼治疗无反应者中2例接受挽救性移植治疗, 1例接受挽救性化疗, 均再度缓解。治疗期间, 1例出现1级肝脏不良反应, 1例出现3级皮损不良反应, 所有患者均有粒细胞缺乏 (> 7 d), 但未出现早期死亡。患者中位随访时间达到22个月, 3例缓解患者在索拉菲尼维持治疗后AML复发死亡, 其无病生存时间为2~20个月。无论索拉菲尼诱导治疗是否缓解, 接受了骨髓移植治疗的4例患者至今仍存活。7例患者的中位生存时间达650 d。结论 高表达CD117的R/R AML患者使用单药索拉菲尼治疗缓解表现较好, 有利于患者的长期生存。

关键词: 白血病, 髓样, 急性, 复发/难治, 索拉菲尼, CD117阴性, FLT3-ITD突变

Abstract: Objective To make a primary investigation of outcomes in relapsed or refractory (R/R) acute myeloid leukemia (AML) patients who were FLT3-ITD mutation negative and treated with sorafinib alone. Methods The clinical responses and survival of R/R AML patients who underwent sorafenib treatment only were retrospectively analyzed. The side effects and response results were assessed according to common terminology criteria for adverse events (CTCAE) v 4.0 from US National Institutes of Health and NCCN guideline. Results Four out of seven patients achieved complete remission by sorafenib treatment alone. The median time required for remission was 36 days in the four patients. Among them, only 1 patient stopped the maintenance treatment because of side effect of serious skin lesion. Three patients showed no response to sorafenib, including 2 accepted stem cell transplantation and 1 retrieved to salvage chemotherapy. All of them achieved complete remission later. One patient developed grade 1 adverse event of liver. Another one developed grade 3 skin lesion. All patients experienced neutropenia of more than 7 days without unendurable infections and early deaths. The median follow-up time for the whole cohort was more than 22 months. Three patients passed away for relapse of AML and their disease-free survival time with sorafenib ranged from 2 to 20 months. All four patients accepted stem cell transplantation were still surviving no matter whether or not they were responsive to sorafinib before. The median survival time for these seven patients was 650 days. Conclusion The R/R AML patients with negative FLT3-ITD mutation and high expression of CD117 treated with sorafenib alone have good remission and long term survival.

Key words: leukemia, myeloid, acute, relapsed/refractory, sorafenib, CD117 negative, FLT3-ITD mutation