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低剂量化疗联合酪氨酸激酶抑制剂治疗费城染色体阳性急性淋巴细胞白血病的疗效与安全性

[The efficacy and safety of low-dose chemotherapy combined with tyrosine kinase inhibitors in the treatment of Philadelphia-chromosomal-positive acute lymphoblastic leukemia].

作者信息

Wang H, Zhao T, Hu L J, Li Z R, Jiang H, Qin Y Z, Lai Y Y, Shi H X, Huang X J, Jiang Q

机构信息

Beijing University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing 100044, China Wang Huan is working on the Beijing Chuiyangliu Hospital, Beijing 100021, China.

Beijing University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing 100044, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2022 Jul 14;43(7):550-556. doi: 10.3760/cma.j.issn.0253-2727.2022.07.004.

Abstract

The study aims to explore the efficacy and safety of low-dose chemotherapy combined with tyrosine kinase inhibitor (TKI) as an induction therapy for Philadelphia-chromosomal-positive acute lymphoblastic leukemia (Ph(+) ALL) . The data of the consecutive newly diagnosed patients with Ph(+) ALL were reviewed. The efficacy and safety of low-dose chemotherapy and conventional-dose chemotherapy combined with TKI were compared. A total of 217 patients with a median age of 38 (10-69) years old were included in this study. 78 patients were in the low-dose chemotherapy group, and 139 patients were in the conventional-dose chemotherapy group. There were no significant differences in the 4-week complete remission (CR) rate (98.7% 97.0%, =0.766) and overall CR rate (100% 100%, =1.000) between the two groups. Multivariate analyses showed that the chemotherapy intensity was not related to the disease-free survival rate and overall survival rate. However, the lower incidence of infection (=0.017) , the shorter duration of neutropenia (=0.001) and PLT<20 × 10(9)/L (=0.057) , and the lower red blood cell transfusion volume (=0.002) were more common in the low-dose chemotherapy group than in the conventional-dose chemotherapy group. The low-dose chemotherapy is superior to the conventional-dose chemotherapy combined with TKI as induction therapy in Ph(+) ALL with similar efficacy but is safer.

摘要

本研究旨在探讨低剂量化疗联合酪氨酸激酶抑制剂(TKI)作为费城染色体阳性急性淋巴细胞白血病(Ph(+) ALL)诱导治疗的疗效和安全性。回顾性分析了连续确诊的Ph(+) ALL患者的数据。比较了低剂量化疗和传统剂量化疗联合TKI的疗效和安全性。本研究共纳入217例患者,中位年龄为38岁(10 - 69岁)。低剂量化疗组78例,传统剂量化疗组139例。两组4周完全缓解(CR)率(98.7%对97.0%,P = 0.766)和总CR率(100%对100%,P = 1.000)差异无统计学意义。多因素分析显示,化疗强度与无病生存率和总生存率无关。然而,低剂量化疗组感染发生率较低(P = 0.017),中性粒细胞减少持续时间较短(P = 0.001),血小板<20×10⁹/L的持续时间较短(P = 0.057),红细胞输注量较低(P = 0.002)。在Ph(+) ALL诱导治疗中,低剂量化疗联合TKI与传统剂量化疗疗效相似,但安全性更好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6319/9395566/1dce61e4a892/cjh-43-07-550-g001.jpg

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