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甲磺酸伊马替尼(STI571)治疗急变期费城染色体阳性慢性粒细胞白血病。

Imatinib mesylate (STI571) therapy for Philadelphia chromosome-positive chronic myelogenous leukemia in blast phase.

作者信息

Kantarjian Hagop M, Cortes Jorge, O'Brien Susan, Giles Francis J, Albitar Maher, Rios Mary Beth, Shan Jianqin, Faderl Stefan, Garcia-Manero Guillermo, Thomas Deborah A, Resta Debra, Talpaz Moshe

机构信息

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Blood. 2002 May 15;99(10):3547-53. doi: 10.1182/blood.v99.10.3547.

Abstract

Molecular abnormalities caused by the hybrid Bcr-Abl gene are causally associated with the development and progression of Philadelphia chromosome-positive (Ph(+)) chronic myelogenous leukemia (CML). Imatinib mesylate (STI571), a specific Bcr-Abl tyrosine-kinase signal-transduction inhibitor, has shown encouraging activity in phase I and II studies of CML. Here, we describe the use of imatinib mesylate to treat 75 patients in blast-phase CML (median age, 53 years; 65 with nonlymphoid and 10 with lymphoid blasts), and compare the results with those of a historical control group treated with standard cytarabine-based therapy. Imatinib mesylate was given as oral doses at 300 to 1000 mg per day and was the first salvage therapy for 47 patients. The objective response rate was 52% (39 of 75 patients: 16 had complete and 3 had partial hematologic response; 12 had hematologic improvement; 7 returned to second chronic phase; and 1 had a complete response in extramedullary blastic disease). Response rates were not different between nonlymphoid and lymphoid groups. The cytogenetic response rate was 16% (12 patients: 5 complete, 3 partial [Ph(+) below 35%], and 4 minor [Ph(+), 34% to 90%]). The estimated median overall survival was 6.5 months; the estimated 1-year survival was 22%. Response to therapy (landmark analysis at 8 weeks) was associated with survival prolongation. Compared with standard cytarabine combinations, imatinib mesylate therapy was less toxic and produced a higher response rate (55% versus 29%, P =.001), longer median survival (7 versus 4 months, P =.04), and lower 4-week induction mortality (4% versus 15%, P =.07). Imatinib mesylate is currently being tested in combination with other drugs to improve the prognosis for blast-phase CML.

摘要

由杂交Bcr-Abl基因引起的分子异常与费城染色体阳性(Ph(+))慢性粒细胞白血病(CML)的发生和进展存在因果关系。甲磺酸伊马替尼(STI571)是一种特异性Bcr-Abl酪氨酸激酶信号转导抑制剂,在CML的I期和II期研究中已显示出令人鼓舞的活性。在此,我们描述了使用甲磺酸伊马替尼治疗75例急变期CML患者(中位年龄53岁;65例为非淋巴细胞性急变,10例为淋巴细胞性急变),并将结果与接受基于阿糖胞苷的标准治疗的历史对照组进行比较。甲磺酸伊马替尼口服剂量为每日300至1000 mg,是47例患者的首次挽救治疗。客观缓解率为52%(75例患者中的39例:16例完全缓解,3例部分血液学缓解;12例血液学改善;7例恢复至第二次慢性期;1例髓外原始细胞疾病完全缓解)。非淋巴细胞性和淋巴细胞性组的缓解率无差异。细胞遗传学缓解率为16%(12例患者:5例完全缓解,3例部分缓解[Ph(+)低于35%],4例微小缓解[Ph(+),34%至90%])。估计的中位总生存期为6.5个月;估计的1年生存率为22%。治疗反应(8周时的标志性分析)与生存期延长相关。与标准阿糖胞苷联合治疗相比,甲磺酸伊马替尼治疗毒性较小,缓解率更高(55%对29%,P = 0.001),中位生存期更长(7个月对4个月,P = 0.04),4周诱导死亡率更低(4%对15%,P = 0.07)。目前正在对甲磺酸伊马替尼与其他药物联合使用进行试验,以改善急变期CML的预后。

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