Zhang Guo-Cai, Zheng Dong, Li Qun-Hua, Li Xiao-Hu, Cai Cheng-Cai, Luo Shao-Kai, Li Juan, Peng Ai-Hua, Tong Xiu-Zhen, Tan En-Xun, Hong Wen-De
Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510080, P.R. China.
Ai Zheng. 2004 Dec;23(12):1696-9.
BACKGROUND & OBJECTIVE: Chronic myeloid leukemia (CML) in blast phase is refractory with a poor prognosis. This study was to evaluate efficacy of imatinib mesylate, a specific inhibitor of BCR/ABL tyrosine kinase, on CML in blast phase.
Nineteen patients with CML in blast phase (imatinib treatment group) received induction of cytarabine-based standard chemotherapy for 2 cycles, and 400 mg/d of imatinib mesylate for 4 weeks. Patients with no remission received 600 mg/d of imatinib mesylate for another 8 weeks. Treatment of 600 mg/d of imatinib mesylate was maintained if it showed effects after 8 weeks, otherwise it would be stopped. Twenty-two patients with CML in blast phase (historical control group) received inducement of cytarabine-based chemotherapy for 2 cycles, and other regimens of consolidation or continuous induction.
Sixteen patients of imatinib treatment group achieved no hematologic remission after induction. After treated with imatinib mesylate, 6 of 16 (38%) achieved hematologic complete remission (CHR), and major cytogenetic response; 2 of 16(13%) achieved hematologic partial remission (PHR); 1 of 16 (6%) returned to chronic phase with minor cytogenetic response. Total hematologic response rate of imatinib treatment group was 57%; 1-year survival rate was 38% (6/16). Eighteen patients of historical control group achieved no hematologic remission after inducement. After treated with other regimens, 2 (11%) achieved CHR, and 1 (6%) achieved PHR. Total hematologic response rate of historical control group was 17%; 1-year survival rate was 6%(1/18), significantly lower than that of imatinib treatment group (P< 0.05).
Imatinib mesylate may have anti-leukemic activity, and prolong survival time of patients with CML in blast phase. But problems of tumor relapse, and drug resistance are still present.
急变期慢性髓性白血病(CML)难治,预后差。本研究旨在评估BCR/ABL酪氨酸激酶特异性抑制剂甲磺酸伊马替尼对急变期CML的疗效。
19例急变期CML患者(伊马替尼治疗组)接受以阿糖胞苷为基础的标准化疗诱导2个周期,然后给予甲磺酸伊马替尼400mg/d,共4周。未缓解的患者再给予甲磺酸伊马替尼600mg/d,持续8周。若8周后显示有效,则维持600mg/d的甲磺酸伊马替尼治疗,否则停药。22例急变期CML患者(历史对照组)接受以阿糖胞苷为基础的化疗诱导2个周期,以及其他巩固或持续诱导方案。
伊马替尼治疗组16例患者诱导后未获得血液学缓解。接受甲磺酸伊马替尼治疗后,16例中的6例(38%)获得血液学完全缓解(CHR)及主要细胞遗传学反应;16例中的2例(13%)获得血液学部分缓解(PHR);16例中的1例(6%)回到慢性期并伴有微小细胞遗传学反应。伊马替尼治疗组的总血液学缓解率为57%;1年生存率为38%(6/16)。历史对照组18例患者诱导后未获得血液学缓解。接受其他方案治疗后,2例(11%)获得CHR,1例(6%)获得PHR。历史对照组的总血液学缓解率为17%;1年生存率为6%(1/18),显著低于伊马替尼治疗组(P<0.05)。
甲磺酸伊马替尼可能具有抗白血病活性,可延长急变期CML患者的生存时间。但仍存在肿瘤复发和耐药问题。