Sharma Atul, Bahl Ankur, Raina Vinod, Kumar Lalit, Gupta Ritu
Department of Medical Oncology Laboratory Oncology, Dr B. R. A. Institute Rotary Cancer Hospital, All India Institute of Medical Sciences, New Delhi 110029, India.
Asia Pac J Clin Oncol. 2012 Dec;8(4):375-9. doi: 10.1111/j.1743-7563.2012.01557.x. Epub 2012 Jul 6.
To report our experience of the use of dasatinib in various phases of chronic myeloid leukemia (CML).
Ten patients in various phases of CML, not responding to imatinib and started on dasatinib, were included and analyzed. The baseline characteristics of the patients and their salient features including the duration and response to initial therapy as well as to dasatinib, were noted.
Before starting dasatinib three patients were in chronic phase of CML while seven others were in the progressive phase (accelerated and blast phase) of CML. Half the patients developed transient grade 3 and 4 toxicities to dasatinib. Overall, the tolerability of the drug in all 10 patients was acceptable and none discontinued treatment. Three patients died due to progressive disease while the remaining seven are continuing the drug with the disease still under cytogenetic or hematological remission. Of the 10 patients, seven achieved complete hematological response and two of the accelerated phase/blast crisis patients achieved complete cytogenetic response. Overall, dasatinib was able to control disease for a median of 20.6 months.
Despite small sample size and insufficient information on mutational analysis, dasatinib is effective in CML in India. Cost limits the use of second-generation tyrosine kinase inhibitors in India. Our observation is not suitable for survival analysis but the difference made by dasatinib in progressive disease and its tolerability needs to be acknowledged.
报告我们在慢性髓性白血病(CML)各阶段使用达沙替尼的经验。
纳入并分析了10例处于CML各阶段、对伊马替尼无反应且开始使用达沙替尼的患者。记录患者的基线特征及其显著特征,包括初始治疗以及达沙替尼治疗的持续时间和反应。
开始使用达沙替尼之前,3例患者处于CML慢性期,另外7例处于CML进展期(加速期和急变期)。一半患者出现了对达沙替尼的3级和4级短暂毒性反应。总体而言,所有10例患者对该药物的耐受性均可接受,无一例中断治疗。3例患者因疾病进展死亡,其余7例继续使用该药物,疾病仍处于细胞遗传学或血液学缓解状态。10例患者中,7例实现了完全血液学缓解,2例加速期/急变期患者实现了完全细胞遗传学缓解。总体而言,达沙替尼能够将疾病控制中位时间为20.6个月。
尽管样本量小且关于突变分析的信息不足,但达沙替尼在印度的CML治疗中是有效的。成本限制了第二代酪氨酸激酶抑制剂在印度的使用。我们的观察结果不适合进行生存分析,但达沙替尼在疾病进展方面的作用及其耐受性需要得到认可。