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首页> 外文期刊>The West Indian medical journal. >Five-year follow-up of patients treated with imatinib mesylate for chronic myeloid leukaemia in Trinidad and Tobago.
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Five-year follow-up of patients treated with imatinib mesylate for chronic myeloid leukaemia in Trinidad and Tobago.

机译:特立尼达和多巴哥接受甲磺酸伊马替尼治疗的慢性粒细胞白血病患者的五年随访。

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摘要

OBJECTIVE: Data on the use of Imatinib (IM) in developing countries remain limited. A retrospective study was done to assess the efficacy and toxicity of IM in treating chronic myeloid leukaemia (CML) in Trinidad and Tobago. METHODS: Patients in all phases of CML who started IM therapy between February 2001 and February 2004 were included. All had received other previous therapy. They were assessed for haematological, cytogenetic and molecular response, overall survival (OS), event free survival (EFS) and adverse effects (AE). RESULTS: Twenty-five patients were followed-up for a median 61 months. At initiation of IM, 18 were in the chronic phase (CP), 3 in accelerated phase (AP), 3 in blast crisis (BC) and one in myelofibrotic transformation (MF). Overall, 96% of patients achieved complete haematological remission (CHR). Among CP patients, 67% attained a major cytogenetic response (MCR) and 44% a complete cytogenetic response (CCR). Overall survival and event free survival in the CP group were 82% and 76% respectively. Overall survival for advanced phase patients was 14% at 61 months. The adverse effects of IM were the same as previously described and generally tolerable. No patient opted to discontinue IM because of side effects. CONCLUSION: After 5 years of follow-up, IM was found to induce favourable and durable survival responses with an acceptable side effect profile in CP-CML patients who had received prior treatment with alternative agents.
机译:目的:关于发展中国家使用伊马替尼(IM)的数据仍然有限。进行了一项回顾性研究,以评估IM在特立尼达和多巴哥治疗慢性粒细胞白血病(CML)的功效和毒性。方法:纳入2001年2月至2004年2月开始IM治疗的CML所有阶段的患者。所有人都曾经接受过其他治疗。对他们的血液学,细胞遗传学和分子反应,总生存期(OS),无事件生存期(EFS)和不良反应(AE)进行了评估。结果:25例患者接受了中位61个月的随访。 IM开始时,有18个处于慢性期(CP),3个处于加速期(AP),3个处于爆炸性危机(BC)和1个处于骨髓纤维化转化(MF)。总体而言,有96%的患者达到了完全血液学缓解(CHR)。在CP患者中,有67%达到了主要的细胞遗传学应答(MCR),有44%达到了完整的细胞遗传学应答(CCR)。 CP组的总生存率和无事件生存率分别为82%和76%。晚期患者在61个月时的总生存率为14%。 IM的不利影响与先前描述的相同并且通常是可以忍受的。没有患者因为副作用而选择停止IM。结论:经过5年的随访,发现IM在接受过替代药物治疗的CP-CML患者中诱导了良好且持久的生存反应,并具有可接受的副作用。

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