酪氨酸激酶抑制剂(博苏替尼)对曾接受过治疗的慢性髓性白血病患者的治疗效果(伊拉克患者样本)

IF 0.1 Q4 HEMATOLOGY Iraqi Journal of Hematology Pub Date : 2024-05-16 DOI:10.4103/ijh.ijh_59_23
Anfal Mumtaz Ahmed, B. Matti
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引用次数: 0

摘要

慢性髓性白血病(CML)是一种骨髓增生性肿瘤,其特点是恶性髓细胞在骨髓和外周血中过度聚集。这种疾病主要由一种称为t(9;22) (q34.13;q11.23) 的特殊染色体易位引发,这种易位会导致 BCR-ABL 融合基因的形成。随着针对 BCR-ABL1 激酶活性的酪氨酸激酶抑制剂(TKIs)获得批准,CML 的治疗前景发生了重大变化。其中一种抑制剂是博舒替尼,该药已上市数年,用于治疗对以往疗法耐药或不耐受的慢性、加速和爆发期CML患者。 这项研究旨在评估博舒替尼作为CML患者二线疗法的疗效和安全性,以及坚持治疗对患者反应的影响。 这项前瞻性队列研究于 2021 年 10 月至 2022 年 10 月在巴格达医疗城综合体的血液学中心招募了 85 名 CML 患者。所有患者都至少使用了一种 TKI 治疗失败,并开始接受升级剂量的博舒替尼治疗。患者在3个月和6个月时接受随访,评估分子和细胞遗传学反应,并仔细监测不良事件(AEs)。博舒替尼的依从性也通过特定的依从性量表进行监测,以优化治疗反应率。 患者的平均年龄为(47.3 ± 14.9)岁(18-77 岁),男女比例为 1.4:1。CML患者的状态显示,89.4%处于慢性期,5.8%处于加速期,4.7%处于爆发期。关于博舒替尼之前使用过的 TKIs 数量,72.9% 的患者在使用过一种 TKIs(伊马替尼)后失败。根据2013年欧洲白血病网络标准,6个月时(72.3%),患者达到最佳应答。胃肠道症状和皮肤表现是博舒替尼最常见的非血液学不良反应。根据9项莫里斯基用药依从性量表(Morisky Medication Adherence Scale),42%的患者坚持用药,这与较高的最佳反应数有显著关联(P = 0.0001)。 博舒替尼作为CML患者的后续治疗药物,疗效显著,应答率高,前景广阔。坚持用药对博舒替尼的最佳疗效起着重要作用。
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Treatment outcome of the tyrosine kinase inhibitor (bosutinib) in previously treated chronic myeloid leukemia patients (sample of Iraqi patients)
Chronic myeloid leukemia (CML) is a type of myeloproliferative neoplasm characterized by the excessive accumulation of malignant myeloid cells in the bone marrow and peripheral blood. This condition is primarily triggered by a specific chromosomal translocation known as t(9;22) (q34.13;q11.23), which leads to the formation of the BCR-ABL fusion gene. The treatment landscape for CML has undergone significant changes with the approval of tyrosine kinase inhibitors (TKIs) targeting the BCR-ABL1 kinase activity. One such inhibitor is bosutinib, which has been available for several years to treat patients with chronic, accelerated, and blast-phase CML who have shown resistance or intolerance to previous therapies. The aim of this study was to assess efficacy and safety of Bosutinib as a 2nd line therapy in CML patients, in addition to effect of adherence to treatment on patients response. Eighty-five patients with CML were enrolled in a prospective cohort study from October 2021 to October 2022 at Hematology Center in Medical City Complex – Baghdad. All patients failed to at least one TKI, and all of them started escalated dose of bosutinib. The patients were followed-up by assessing molecular and cytogenetic response at 3 and 6 months and monitored carefully for adverse events (AEs) which were graded by common terminology IX criteria for AEs version 5. Adherence to bosutinib was also monitored by a specific adherence scale to optimize the response rate to treatment. The mean age of patients was 47.3 ± 14.9 (range: 18–77), with male:female ratio 1.4:1. Status of CML patients showed that 89.4% were in the chronic phase, 5.8% in accelerated phase, and 4.7% in blast phase. Regarding the number of previous TKIs before bosutinib, 72.9% of patients failed to prior one TKI (imatinib). At 6 months (72.3%), patients achieve optimal response according to European Leukemia Net criteria 2013. Gastrointestinal symptoms and dermatological manifestations were the most common nonhematological AEs of bosutinib. According to 9-item Morisky Medication Adherence Scale, 42% of patients were adherent to medication which showed a significant association with a higher number of optimal response (P = 0.0001). Bosutinib is effective with a high and promising response as a subsequent line treatment in CML patients, and it is generally safe and associated with mild-to-moderate tolerable and manageable AEs. Adherence to the drug plays a significant role in optimal response to bosutinib.
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