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真实世界中接受伊马替尼治疗的慢性期慢性髓性白血病患者的 10 年结局。

Ten-year outcome of chronic-phase chronic myeloid leukemia patients treated with imatinib in real life.

机构信息

Hematology, Department of Translational and Precision Medicine, Sapienza University, Via Benevento 6, 00161, Rome, Italy.

Department of Statistical Sciences, Sapienza University, Rome, Italy.

出版信息

Ann Hematol. 2019 Aug;98(8):1891-1904. doi: 10.1007/s00277-019-03706-x. Epub 2019 May 11.

Abstract

Imatinib, the first BCR/ABL kinase inhibitor approved for the treatment of chronic myeloid leukemia (CML), has changed the long-term outcome of patients affected by this disease. The aim of our analysis was to report, after a median follow-up of 10.2 years (range 5.8-14.8), the long-term outcome, efficacy, and safety of imatinib treatment (frontline and after interferon failure) in a single institution cohort of 459 patients with CML in chronic phase treated outside of clinical trials. The 10-year overall survival of the whole cohort was 77.1%, while the 10-year probability of dying due to CML and other causes was 7.8% and 16%, respectively. The prognostic value of the BCR-ABL1 ratio at 3 months (⩽ 10%) and of complete cytogenetic response and major molecular response at 1 year was confirmed also in the real-life practice. The EUTOS long-term survival score better stratified the baseline risk of dying of CML compared with other risk scores. Two hundred thirty-six (51.4%) patients achieved a deep molecular response during imatinib treatment after a median time of 4.57 years, and 95 (20.6%) had a stable deep molecular response maintained for at least 2 consecutive years. Imatinib was associated with a low rate of serious cardiovascular events and second neoplasia. This 10-year real-life follow-up study shows that imatinib maintains efficacy over time and that long-term administration of imatinib is not associated with notable cumulative or late toxic effects.

摘要

伊马替尼是第一个被批准用于治疗慢性髓性白血病 (CML) 的 BCR/ABL 激酶抑制剂,改变了患有这种疾病的患者的长期预后。我们分析的目的是在一项单中心队列研究中报告,经过中位随访 10.2 年(范围 5.8-14.8 年)后,伊马替尼(一线和干扰素失败后)治疗在慢性期 CML 459 例患者中的长期疗效、安全性和疗效,这些患者未参与临床试验。整个队列的 10 年总生存率为 77.1%,而 10 年因 CML 和其他原因死亡的概率分别为 7.8%和 16%。在实际治疗中,也证实了 3 个月时 BCR-ABL1 比值(⩽10%)和 1 年时完全细胞遗传学缓解和主要分子缓解的预后价值。EUTOS 长期生存评分与其他风险评分相比,更好地分层了 CML 死亡的基线风险。236 名(51.4%)患者在伊马替尼治疗中位时间 4.57 年后达到深度分子缓解,95 名(20.6%)患者至少连续 2 年保持稳定的深度分子缓解。伊马替尼与严重心血管事件和第二肿瘤的发生率低相关。这项为期 10 年的真实随访研究表明,伊马替尼随着时间的推移保持疗效,长期服用伊马替尼不会导致明显的累积或晚期毒性作用。

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