Hematology, Department of Translational and Precision Medicine, Sapienza University, Via Benevento 6, 00161, Rome, Italy.
Department of Statistical Sciences, Sapienza University, Rome, Italy.
Ann Hematol. 2019 Aug;98(8):1891-1904. doi: 10.1007/s00277-019-03706-x. Epub 2019 May 11.
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.
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。