Hematology, Department of Translational and Precision Medicine, Policlinico Umberto 1, Sapienza University, Rome, Italy.
Hematology, Department of Medical Sciences and Public Health, Businco Hospital ARNAS Brotzu, University of Cagliari, Cagliari, Italy.
Ann Hematol. 2021 May;100(5):1213-1219. doi: 10.1007/s00277-021-04477-0. Epub 2021 Mar 7.
Tyrosine kinase inhibitors (TKIs), the backbone of treatment for chronic phase chronic myeloid leukemia patients (CP-CML), have changed the long-term outcome of the disease. Nonetheless, over 20% of patients fail front-line therapy due to intolerance or resistance. A head-to-head comparison of dasatinib and nilotinib as second-line treatment outside of sponsored clinical trials has not been reported. We retrospectively analyzed 131 CP-CML patients who, after front-line imatinib failure, switched to a second-line therapy with nilotinib (59, 45%) or dasatinib (72, 55%). Median duration of second-line treatment was 33 months (range 2-100). The reason for switching therapy was resistance in 83.2% and intolerance in 16.8% of patients. The overall survival of the entire cohort at 7 years was 78.9%, while it was 72% and 85.6% for patients treated with dasatinib and nilotinib, respectively (p=0.287). With regard to efficacy after 12 months of treatment, 108 patients were evaluable for molecular response: 47% achieved a major molecular response and 18.2% a deep molecular response with dasatinib, compared to 38% and 16.2% with nilotinib (p=ns). We observed 35% of grade 3-4 adverse events, more frequently in the dasatinib group (47%) compared to the nilotinib group (22%), without affecting molecular responses. Our study suggests that, in the real-life setting, dasatinib and nilotinib used as second-line treatment in CP-CML are equally effective, with high molecular response rates and an acceptable tolerability.
酪氨酸激酶抑制剂(TKI)是慢性期慢性髓性白血病(CP-CML)患者治疗的基础,改变了疾病的长期预后。然而,超过 20%的患者因不耐受或耐药而在前一线治疗中失败。在赞助的临床试验之外,没有报道过达沙替尼和尼洛替尼作为二线治疗的头对头比较。我们回顾性分析了 131 例 CP-CML 患者,这些患者在前一线伊马替尼治疗失败后,改用尼洛替尼(59 例,45%)或达沙替尼(72 例,55%)作为二线治疗。二线治疗的中位持续时间为 33 个月(范围 2-100)。治疗转换的原因是 83.2%的患者耐药和 16.8%的患者不耐受。整个队列的 7 年总生存率为 78.9%,而达沙替尼和尼洛替尼治疗的患者分别为 72%和 85.6%(p=0.287)。关于治疗 12 个月后的疗效,108 例患者可评估分子反应:达沙替尼组有 47%的患者达到主要分子反应,18.2%的患者达到深度分子反应,而尼洛替尼组分别为 38%和 16.2%(p=ns)。我们观察到 35%的患者发生 3-4 级不良事件,达沙替尼组(47%)比尼洛替尼组(22%)更为常见,但不影响分子反应。我们的研究表明,在真实环境中,达沙替尼和尼洛替尼作为 CP-CML 的二线治疗同样有效,具有较高的分子反应率和可接受的耐受性。