Service d'Hématologie, Institut Universitaire du Cancer de Toulouse Oncopole, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.
Université Toulouse III Paul Sabatier, Toulouse, France.
Eur J Haematol. 2020 Sep;105(3):302-307. doi: 10.1111/ejh.13438. Epub 2020 May 25.
Complete responses have been observed in NPM1-mutated AML patients with dactinomycin, a nucleolar stress-inducing drug. Here, we report a single-center experience of compassionate use of dactinomycin in untreated or relapsed/ refractory NPM1-mutated AML.
From September 2015 to February 2019, 26 adult patients with NPM1-mutated AML received dactinomycin in different situations: front-line treatment in 4 unfit patients (16%); morphologic (n = 16, 62%), molecular relapses (n = 4, 16%), refractory disease (n = 1, 13%), or postremission therapy in second complete response (n = 1, 13%).
Median age was 62.5 years. Median number of dactinomycin cycle was 1 (1-8), and 7 patients (27%) received more than 3 cycles. Three out of 17 patients (18%) in morphologic relapse or refractory to chemotherapy achieved complete remission after the first cycle of dactinomycin. None of the 4 patients unfit for intensive chemotherapy responded to dactinomycin as front-line therapy. Grade 3-4 adverse events were thrombocytopenia (n = 11, 42%), neutropenia (n = 11, 42%), GI toxicity (n = 6, 23%), mucositis (n = 5, 19%), lung infection (n = 5, 19%), and skin rash (n = 2, 7.6%).
Dactinomycin is an inexpensive and easily available drug that may induce significant responses in few AML patients with NPM1 mutations with an acceptable safety profile.
在 NPM1 突变的急性髓系白血病(AML)患者中,观察到放线菌素 D(一种诱导核仁应激的药物)的完全缓解。在此,我们报告了在未经治疗或复发/难治性 NPM1 突变的 AML 患者中使用放线菌素 D 的单中心经验。
从 2015 年 9 月至 2019 年 2 月,26 例 NPM1 突变的 AML 成年患者在不同情况下接受了放线菌素 D 治疗:4 例不适合强化化疗的患者(16%)作为一线治疗;形态学复发(n=16,62%)、分子复发(n=4,16%)、难治性疾病(n=1,13%)或第二次完全缓解后的缓解后治疗(n=1,13%)。
中位年龄为 62.5 岁。中位放线菌素 D 周期数为 1(1-8),7 例患者(27%)接受了超过 3 个周期的治疗。17 例形态学复发或对化疗耐药的患者中,有 3 例(18%)在接受放线菌素 D 治疗的第 1 个周期后达到完全缓解。4 例不适合强化化疗的患者作为一线治疗,均未对放线菌素 D 产生反应。3-4 级不良事件包括血小板减少症(n=11,42%)、中性粒细胞减少症(n=11,42%)、胃肠道毒性(n=6,23%)、黏膜炎(n=5,19%)、肺部感染(n=5,19%)和皮疹(n=2,7.6%)。
放线菌素 D 是一种廉价且易于获得的药物,可能在少数具有 NPM1 突变的 AML 患者中诱导显著缓解,安全性可接受。