Castaño-Díez Sandra, López-Guerra Mónica, Bosch-Castañeda Cristina, Bataller Alex, Charry Paola, Esteban Daniel, Guijarro Francesca, Jiménez-Vicente Carlos, Castillo-Girón Carlos, Cortes Albert, Martínez-Roca Alexandra, Triguero Ana, Álamo José Ramón, Beà Silvia, Costa Dolors, Colomer Dolors, Rozman María, Esteve Jordi, Díaz-Beyá Marina
Hematology and Hematopathology Departments, Hospital Clínic Barcelona, 08036 Barcelona, Spain.
Medical School, University of Barcelona, 08036 Barcelona, Spain.
Cancers (Basel). 2022 Aug 25;14(17):4107. doi: 10.3390/cancers14174107.
Despite emerging molecular information on chronic myelomonocytic leukemia (CMML), patient outcome remains unsatisfactory and little is known about the transformation to acute myeloid leukemia (AML). In a single-center cohort of 219 CMML patients, we explored the potential correlation between clinical features, gene mutations, and treatment regimens with overall survival (OS) and clonal evolution into AML. The most commonly detected mutations were , , , and . Median OS was 34 months and varied according to age, cytogenetic risk, FAB, CPSS and CPSS-Mol categories, and number of gene mutations. Hypomethylating agents were administered to 37 patients, 18 of whom responded. Allogeneic stem cell transplantation (alloSCT) was performed in 22 patients. Two-year OS after alloSCT was 60.6%. Six patients received targeted therapy with or inhibitors, three of whom attained a long-lasting response. AML transformation occurred in 53 patients and the analysis of paired samples showed changes in gene mutation status. Our real-world data emphasize that the outcome of CMML patients is still unsatisfactory and alloSCT remains the only potentially curative treatment. However, targeted therapies show promise in patients with specific gene mutations. Complete molecular characterization can help to improve risk stratification, understand transformation, and personalize therapy.
尽管慢性粒单核细胞白血病(CMML)有了新出现的分子信息,但患者的预后仍然不尽人意,对于其向急性髓系白血病(AML)转化的了解也很少。在一个包含219例CMML患者的单中心队列中,我们探讨了临床特征、基因突变和治疗方案与总生存期(OS)以及向AML克隆进化之间的潜在相关性。最常检测到的突变是 、 、 和 。中位总生存期为34个月,并且根据年龄、细胞遗传学风险、FAB、CPSS和CPSS-Mol类别以及基因突变数量而有所不同。37例患者接受了去甲基化药物治疗,其中18例有反应。22例患者接受了异基因干细胞移植(alloSCT)。alloSCT后的两年总生存率为60.6%。6例患者接受了 或 抑制剂的靶向治疗,其中3例获得了持久反应。53例患者发生了AML转化,对配对样本的分析显示基因突变状态发生了变化。我们的真实世界数据强调,CMML患者的预后仍然不令人满意,alloSCT仍然是唯一可能治愈的治疗方法。然而,靶向治疗在具有特定基因突变的患者中显示出前景。完整的分子特征分析有助于改善风险分层、理解转化过程并实现个性化治疗。