Subari Salih, Baidoun Firas, Hreh Muhanad, Patnaik Mrinal, Hashmi Shahrukh, Elliott Michelle, Hogan William, Litzow Mark, Al-Kali Aref
Division of Hematology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.
Int J Hematol. 2016 Apr;103(4):409-15. doi: 10.1007/s12185-016-1935-0. Epub 2016 Jan 18.
Patients with secondary acute myeloid leukemia (sAML) arising from prior myelodysplastic syndromes have poor prognosis. Anthracycline plus cytarabine (7 + 3) is a standard treatment option for patients who are fit for intensive therapy. In the present study, 22 of 96 sAML patients (23 %) were treated with 7 + 3 and achieved median overall survival (OS) of 9.8 months. Hypomethylating agents (HMA) were given for MDS in 6/22 (28 %) of the patients. When evaluating the prior HMA group, CR/CRi was 50 % for those with prior HMA exposure and 63 % for those without HMA exposure (P = 0.6). Median OS was 14 months for prior HMA exposure vs 10 months for no prior HMA (P = 0.9). The outcome of sAML patients who were treated with 7 + 3 continues to be poor. No statistical significant difference was found between response rates and mOS between prior HMA exposure or not. Additional larger studies are needed to confirm our results.
由先前的骨髓增生异常综合征引发的继发性急性髓系白血病(sAML)患者预后较差。蒽环类药物联合阿糖胞苷(7 + 3)是适合强化治疗患者的标准治疗方案。在本研究中,96例sAML患者中有22例(23%)接受了7 + 3治疗,中位总生存期(OS)为9.8个月。6/22(28%)的患者因骨髓增生异常综合征接受了去甲基化药物(HMA)治疗。在评估先前使用HMA的组时,先前暴露于HMA的患者CR/CRi为50%,未暴露于HMA的患者为63%(P = 0.6)。先前暴露于HMA的患者中位OS为14个月,未暴露于HMA的患者为10个月(P = 0.9)。接受7 + 3治疗的sAML患者的结局仍然较差。先前是否暴露于HMA之间的缓解率和中位总生存期未发现统计学显著差异。需要更多更大规模的研究来证实我们的结果。