Service d'Hématologie Clinique, CHU Amiens, France.
Am J Hematol. 2013 Jul;88(7):601-5. doi: 10.1002/ajh.23464. Epub 2013 May 30.
Despite progress in the understanding of leukemia pathophysiology, the treatment of acute myeloid leukemia (AML) remains challenging. In patients with refractory or relapsed (R/R) AML, the prognosis is still poor and this group is targeted for new drug development. We reviewed the outcome of 47 patients, with R/R AML after at least one course of intensive chemotherapy, treated with 5-azacytidine in three different French institutions. The overall response rate was 38% including complete remission in 21%, partial remission in 11%, and hematological improvement in 6% of cases. Median time to relapse was 6 (range, 1-39) months. Median overall survival was 9 months (not reached by responders vs. 4.5 months for nonresponders patients, P = 0.0001). Univariate analysis identified the absence of peripheral blood blasts and <20% bone marrow blasts as prognostic factors for both overall response and survival, but not age, ECOG/PS, type of AML, cytogenetic, status of the disease, number of previous lines of therapy, previous hematological stem cell transplantation, or white blood cells count. Bone marrow blasts percentage <20% was the only independent prognostic factor identified by multivariate analysis for overall response (P = 0.0013) and survival (P = 0.0324). Six patients in remission could proceed to an allogenic hematological stem cell transplantation. The drug-related grade 3/4 adverse events were hematopoietic toxicities (38%) and infection (32%). In conclusion, this study suggests that a salvage therapy with 5-azacytidine is an interesting option for patients with R/R AML after intensive chemotherapy. Prospective randomized studies are needed to demonstrate a superiority of this approach over others strategies.
尽管在白血病发病机制的理解方面取得了进展,但急性髓系白血病(AML)的治疗仍然具有挑战性。在难治性或复发性(R/R)AML 患者中,预后仍然较差,这一组是新药物开发的目标。我们回顾了在三个不同的法国机构中,至少接受过一次强化化疗的 47 例 R/R AML 患者接受 5-氮杂胞苷治疗的结果。总缓解率为 38%,包括完全缓解率 21%、部分缓解率 11%和血液学改善率 6%。中位复发时间为 6 个月(范围 1-39 个月)。中位总生存期为 9 个月(缓解者未达到,无缓解者为 4.5 个月,P=0.0001)。单因素分析确定外周血原始细胞和骨髓原始细胞<20%是总反应和生存的预后因素,但年龄、ECOG/PS、AML 类型、细胞遗传学、疾病状态、治疗线数、以前的造血干细胞移植或白细胞计数不是。骨髓原始细胞<20%是多因素分析中唯一确定的总反应(P=0.0013)和生存(P=0.0324)的独立预后因素。6 例缓解患者可进行同种异体造血干细胞移植。与药物相关的 3/4 级不良事件为血液学毒性(38%)和感染(32%)。总之,这项研究表明,强化化疗后 R/R AML 的补救性 5-氮杂胞苷治疗是一种很有前途的选择。需要进行前瞻性随机研究,以证明这种方法优于其他策略。