Division of Hematology/Oncology, Department of Medicine, University of Maryland School of Medicine and Marlene and Stewart Greenebaum Cancer Center, University of Maryland, Baltimore, MD, USA.
Haematologica. 2013 Apr;98(4):584-90. doi: 10.3324/haematol.2012.062547. Epub 2012 Nov 9.
Prior studies have investigated patients' characteristics, treatments, and outcomes for older adults with myelodysplastic syndromes, but most failed to distinguish chronic myelomonocytic leukemia. Recognizing potentially important differences between the diseases, we undertook a population-based comparison of baseline characteristics, treatments, and outcomes between older adults with chronic myelomonocytic leukemia and myelodysplastic syndromes. The patients' data were obtained from Surveillance Epidemiology and End Results registry data from 2001-2005, linked to Medicare claims. Baseline characteristics, treatment (red blood cell transfusions, hematopoietic growth factors, hypomethylating agents, chemotherapy or transplantation), progression to acute myeloid leukemia, and overall survival were compared using bivariate techniques. Multivariate logistic regression estimated differences in treatments received. Cox proportional hazard models estimated the effects of chronic myelomonocytic leukemia relative to myelodysplastic syndromes on progression-free survival. A larger proportion of patients with chronic myelomonocytic leukemia (n=792), compared to patients with myelodysplastic syndromes (n=7,385), failed to receive any treatment (25% versus 15%; P<0.0001), or only received red blood cell transfusions (19.8% versus 16.7%; P=0.037). A larger percentage of patients with chronic myelomonocytic leukemia progressed to acute myeloid leukemia (42.6% versus 15.5%, respectively; P<0.0001), with shorter time to progression. Chronic myelomonocytic leukemia patients had a shorter median survival (13.3 versus 23.3 months; P<0.0001) and lower 3-year survival rate (19% versus 36%; P<0.0001). Adjusted estimates, controlling for baseline characteristics and selected treatments, indicate that chronic myelomonocytic leukemia was associated with an increased risk of progression to acute myeloid leukemia or death (HR 2.22; P<0.0001), compared to myelodysplastic syndromes. In conclusion, chronic myelomonocytic leukemia is less frequently treated in older adults and is associated with worse outcomes, even after controlling for the patients' baseline characteristics and selected treatments. Our data suggest the need for continued evaluation of the biological differences between these diseases and clinical trials targeting chronic myelomonocytic leukemia.
先前的研究已经调查了老年骨髓增生异常综合征患者的特征、治疗和结局,但大多数研究未能区分慢性髓单核细胞白血病。为了认识到这些疾病之间可能存在的重要差异,我们对老年慢性髓单核细胞白血病和骨髓增生异常综合征患者的基线特征、治疗和结局进行了一项基于人群的比较。患者数据来自 2001 年至 2005 年的监测、流行病学和最终结果登记数据,并与医疗保险索赔数据相关联。使用双变量技术比较了基线特征、治疗(红细胞输注、造血生长因子、低甲基化剂、化疗或移植)、进展为急性髓细胞白血病和总生存情况。多变量逻辑回归估计了所接受治疗的差异。Cox 比例风险模型估计了慢性髓单核细胞白血病相对于骨髓增生异常综合征对无进展生存期的影响。与骨髓增生异常综合征患者(n=7,385)相比,更多的慢性髓单核细胞白血病患者(n=792)未接受任何治疗(25%对 15%;P<0.0001),或仅接受红细胞输注(19.8%对 16.7%;P=0.037)。更多的慢性髓单核细胞白血病患者进展为急性髓细胞白血病(分别为 42.6%和 15.5%;P<0.0001),且进展时间更短。慢性髓单核细胞白血病患者的中位生存期更短(13.3 对 23.3 个月;P<0.0001),3 年生存率更低(19%对 36%;P<0.0001)。调整后的估计值,在控制基线特征和选定的治疗后,表明与骨髓增生异常综合征相比,慢性髓单核细胞白血病与进展为急性髓细胞白血病或死亡的风险增加相关(HR 2.22;P<0.0001)。总之,即使在控制了患者的基线特征和选定的治疗后,老年慢性髓单核细胞白血病患者的治疗频率也较低,结局也较差。我们的数据表明,需要继续评估这些疾病之间的生物学差异,并开展针对慢性髓单核细胞白血病的临床试验。