First Department of Internal Medicine.
Blood. 2014 Mar 13;123(11):1658-64. doi: 10.1182/blood-2013-07-512657. Epub 2014 Jan 29.
Therapy-related acute myeloid leukemia and myelodysplastic syndromes (t-AML/MDS) represent severe late effects in patients treated for Hodgkin lymphoma (HL). Because more recent data are scarce, we retrospectively analyzed incidence, outcome, and risk factors for the development of t-AML/MDS after HL. A total of 11,952 patients treated for newly diagnosed HL within German Hodgkin Study Group trials between 1993 and 2009 were considered. At a median follow-up of 72 months, t-AML/MDS was diagnosed in 106/11,952 patients (0.9%). Median time from HL treatment to t-AML/MDS was 31 months. The median age of patients with t-AML/MDS was higher than in the whole patient group (43 vs 34 years, P < .0001). Patients who received 4 or more cycles of BEACOPP(escalated) had an increased risk to develop t-AML/MDS when compared with patients treated with less than 4 cycles of BEACOPP(escalated) or no BEACOPP chemotherapy (1.7% vs 0.7% vs 0.3%, P < .0001). The median overall survival (OS) for all t-AML/MDS patients was 7.2 months. However, t-AML/MDS patients proceeding to allogeneic stem cell transplantation had a significantly better outcome with a median OS not reached after a median follow-up of 41 months (P < .001).
治疗相关性急性髓系白血病和骨髓增生异常综合征(t-AML/MDS)是接受霍奇金淋巴瘤(HL)治疗的患者发生的严重晚期效应。由于最近的数据较少,我们回顾性分析了 HL 治疗后 t-AML/MDS 的发生率、结局和危险因素。共考虑了 1993 年至 2009 年期间德国霍奇金研究组试验中治疗新诊断的 HL 的 11952 例患者。中位随访 72 个月时,11952 例患者中有 106 例(0.9%)诊断为 t-AML/MDS。从 HL 治疗到 t-AML/MDS 的中位时间为 31 个月。t-AML/MDS 患者的中位年龄高于整个患者组(43 岁 vs 34 岁,P <.0001)。与接受少于 4 个周期 BEACOPP(递增)治疗或未接受 BEACOPP 化疗的患者相比,接受 4 个或更多周期 BEACOPP(递增)治疗的患者发生 t-AML/MDS 的风险增加(1.7% vs 0.7% vs 0.3%,P <.0001)。所有 t-AML/MDS 患者的中位总生存期(OS)为 7.2 个月。然而,接受异基因造血干细胞移植的 t-AML/MDS 患者的结局显著改善,中位随访 41 个月后中位 OS 未达到(P <.001)。