Service d'Hématologie Clinique, Hôpital Avicenne, Assistance Publique-Hôpitaux de Paris, Paris 13 University, France.
Haematologica. 2012 Feb;97(2):213-8. doi: 10.3324/haematol.2011.045914. Epub 2011 Oct 11.
Although lenalidomide is very effective in the treatment of anemia of lower risk myelodysplastic syndromes with 5q deletion (del 5q), concerns have been raised over the fact that this drug could trigger progression to acute myeloid leukemia in some patients.
Ninety-five transfusion-dependent patients with lower risk myelodysplastic syndromes with del 5q were treated with lenalidomide (10 mg/day, for 3 weeks every 4 weeks); six (6.3%) of the patients progressed to acute myeloid leukemia. This cohort of 95 lenalidomide-treated patients was compared to a historical control cohort of 99 patients with lower risk myelodysplastic syndromes with del 5q who never received lenalidomide, using a propensity score approach that can control for potential confounders in non-randomized comparisons.
The 4-year estimated cumulative incidence of leukemia was 9% in patients treated with lenalidomide and 15.8% in controls who did not receive lenalidomide (P=0.16).
Using a propensity score approach, we found no significant difference in acute myeloid leukemia progression and survival from diagnosis between the cohort treated with lenalidomide and the control cohort.
虽然来那度胺在治疗伴有 5q 缺失的低危骨髓增生异常综合征所致贫血方面非常有效,但人们担心该药物可能会导致一些患者进展为急性髓系白血病。
95 例依赖输血的伴有 5q 缺失的低危骨髓增生异常综合征患者接受来那度胺(每天 10mg,每 4 周的 3 周内用药)治疗;其中 6 例(6.3%)患者进展为急性髓系白血病。采用倾向评分方法,将这 95 例接受来那度胺治疗的患者与 99 例从未接受来那度胺治疗的伴有 5q 缺失的低危骨髓增生异常综合征患者进行比较,该方法可控制非随机比较中的潜在混杂因素。
接受来那度胺治疗的患者 4 年累积白血病发生率为 9%,未接受来那度胺治疗的对照组为 15.8%(P=0.16)。
使用倾向评分方法,我们发现接受来那度胺治疗的队列与对照组在急性髓系白血病进展和从诊断起的生存方面无显著差异。