Gertz Morie A, Terpos Evangelos, Dispenzieri Angela, Kumar Shaji, Shah Rupin A, Orlowski Robert, Kastritis Efstathios, Dimopoulos Meletios A, Shah Jatin
Division of Hematology.
Leuk Lymphoma. 2015 Jun;56(6):1723-6. doi: 10.3109/10428194.2014.970543. Epub 2014 Nov 3.
Survival for patients with multiple myeloma has increased. Both melphalan and lenalidomide are associated with subsequent development of myelodysplasia. We reviewed the cases of all patients with multiple myeloma who had subsequent development of myelodysplastic syndrome (MDS) or acute non-lymphoblastic leukemia (ANLL) during a 12-year period in three centers. Of 55 patients identified, two received only lenalidomide before myelodysplasia developed. The median time between the diagnoses of multiple myeloma and MDS/ANLL was 52.7 months. Median survival after the diagnosis of MDS or ANLL was 6.7 months. Treatment of MDS comprised allogeneic stem cell transplant in eight patients (median survival, 219 days; one patient alive at 624 days) and a hypomethylating agent in 21 patients (response of stable or better in five patients). Myelodysplasia remains a devastating complication of therapy for multiple myeloma, with short survival and poor response rates to available modalities.
多发性骨髓瘤患者的生存率有所提高。美法仑和来那度胺都与随后发生的骨髓发育异常有关。我们回顾了三个中心在12年期间所有随后发生骨髓增生异常综合征(MDS)或急性非淋巴细胞白血病(ANLL)的多发性骨髓瘤患者的病例。在确诊的55例患者中,有2例在发生骨髓发育异常之前仅接受过来那度胺治疗。多发性骨髓瘤诊断与MDS/ANLL诊断之间的中位时间为52.7个月。MDS或ANLL诊断后的中位生存期为6.7个月。MDS的治疗包括8例患者接受异基因干细胞移植(中位生存期219天;1例患者在624天时仍存活)和21例患者接受低甲基化药物治疗(5例患者病情稳定或好转)。骨髓发育异常仍然是多发性骨髓瘤治疗的一种毁灭性并发症,生存率低且对现有治疗方式的反应率差。