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Therapy-related myelodysplastic syndrome/acute leukemia after multiple myeloma in the era of novel agents

机译:新药时代下与治疗相关的骨髓增生异常综合症/多发性骨髓瘤后的急性白血病

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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.
机译:多发性骨髓瘤患者的生存期增加了。美法仑和来那度胺均与随后的骨髓增生异常发展有关。我们回顾了三个中心在12年期间内发生了骨髓增生异常综合症(MDS)或急性非淋巴细胞性白血病(ANLL)随后发展的所有多发性骨髓瘤患者的病例。在确定的55名患者中,有2名在骨髓增生异常发生前仅接受来那度胺治疗。诊断多发性骨髓瘤与MDS / ANLL之间的中位时间为52.7个月。诊断为MDS或ANLL后的中位生存期为6.7个月。 MDS的治疗包括8例同种异体干细胞移植(中位生存期219天; 1例存活624天)和21例患者使用低甲基化药物(5例患者反应稳定或好转)。骨髓增生异常仍然是多发性骨髓瘤治疗的毁灭性并发症,生存期短,对可用方式的反应率差。

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