Badros Ashraf, Morris Christopher, Zangari Maurizio, Barlogie Bart, Tricot Guido
Myeloma and Transplantation Research Center, University of Arkansas for Medical Sciences, Little Rock, USA.
Leuk Lymphoma. 2002 Jun;43(6):1267-71. doi: 10.1080/10428190290026321.
We present five cases of concomitant relapsed multiple myeloma and therapy related myelodysplasia (t-MDS). After treatment with thalidomide marked anti-myeloma activity was observed, but it was associated with rapid progression of the MDS clone to acute myeloid leukemia (AML). This paradoxical effect of thalidomide is concerning because there is increasing use of thalidomide in relapsed, heavily treated multiple myeloma patients who already have a higher propensity to develop MDS. The leukemic transformation in our cases most probably reflects the natural progression of MDS, though it clearly demonstrates that thalidomide is ineffective in controlling blast proliferation in t-MDS. More concerning, however, is the possibility that thalidomide, while suppressing the myeloma clone, eliminates inhibitory signals and subsequently stimulates the proliferation of the leukemic clone. The use of thalidomide should be carefully assessed in relapsed multiple myeloma patients with clinical and cytogenetic evidence of t-MDS.
我们报告了5例复发性多发性骨髓瘤合并治疗相关骨髓增生异常综合征(t-MDS)的病例。使用沙利度胺治疗后,观察到明显的抗骨髓瘤活性,但它与MDS克隆迅速进展为急性髓系白血病(AML)相关。沙利度胺的这种矛盾效应令人担忧,因为在复发的、接受过大量治疗的多发性骨髓瘤患者中,沙利度胺的使用越来越多,而这些患者本身发生MDS的倾向就更高。我们病例中的白血病转化很可能反映了MDS的自然进展,不过这清楚地表明沙利度胺在控制t-MDS中的原始细胞增殖方面无效。然而,更令人担忧的是,沙利度胺在抑制骨髓瘤克隆的同时,可能消除了抑制信号,随后刺激了白血病克隆的增殖。对于有t-MDS临床和细胞遗传学证据的复发性多发性骨髓瘤患者,应仔细评估沙利度胺的使用。