Mohty M, Attal M, Marit G, Bulabois C E, Garban F, Gratecos N, Rio B, Vernant J P, Sotto J J, Cahn J Y, Blaise D, Jouet J P, Facon T, Yakoub-Agha I
Unité de Transplantation et de Thérapie Cellulaire (UTTC), Institut Paoli-Calmettes, Marseille, France.
Bone Marrow Transplant. 2005 Jan;35(2):165-9. doi: 10.1038/sj.bmt.1704756.
Thalidomide is effective in multiple myeloma (MM), even in patients who have relapsed after high-dose therapy. A potent graft-versus-myeloma (GVM) effect can be induced against MM after allogeneic stem cell transplantation (allo-SCT). In all, 31 MM patients received thalidomide as a salvage therapy after progression following allo-SCT. The median maximum daily dose of thalidomide was 200 mg (range, 50-600). Thalidomide had to be discontinued in six patients (19%) because of toxicity. In all, nine patients (29%; 95% CI, 13-45) achieved an objective response with thalidomide therapy (six partial and three very good partial responses, VGPR). Five patients developed graft-versus-host disease (GVHD) after thalidomide therapy, including the three patients achieving a VGPR. These data demonstrate that thalidomide is potentially effective in MM patients failing allo-SCT.
沙利度胺对多发性骨髓瘤(MM)有效,即使是在接受大剂量治疗后复发的患者中。异基因干细胞移植(allo-SCT)后可诱导产生强大的移植物抗骨髓瘤(GVM)效应来对抗MM。总共有31例MM患者在allo-SCT进展后接受沙利度胺作为挽救治疗。沙利度胺的最大日剂量中位数为200mg(范围为50-600mg)。6例患者(19%)因毒性不得不停用沙利度胺。总共有9例患者(29%;95%CI,13-45)在沙利度胺治疗后获得客观缓解(6例部分缓解和3例非常好的部分缓解,VGPR)。5例患者在沙利度胺治疗后发生移植物抗宿主病(GVHD),包括3例获得VGPR的患者。这些数据表明沙利度胺对allo-SCT失败的MM患者可能有效。