Transplantation and Cell Therapy Unit, Department of Hematology, Institute Paoli-Calmettes, Marseille, France.
Exp Hematol. 2011 Sep;39(9):892-6. doi: 10.1016/j.exphem.2011.06.006. Epub 2011 Jun 16.
Rituximab is one of the most commonly used drugs in the treatment of B-cell non-Hodgkin lymphoma. Because of its ability to target CD20(+) lymphocytes, its use before allogeneic stem cell transplantation seemed to reduce risk of graft-vs.-host disease (GVHD) occurrence. We retrospectively analyzed the outcomes of adult patients diagnosed with CD20(+) lymphoproliferative disease undergoing allogeneic stem cell transplantation and receiving, or not receiving, rituximab up to 3 months before transplantation. Analysis on a cohort of 57 patients showed a protective role of rituximab on the occurrence of acute GVHD for those receiving anti-thymocyte globulin during conditioning (n = 39). Grade 2 to 4 and 3 to 4 acute GVHD occurred in 10% vs. 48% (p = 0.03) and 0% vs. 24% (p = 0.08) in the rituximab and no-rituximab groups, respectively. No impact on chronic GVHD was observed. These results confirm a protective role of rituximab on the occurrence of GVHD and enhance further investigation on future studies aimed at reducing GVHD incidence.
利妥昔单抗是治疗 B 细胞非霍奇金淋巴瘤最常用的药物之一。由于其能够靶向 CD20(+)淋巴细胞,因此在进行异基因干细胞移植前使用似乎可以降低移植物抗宿主病(GVHD)发生的风险。我们回顾性分析了接受异基因干细胞移植并在移植前 3 个月内接受或未接受利妥昔单抗治疗的 CD20(+)淋巴增殖性疾病的成年患者的结局。对 57 例患者的队列分析显示,对于接受预处理时使用抗胸腺细胞球蛋白的患者,利妥昔单抗具有降低急性 GVHD 发生的作用(n = 39)。利妥昔单抗组和未用利妥昔单抗组的 2 至 4 级和 3 至 4 级急性 GVHD 发生率分别为 10%和 48%(p = 0.03)和 0%和 24%(p = 0.08)。慢性 GVHD 无影响。这些结果证实了利妥昔单抗对 GVHD 发生的保护作用,并进一步增强了对未来旨在降低 GVHD 发生率的研究的探索。