Division of Hematology, Department of Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, Tokyo, Japan.
Am J Hematol. 2012 Sep;87(9):929-31. doi: 10.1002/ajh.23261. Epub 2012 Jun 5.
Although allogeneic hematopoietic stem cell transplantation (HSCT) is considered the only curative treatment for refractory or relapsed follicular lymphoma (FL), transplant-related mortality (TRM) greatly interferes with the success. A variety of reduced-intensity conditionings (RICs) have been used to reduce TRM, but an optimal conditioning for FL has not been fully established. We retrospectively evaluated the outcome of allogeneic HSCT for FL with RIC consisting of fludarabine and melphalan. Nineteen adult patients with relapsed or refractory FL were conditioned with fludarabine (125 mg/m2) and melphalan (140 mg/m2), and received grafts from an HLA-identical sibling (n = 6) or an unrelated donor (n = 13). For the prophylaxis of graft-versus-host disease (GVHD), cyclosporine A or tacrolimus with short-term methotrexate was given. There were no early deaths before engraftment, and all patients achieved engraftment. Three patients died of extensive-type chronic GVHD (n = 2) or bacterial infection (n = 1) without disease progression. With a median follow-up period of 75.2 months (range: 33.3–111.9 months), 16 patients were alive without disease progression. Both the 5-year overall and progression-free survival rates were 84.2% (95% CI: 67.7–100%). These results strongly suggest that allogeneic HSCT with RIC using fludarabine and melphalan could be a promising treatment choice for refractory or relapsed FL.
虽然异基因造血干细胞移植(HSCT)被认为是治疗难治性或复发性滤泡性淋巴瘤(FL)的唯一根治方法,但移植相关死亡率(TRM)极大地干扰了其成功。已经使用了各种减低强度的预处理方案(RIC)来降低 TRM,但尚未完全确定 FL 的最佳预处理方案。我们回顾性评估了 FL 患者接受包含氟达拉滨和马法兰的 RIC 的异基因 HSCT 的结果。19 例复发或难治性 FL 成人患者接受氟达拉滨(125mg/m2)和马法兰(140mg/m2)预处理,并接受 HLA 完全匹配的同胞供体(n=6)或无关供体(n=13)的移植物。为预防移植物抗宿主病(GVHD),给予环孢素 A 或他克莫司联合短期甲氨蝶呤。在植入前没有早期死亡,所有患者均植入成功。3 例患者死于广泛型慢性 GVHD(n=2)或细菌感染(n=1),无疾病进展。中位随访期为 75.2 个月(范围:33.3-111.9 个月),16 例患者无疾病进展且存活。5 年总生存率和无进展生存率均为 84.2%(95%CI:67.7-100%)。这些结果强烈表明,使用氟达拉滨和马法兰的 RIC 异基因 HSCT 可能是难治性或复发性 FL 的一种有前途的治疗选择。