Milpied N, Ifrah N, Kuentz M, Maraninchi D, Colombat P, Blaise D, Harousseau J L
Hôtel-Dieu, Nantes, France.
Br J Haematol. 1989 Sep;73(1):82-7. doi: 10.1111/j.1365-2141.1989.tb00224.x.
Twenty-five adult patients, 19 males, six females, age 16-43 years (median 23), with lymphoblastic lymphoma received allogeneic or autologous bone marrow transplantation in first complete remission. Twelve patients were Murphy stage IV with bone marrow and/or CNS involvement and 13 were stage III of whom nine had thoracic involvement. Complete remission was achieved with an intensive anthracycline containing multiagent chemotherapy protocol. Twelve patients with an HLA identical sibling received an allogeneic marrow and 13 without a donor received their own marrow harvested a median of 2 months (0-4 months) after complete remission and purged in vitro with either mafosfamide (eight patients) or anti T-cell monoclonal antibodies and complement (three patients). Bone marrow transplantation was performed 1-7 months (median 3 months) after achieving first complete remission. The conditioning regimen consisted of cyclophosphamide or high dose melphalan and total body irradiation. The actuarial 4-year disease-free survival is 68% (+/- 9% SE). The actuarial probability of relapse was 26% (+/- 3% SE) with a median follow up to 22 months. There was no difference between allogeneic and autologous transplantation with eight out of 12 allo patients in first continuous complete remission 26-45 months after transplant and nine out of 13 auto in continuous complete remission 15-75 months after transplant. These results compare favourably with those achieved with the best chemotherapeutic regimen used for such patients.
25例成年淋巴细胞性淋巴瘤患者(19例男性,6例女性,年龄16 - 43岁,中位年龄23岁)在首次完全缓解期接受了异基因或自体骨髓移植。12例患者为墨菲IV期,有骨髓和/或中枢神经系统受累,13例为III期,其中9例有胸部受累。通过含蒽环类药物的强化多药化疗方案实现了完全缓解。12例有HLA相同同胞的患者接受了异基因骨髓移植,13例无供者的患者接受了自体骨髓移植,自体骨髓在完全缓解后中位2个月(0 - 4个月)采集,并在体外使用马磷酰胺(8例患者)或抗T细胞单克隆抗体及补体(3例患者)进行净化处理。在首次完全缓解后1 - 7个月(中位3个月)进行骨髓移植。预处理方案包括环磷酰胺或大剂量美法仑及全身照射。4年无病生存率的精算值为68%(±9%标准误)。复发的精算概率为26%(±3%标准误),中位随访时间为22个月。异基因移植和自体移植之间无差异,12例异基因移植患者中有8例在移植后26 - 45个月处于首次持续完全缓解期,13例自体移植患者中有9例在移植后15 - 75个月处于持续完全缓解期。这些结果与使用最佳化疗方案治疗此类患者所取得的结果相比更具优势。