Schwenn M R, Blattner S R, Lynch E, Weinstein H J
Division of Pediatric Hematology/Oncology, Boston Floating Hospital, MA.
J Clin Oncol. 1991 Jan;9(1):133-8. doi: 10.1200/JCO.1991.9.1.133.
We designed a protocol that included 2 months of intensive Cytoxan (cyclophosphamide; Bristol-Myers Co, Evansville, IN), high-dose methotrexate (MTX), high-dose cytarabine (ara-C), and vincristine (HiC-COM) to improve event-free survival (EFS) for patients with advanced-stage Burkitt's lymphoma and B-cell acute lymphoblastic leukemia (ALL). We also wished to test the feasibility of rapidly cycling Cytoxan and high-dose ara-C based on signs of early marrow recovery. Twenty patients including 12 with stage III Burkitt's lymphoma and eight with stage IV Burkitt's lymphoma or B-cell ALL were entered onto this pilot study. The rate of complete remission was 95%. Four patients have relapsed. The 2-year actuarial EFS was 75% (median follow-up, 37 months). Two of the initial five patients developed transverse myelitis, which we believe may have been secondary to the concomitant administration of intrathecal (IT) and high-dose systemic ara-C. We conclude that this short but intensive regimen is highly effective for patients with advanced Burkitt's lymphoma and B-cell ALL. EFS has improved over previous less intensive regimens, and is comparable to regimens of longer duration.
我们设计了一种方案,其中包括为期2个月的密集环磷酰胺(Cytoxan;百时美公司,印第安纳州埃文斯维尔)、大剂量甲氨蝶呤(MTX)、大剂量阿糖胞苷(ara-C)和长春新碱(HiC-COM),以提高晚期伯基特淋巴瘤和B细胞急性淋巴细胞白血病(ALL)患者的无事件生存期(EFS)。我们还希望根据早期骨髓恢复的迹象来测试快速循环使用环磷酰胺和大剂量阿糖胞苷的可行性。20名患者进入了这项初步研究,其中包括12例III期伯基特淋巴瘤患者和8例IV期伯基特淋巴瘤或B细胞ALL患者。完全缓解率为95%。4名患者复发。2年精算EFS为75%(中位随访时间为37个月)。最初的5名患者中有2名发生了横贯性脊髓炎,我们认为这可能是鞘内注射(IT)和大剂量全身性阿糖胞苷联合使用的继发结果。我们得出结论,这种短疗程但高强度的方案对晚期伯基特淋巴瘤和B细胞ALL患者非常有效。EFS比以前强度较低的方案有所改善,并且与疗程较长的方案相当。