Department of Hematology and Immunology, Kanazawa Medical University, 1-1 Daigaku, Uchinada, Ishikawa, 920-0293, Japan.
Department of Pathology and Laboratory Medicine, Kanazawa Medical University, 1-1 Daigaku, Uchinada, Ishikawa, 920-0293, Japan.
Int J Hematol. 2011 Jun;93(6):720-726. doi: 10.1007/s12185-011-0848-1. Epub 2011 May 15.
We describe MR-CHOP therapy, a novel treatment regimen consisting of high-dose methotrexate and R-CHOP that provides systemic anti-tumor activity with penetration of the blood-brain barrier in patients with newly diagnosed primary central nervous system lymphoma. The MR-CHOP regimen was administered with 2 g/m(2) of methotrexate and 375 mg/m(2) of rituximab on day 1, 750 mg/m(2) of cyclophosphamide on day 3, 50 mg/m(2) of doxorubicin on day 3, 1.4 mg/m(2) of vincristine on day 3 and 100 mg of prednisolone on days 1-5 in this pilot study of seven patients. Six cycles of MR-CHOP therapy were administered every 3 weeks, followed by high-dose chemotherapy with stem cell rescue in young patients, or an additional two cycles of 4 g/m(2) methotrexate and rituximab in older patients. The overall response rate was 100%, with 85.7% complete remission (CR). One patient showed partial response, relapsed and subsequently died. Another relapsed following CR, and was rescued by further salvage therapy. The others survive without relapse at a median observation period of 24 months. Hematological toxicity included grade 4 leukocytopenia in 4/7 and neutropenia in 5/7, which were transient and tolerated well. Non-hematological toxicities were tolerated well. The efficacy of this novel regimen as remission induction therapy was found to be promising in this pilot study, although the number of patients was small and follow-up short.
我们描述了 MR-CHOP 治疗方案,这是一种新的治疗方案,由高剂量甲氨蝶呤和 R-CHOP 组成,为新诊断的原发性中枢神经系统淋巴瘤患者提供了全身抗肿瘤活性,并穿透血脑屏障。在这项 7 例患者的初步研究中,MR-CHOP 方案在第 1 天给予 2 g/m2 甲氨蝶呤和 375 mg/m2 利妥昔单抗,第 3 天给予 750 mg/m2 环磷酰胺,第 3 天给予 50 mg/m2 阿霉素,第 3 天给予 1.4 mg/m2 长春新碱,第 1-5 天给予 100 mg 泼尼松。每 3 周给予 6 个周期的 MR-CHOP 治疗,然后在年轻患者中进行大剂量化疗和干细胞挽救,或在老年患者中给予另外 2 个周期的 4 g/m2 甲氨蝶呤和利妥昔单抗。总缓解率为 100%,完全缓解率为 85.7%。1 例患者显示部分缓解,复发后死亡。另 1 例在 CR 后复发,经进一步挽救性治疗获救。其他患者在中位观察期 24 个月时无复发存活。血液学毒性包括 4/7 例患者出现 4 级白细胞减少和 5/7 例患者出现中性粒细胞减少,均为一过性,且耐受性良好。非血液学毒性可耐受。尽管患者数量较少,随访时间较短,但这项新方案作为缓解诱导治疗的疗效在这项初步研究中显示出了很大的希望。