首页> 外文期刊>Bone marrow transplantation >High-dose chemotherapy with autologous stem cell transplantation as first-line therapy for primary CNS lymphoma in patients younger than 60 years: a multicenter phase II study of the GOELAMS group.
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High-dose chemotherapy with autologous stem cell transplantation as first-line therapy for primary CNS lymphoma in patients younger than 60 years: a multicenter phase II study of the GOELAMS group.

机译:大剂量化疗加自体干细胞移植作为60岁以下患者原发性中枢神经系统淋巴瘤的一线治疗:GOELAMS组的多中心II期研究。

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摘要

The optimum treatment of primary CNS lymphoma (PCNSL) is not yet determined. The objective of this study was to assess the safety and efficacy of initial methotrexate-based chemotherapy followed by high-dose chemotherapy (HDT) with autologous stem cell transplantation (ASCT) in patients with newly diagnosed PCNSL. Twenty-five patients received two courses of initial chemotherapy combining methotrexate, etoposide, carmustine and methylprednisolone, and one course of ifosfamide-cytarabine followed by peripheral stem cell collection. Seventeen responsive patients then received HDT using carmustine, etoposide, cytarabine and melphalan with autologous stem cell rescue. After ASCT for responding patients or after salvage therapy for non-responders, whole brain radiation therapy at a dose of 30 Gy was delivered. The objective response rate to the induction chemotherapy was 84%. Four of the 21 responding patients did not have ASCT because of toxicity or refusal. With a median follow-up time of 34 months, the projected event free survival rate is 46% at 4 years. Projected overall survival is 64% at 4 years. Sixteen patients are actually in continuous complete response. No evidence of late treatment-related toxicity was observed. This treatment approach appears feasible in newly diagnosed PCNSL with encouraging results.
机译:尚未确定原发性CNS淋巴瘤(PCNSL)的最佳治疗方法。这项研究的目的是评估在初次诊断为PCNSL的患者中,以甲氨蝶呤为基础的初始化疗,然后进行大剂量化疗(HDT)和自体干细胞移植(ASCT)的安全性和有效性。 25例患者接受了两个疗程的初始化疗,联合甲氨蝶呤,依托泊苷,卡莫司汀和甲基泼尼松龙,以及一个疗程的异环磷酰胺-阿糖胞苷,然后收集外周干细胞。然后用卡莫司汀,依托泊苷,阿糖胞苷和美法仑通过自体干细胞抢救对17名反应性患者进行HDT。在对有反应的患者进行ASCT治疗后或对无反应的患者进行挽救治疗后,进行了3​​0 Gy剂量的全脑放射治疗。诱导化疗的客观缓解率为84%。 21名有反应的患者中有4名因毒性反应或拒绝而没有ASCT。平均随访时间为34个月,预计4年无事件生存率是46%。预计4年总生存率为64%。实际上有16名患者处于持续的完全缓解状态。没有观察到后期治疗相关毒性的证据。这种治疗方法在新诊断的PCNSL中似乎可行,并且结果令人鼓舞。

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