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首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >CHOD/BVAM chemotherapy and whole-brain radiotherapy for newly diagnosed primary central nervous system lymphoma.
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CHOD/BVAM chemotherapy and whole-brain radiotherapy for newly diagnosed primary central nervous system lymphoma.

机译:新近诊断的原发性中枢神经系统淋巴瘤的CHOD / BVAM化疗和全脑放疗。

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PURPOSE: To assess the efficacy and toxicity of chemotherapy consisting of cyclophosphamide, doxorubicin (Adriamycin), vincristine, and dexamethasone (CHOD) plus bis-chloronitrosourea (BCNU), cytosine arabinoside, and methotrexate (BVAM) followed by whole-brain irradiation (WBRT) for patients with primary central nervous system lymphoma (PCNSL). METHODS AND MATERIALS: Patients 70 years old and younger with newly diagnosed, biopsy-proven PCNSL received one cycle of CHOD followed by two cycles of BVAM. Patients then received WBRT, 30.6 Gy, if a complete response was evoked, or 50.4 Gy if the response was less than complete; both doses were given in 1.8-Gy daily fractions. The primary efficacy endpoint was 1-year survival. RESULTS: Thirty-six patients (19 men, 17 women) enrolled between 1995 and 2000. Median age was 60.5 years (range, 34 to 69 years). Thirty (83%) patients had baseline Eastern Cooperative Oncology Group performance scores of 0 to 1. All 36 patients were eligible for survival and response evaluations. Median time to progression was 12.3 months, and median survival was 18.5 months. The percentages of patients alive at 1, 2, and 3 years were 64%, 36%, and 33%, respectively. The best response was complete response in 10 patients and immediate progression in 7 patients. Ten (28%) patients had at least one grade 3 or higher neurologic toxicity. CONCLUSIONS: This regimen did improve the survival of PCNSL patients but also caused substantial toxicity. The improvement in survival is less than that reported with high-dose methotrexate-based therapies.
机译:目的:评估由环磷酰胺,阿霉素(阿霉素),长春新碱和地塞米松(CHOD)加双氯亚硝基脲(BCNU),阿糖胞苷和甲氨蝶呤(BVAM)继之以全脑照射(WBRT)组成的化疗的疗效和毒性)适用于原发性中枢神经系统淋巴瘤(PCNSL)的患者。方法和材料:70岁及以下的新诊断,经活检证实的PCNSL患者和年轻患者接受1个周期的CHOD治疗,然后接受2个周期的BVAM治疗。然后,如果诱发完全缓解,则患者接受WBRT,30.6 Gy,如果缓解程度不完全,则接受50.4 Gy。两种剂量均以每天1.8Gy的剂量给药。主要功效终点为1年生存期。结果:1995年至2000年间共纳入36例患者(男19例,女17例)。中位年龄为60.5岁(范围34至69岁)。 30名(83%)患者的东部合作肿瘤小组基线表现评分为0到1。所有36例患者均符合生存和反应评估标准。进展的中位时间为12.3个月,中位生存期为18.5个月。存活1、2和3年的患者百分比分别为64%,36%和33%。最佳反应为10例患者完全缓解,7例患者立即进展。十名(28%)患者具有至少一种3级或更高的神经系统毒性。结论:该方案确实提高了PCNSL患者的生存率,但也引起了明显的毒性。存活率的改善少于以甲氨蝶呤为基础的大剂量疗法的报道。

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