Abrey L E, Yahalom J, DeAngelis L M
Departments of Neurology and Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
J Clin Oncol. 2000 Sep;18(17):3144-50. doi: 10.1200/JCO.2000.18.17.3144.
The use of preradiotherapy (RT) methotrexate (MTX) has improved disease control and survival in patients with primary CNS lymphoma (PCNSL). The reported protocol was designed to optimize and enhance the chemotherapeutic component of treatment.
Fifty-two patients were treated with five cycles of high-dose MTX 3.5 g/m(2), procarbazine 100 mg/m(2)/d, and vincristine 1.4 mg/m(2). Thirty patients received whole-brain RT (45 Gy). Twenty-two older patients deferred RT to diminish the risk of delayed neurotoxicity; these patients are compared with 12 older patients who completed the entire treatment regimen. Most patients (n = 35) received high-dose cytarabine after RT.
Objective response rate to the induction chemotherapy regimen was 90%; overall median survival is 60 months. Grade 3 or 4 myelosuppression was seen in 30 patients, primarily in association with cytarabine; grade 3 nephrotoxicity due to MTX was seen in two patients. Older patients had similar median survival with or without the addition of RT: 32 versus 33 months, respectively. However, late neurotoxicity was significantly more common in those older patients who received RT (P: =.00004). Patients younger than 60 years who received the complete treatment regimen have not reached median disease-free or overall survival.
Increasing the dose of MTX and adding procarbazine and vincristine improved disease control and overall survival in patients with newly diagnosed PCNSL. Younger patients in particular fared extremely well with this treatment regimen. In older patients, deferring whole-brain RT did not compromise overall survival but did reduce treatment-related toxicity.
放疗前使用甲氨蝶呤(MTX)可改善原发性中枢神经系统淋巴瘤(PCNSL)患者的疾病控制情况并提高生存率。所报道的方案旨在优化和强化治疗中的化疗部分。
52例患者接受了5个周期的高剂量MTX(3.5 g/m²)、丙卡巴肼(100 mg/m²/天)和长春新碱(1.4 mg/m²)治疗。30例患者接受了全脑放疗(45 Gy)。22例老年患者推迟放疗以降低迟发性神经毒性风险;将这些患者与12例完成整个治疗方案的老年患者进行比较。大多数患者(n = 35)在放疗后接受了高剂量阿糖胞苷治疗。
诱导化疗方案的客观缓解率为90%;总体中位生存期为60个月。30例患者出现3级或4级骨髓抑制,主要与阿糖胞苷有关;2例患者出现因MTX导致的3级肾毒性。老年患者无论是否接受放疗,中位生存期相似:分别为32个月和33个月。然而,接受放疗的老年患者中迟发性神经毒性明显更常见(P = 0.00004)。接受完整治疗方案的60岁以下患者尚未达到无病生存期或总生存期的中位数。
增加MTX剂量并添加丙卡巴肼和长春新碱可改善新诊断PCNSL患者的疾病控制和总生存期。特别是年轻患者采用该治疗方案效果极佳。对于老年患者,推迟全脑放疗不会影响总生存期,但确实降低了治疗相关毒性。