Pentsova Elena, Deangelis Lisa M, Omuro Antonio
Department of Neurology, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY, 10065, USA,
J Neurooncol. 2014 Mar;117(1):161-5. doi: 10.1007/s11060-014-1370-0. Epub 2014 Jan 31.
The prognosis of primary CNS lymphoma (PCNSL) recurring after methotrexate is poor (objective response rates [ORR] = 26-53 %; 1-year overall survival [OS] = 35-57 %). Salvage PCNSL chemotherapies have been based on the use of different agents to avoid cross-resistance; however, methotrexate is the most active agent in PCNSL, and methotrexate re-challenge may be an effective strategy for recurrent disease. We report our experience with methotrexate re-challenge in PCNSL. We reviewed 39 patients with histologically confirmed PCNSL who responded to methotrexate at initial diagnosis, experienced disease relapse and received methotrexate re-challenge. At the time of re-challenge, median age was 66 and median Karnofsky performance score (KPS) was 70. Median time from initial diagnosis was 26 m. Twenty-six patients were at first relapse and 13 at second or later relapse. At re-challenge, methotrexate was given in combination with other agents to 33 patients and as a single agent to six. The objective response rate was 85 %, with a complete response in 29 (75 %) patients, partial response in four (10 %) and disease progression in six (15 %). At median follow-up of 26 m, the median progression-free survival was 16 m; 1-year OS was 79 % (95 % CI 63-89) and median OS was 41 m. KPS was a prognostic factor for progression free survival (p = 0.04). In this population selected by previous methotrexate response, methotrexate re-challenge was a safe and effective strategy, indicating chemosensitivity was retained. Efficacy compared favorably to other salvage treatments suggesting methotrexate re-challenge should be considered in recurrent PCNSL patients who previously responded to methotrexate.
甲氨蝶呤治疗后复发的原发性中枢神经系统淋巴瘤(PCNSL)预后较差(客观缓解率[ORR]=26 - 53%;1年总生存率[OS]=35 - 57%)。挽救性PCNSL化疗一直基于使用不同药物以避免交叉耐药;然而,甲氨蝶呤是PCNSL中最有效的药物,再次使用甲氨蝶呤可能是复发性疾病的一种有效策略。我们报告了我们在PCNSL中再次使用甲氨蝶呤的经验。我们回顾了39例经组织学确诊的PCNSL患者,这些患者在初始诊断时对甲氨蝶呤有反应,经历疾病复发并接受了甲氨蝶呤再次治疗。再次治疗时,中位年龄为66岁,中位卡诺夫斯基性能评分(KPS)为70分。从初始诊断开始的中位时间为26个月。26例患者为首次复发,13例为第二次或更晚复发。再次治疗时,33例患者接受甲氨蝶呤与其他药物联合使用,6例患者接受甲氨蝶呤单药治疗。客观缓解率为85%,其中29例(75%)患者完全缓解,4例(10%)部分缓解,6例(15%)疾病进展。在中位随访26个月时,中位无进展生存期为16个月;1年总生存率为79%(95%CI 63 - 89),中位总生存期为41个月。KPS是无进展生存期的一个预后因素(p = 0.04)。在这个由先前甲氨蝶呤反应所选择的人群中,再次使用甲氨蝶呤是一种安全有效的策略,表明保留了化疗敏感性。与其他挽救性治疗相比,疗效良好,这表明对于先前对甲氨蝶呤有反应的复发性PCNSL患者应考虑再次使用甲氨蝶呤。