Department of Medical Oncology, Austin Health, 145 Studley Road, Melbourne, Victoria 3084, Australia.
J Clin Neurosci. 2012 Nov;19(11):1501-5. doi: 10.1016/j.jocn.2012.04.001. Epub 2012 Sep 17.
Primary central nervous system lymphoma (PCNSL) is a rare form of extra-nodal non-Hodgkin lymphoma. Although recommendations for first-line treatment usually incorporate high-dose methotrexate, there is substantial heterogeneity in the types of salvage therapies used at relapse. Phase II data supported the use of temozolomide as a well-tolerated treatment modality in this setting. Therefore, we reviewed the treatment and outcomes of patients with relapsed PCNSL who were treated with salvage temozolomide at our institution. Seven patients were treated with salvage temozolomide between January 2000 and May 2011. The objective response rate was 14%. Progression-free survival was 2 months (95% confidence interval [CI]: 0-5.9) and median overall survival was 4 months (95% CI: 0-13). Toxicity was mild, with one episode of grade 3 neutropenia during 25 cycles of chemotherapy. Although these results are consistent with previous phase II results, the outcomes for these patients remain extremely poor. The low toxicity of temozolomide raises the possibility of combining temozolomide with other chemotherapeutic agents or targeted agents in future clinical trials.
原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见的结外非霍奇金淋巴瘤。虽然一线治疗的建议通常包括大剂量甲氨蝶呤,但在复发时使用的挽救治疗类型存在很大的异质性。II 期数据支持替莫唑胺作为该情况下耐受性良好的治疗方式。因此,我们回顾了在我们机构接受挽救性替莫唑胺治疗的复发性 PCNSL 患者的治疗和结果。2000 年 1 月至 2011 年 5 月期间,有 7 名患者接受了挽救性替莫唑胺治疗。客观缓解率为 14%。无进展生存期为 2 个月(95%置信区间[CI]:0-5.9),中位总生存期为 4 个月(95%CI:0-13)。毒性轻微,25 个化疗周期中有 1 例出现 3 级中性粒细胞减少症。尽管这些结果与之前的 II 期结果一致,但这些患者的预后仍然非常差。替莫唑胺的低毒性提出了在未来的临床试验中联合替莫唑胺与其他化疗药物或靶向药物的可能性。