Nagle Sarah J, Shah Nirav N, Ganetsky Alex, Landsburg Daniel J, Nasta Sunita D, Mato Anthony, Schuster Stephen J, Reshef Ran, Tsai Donald E, Svoboda Jakub
Lymphoma Program, Abramson Cancer Center, University of Pennsylvania, Perelman Center for Advanced Medicine, 3400 Civic Center Blvd, 2 West Pavilion, Philadelphia, PA 19104, USA.
Medical College of Wisconsin, 9200 W. Wisconsin Ave, Milwaukee, WI 53226, USA.
Int J Hematol Oncol. 2017 Dec;6(4):113-121. doi: 10.2217/ijh-2017-0020. Epub 2018 Jan 26.
To describe the long-term outcomes of patients with lymphoma in the CNS treated with rituximab, temozolomide and high-dose methotrexate without consolidation therapy.
PATIENTS & METHODS: A retrospective cohort study of 46 consecutive patients with primary CNS lymphoma (PCNSL, 27 patients) or secondary CNS involvement of diffuse large B-cell lymphoma (DLBCL, 19 patients) who were treated with rituximab on day 1 in combination with high-dose methotrexate (days 1 and 15) and temozolomide (days 1-5) in 28-day cycles without further consolidation.
Median follow-up was 21.2 months. Patients received a median of five cycles (range 1-15). Median overall survival (OS) was 26 months and median progression-free survival was 8.6 months. At 3 years, 37% of patients were alive and without evidence of disease. The patients with PCNSL had a significantly higher response rates (ORR 81 vs 47%; p = 0.015) and longer median OS (55.3 vs 4.8 months; p < 0.01) than those with secondary CNS DLBCL. Toxicities were mild and manageable.
The rituximab, temozolomide and methotrexate regimen is an effective therapy for patients with PCNSL without the toxicities typically associated with consolidation therapy.
描述接受利妥昔单抗、替莫唑胺和大剂量甲氨蝶呤治疗且未进行巩固治疗的中枢神经系统淋巴瘤患者的长期预后。
一项回顾性队列研究,纳入46例连续患者,其中原发性中枢神经系统淋巴瘤(PCNSL,27例)或弥漫性大B细胞淋巴瘤继发性中枢神经系统受累(DLBCL,19例),患者在第1天接受利妥昔单抗治疗,并联合大剂量甲氨蝶呤(第1天和第15天)和替莫唑胺(第1 - 5天),每28天为一个周期,不再进行进一步巩固治疗。
中位随访时间为21.2个月。患者接受的中位周期数为5个周期(范围1 - 15个周期)。中位总生存期(OS)为26个月,中位无进展生存期为8.6个月。3年时,37%的患者存活且无疾病证据。PCNSL患者的缓解率显著高于继发性中枢神经系统DLBCL患者(客观缓解率[ORR] 81%对47%;p = 0.015),中位OS更长(55.3个月对4.8个月;p < 0.01)。毒性反应轻微且可控。
利妥昔单抗、替莫唑胺和甲氨蝶呤方案是治疗PCNSL患者的有效疗法,且无通常与巩固治疗相关的毒性。