Department of Hematology and Medical Oncology, Al Bairouni University Hospital, Damascus University, Damascus, Syria,
Med Oncol. 2013 Dec;30(4):690. doi: 10.1007/s12032-013-0690-9. Epub 2013 Aug 20.
Treatment of primary central nervous system lymphoma (PCNSL) associates with low response rates and poor survival using conventional radio and chemotherapy. Due to its favorable toxicity profile, temozolomide has emerged as a new option for treatment of PCNSL in young patients. In this study, we report a series of PCNSL patients treated with an innovative regimen combining high dose of both cytarabine and methotrexate with temozolomide without radiotherapy or intrathecal chemotherapy. To evaluate a new intensive chemotherapy with temozolomide, trying to assess response and progression-free survival rates and if the results are promising, we are aiming at evaluating the overall survival (OS) taking into consideration the toxicity profile. The study was performed at Al Mowassa Charity Hospital in Damascus (Syria). Forty patients with histologically confirmed PCNSL median age 52 years (range 20-65) years were included. Biopsies were cultured, and a karyotyping was made in 32 patients. An induction chemotherapy was started, and methotrexate 3 gr/m² over 12 h on day 1, cytarabine 3 gr/m² every 12 h on day 1 and temozolomide 150 mg/m² from day 2 through day 6 with a total of 6 cycles were given on a monthly basis. Among the 40 patients included in the study, a complete response was observed in 34 patients (85%) and a partial response in the remaining 6 patients (15%). Disease progressed in 8 out of 40 patients (20%) while 32 patients are still living at 5 years making the OS reaching 77%. Grade II nephrotoxicity was observed in 2 patients while grade III and IV hematotoxicity was observed in 5 patients. High dose of both Ara-C and MTX combined with temozolomide appears to be a good choice in the treatment of PCNSL, in the light of good response and OS rates, taking into consideration the acceptable toxicity profile. However, a larger trial is needed to make it an acceptable new combination as a first line for PCNSL patients.
原发性中枢神经系统淋巴瘤 (PCNSL) 的治疗采用常规放化疗,反应率低,生存率差。替莫唑胺由于其良好的毒性特征,已成为年轻 PCNSL 患者治疗的新选择。在本研究中,我们报告了一系列采用联合大剂量阿糖胞苷和甲氨蝶呤联合替莫唑胺治疗的 PCNSL 患者,未进行放疗或鞘内化疗。为了评估替莫唑胺新的强化化疗方案,尝试评估反应率和无进展生存率,并且如果结果有希望,我们旨在考虑毒性特征来评估总生存率(OS)。该研究在叙利亚大马士革的 Al Mowassa 慈善医院进行。40 名经组织学证实的 PCNSL 患者入组,中位年龄 52 岁(范围 20-65 岁)。对活检标本进行培养,并对 32 名患者进行核型分析。开始诱导化疗,甲氨蝶呤 3g/m²,持续 12 小时,第 1 天;阿糖胞苷 3g/m²,每 12 小时 1 次,第 1 天;替莫唑胺 150mg/m²,第 2-6 天,每月 1 个周期,共 6 个周期。在入组的 40 例患者中,34 例(85%)患者达到完全缓解,6 例(15%)患者达到部分缓解。40 例患者中有 8 例(20%)疾病进展,32 例患者仍存活 5 年,总生存率(OS)达到 77%。2 例患者出现 2 级肾毒性,5 例患者出现 3-4 级血液学毒性。大剂量阿糖胞苷和甲氨蝶呤联合替莫唑胺治疗 PCNSL 反应率和 OS 率良好,考虑到可接受的毒性特征,似乎是一种不错的选择。然而,需要更大的试验来使其成为 PCNSL 患者一线治疗的可接受的新联合方案。