Han S, Wang M, Liu B, Yu J
The Department of Oncology, Shandong Cancer Hospital and Institute, Shandong University, No. 440 of Jiyan Road, Jinan, 250117, Shandong, People's Republic of China.
The Department of Oncology, Jiaozhou Central Hospital of Qingdao, No. 29 of Xuzhou Road, Jiaozhou, Qingdao, 266300, Shandong, People's Republic of China.
Clin Transl Oncol. 2016 Feb;18(2):138-43. doi: 10.1007/s12094-015-1345-4. Epub 2015 Jul 14.
The aim of this study was to evaluate the efficacy and safety of a consecutive series of elderly patients with primary central nervous system lymphoma (PCNSL) treated with single-agent pemetrexed without radiotherapy or intrathecal chemotherapy.
Twelve histologically confirmed newly diagnosed PCNSL patients older than 65 years were studied between 2008 and 2013. An induction chemotherapy was initially given (pemetrexed 600 mg/m(2) on day 1, every 3 weeks). Patients achieving a complete, partial response or stable disease proceeded to a maintenance phase (up to 6 cycles). Patients with progressive/recurrent disease (PD) were treated with whole brain radiotherapy on an individual basis.
Four patients presented complete response, six patients showed partial response and two patients presented progressive disease. The median progression-free survival (PFS) was 9.0 months [95 % confidence interval (CI) 2.0-45.3] and the median overall survival was 19.5 months (95 % CI 5.0-45.3). Adverse events included leukocytopenia, anemia, fatigue, rash and vomiting. No neurotoxicity or treatment-related death was observed. The estimated 1-year and 2-year survival rate was 66.7 and 41.7 %, respectively.
Our efficacy results demonstrate that the single-agent pemetrexed was feasible, active and well tolerated in elderly patients with PCNSL. Furthermore, this single-agent regimen results in higher response rates and less toxicity comparable with other chemotherapy or radiotherapy regimens. Prospectively, controlled studies are warranted to confirm such results.
本研究旨在评估连续一系列老年原发性中枢神经系统淋巴瘤(PCNSL)患者接受单药培美曲塞治疗(不联合放疗或鞘内化疗)的疗效和安全性。
2008年至2013年期间对12例经组织学确诊的65岁以上新诊断PCNSL患者进行了研究。最初给予诱导化疗(第1天静脉滴注培美曲塞600mg/m²,每3周一次)。达到完全缓解、部分缓解或疾病稳定的患者进入维持治疗阶段(最多6个周期)。疾病进展/复发(PD)的患者根据个体情况接受全脑放疗。
4例患者达到完全缓解,6例患者部分缓解,2例患者疾病进展。中位无进展生存期(PFS)为9.0个月[95%置信区间(CI)2.0 - 45.3],中位总生存期为19.5个月(95%CI 5.0 - 45.3)。不良事件包括白细胞减少、贫血、疲劳、皮疹和呕吐。未观察到神经毒性或治疗相关死亡。估计1年和2年生存率分别为66.7%和41.7%。
我们的疗效结果表明,单药培美曲塞对老年PCNSL患者是可行、有效的,且耐受性良好。此外,与其他化疗或放疗方案相比,这种单药方案导致更高的缓解率和更低的毒性。前瞻性对照研究有必要证实这些结果。