Wu Jing-Jing, Wang Xin-Hua, Li Ling, Li Xin, Zhang Lei, Sun Zhen-Chang, Fu Xiao-Rui, Ma Wang, Chang Yu, Zhang Xu-Dong, Han Li-Juan, Zhang Ming-Zhi
Institute of Clinical Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan Province, China E-mail :
Asian Pac J Cancer Prev. 2014;15(11):4733-8. doi: 10.7314/apjcp.2014.15.11.4733.
We developed and evaluated a regimen including fotemustine, teniposide and dexamethasone (FTD) for treating patients with central nervous system (CNS) lymphoma based on pharmacokinetic properties of individual agents and in combination.
In a comparison study, 8 patients with primary CNS lymphoma (PCNSL) and 8 with secondary CNS lymphoma (SCNSL) were treated with FTD (comprising fotemustine 100 mg/m2, 1h infusion, day 1; teniposide 60 mg/m2, >0.5 h infusion, on day 2, 3, 4; dexamethasone 40 mg, 1h infusion, on day 1, 2, 3, 4 and 5; and methotrexate 12 mg, cytosine arabinoside 50 mg plus dexamethasone 5 mg intrathecally, on day 2 and 7). Cycles were repeated every 3 weeks. After response assessment, patients received whole brain radiotherapy.
Of the 8 PCNSL patients, 4 (50%) achieved CR and 3 (38%) PR, an overall response rate of 88%. Four patients (50%) were in continuing remission at the end of this study after a median follow-up of 30 months (range 10 to 56 months). Of the 8 SCNSL patients the overall response rate was 63% (CR+PR:38%+25%). All responses were achievable with predictable toxicity mainly reflecting reversible myelosuppression.
This study suggests that FTD could be an effective treatment for CNS lymphoma, and is worthy of further evaluation.
基于各药物的药代动力学特性及联合用药情况,我们研发并评估了一种包含福莫司汀、替尼泊苷和地塞米松(FTD)的方案用于治疗中枢神经系统(CNS)淋巴瘤患者。
在一项对照研究中,8例原发性CNS淋巴瘤(PCNSL)患者和8例继发性CNS淋巴瘤(SCNSL)患者接受了FTD治疗(包括福莫司汀100mg/m²,第1天静脉输注1小时;替尼泊苷60mg/m²,第2、3、4天静脉输注超过0.5小时;地塞米松40mg,第1、2、3、4和5天静脉输注1小时;甲氨蝶呤12mg、阿糖胞苷50mg加地塞米松5mg鞘内注射,第2天和第7天)。每3周重复一个周期。在疗效评估后,患者接受全脑放疗。
8例PCNSL患者中,4例(50%)达到完全缓解(CR),3例(38%)达到部分缓解(PR),总缓解率为88%。在本研究结束时,经过中位30个月(范围10至56个月)的随访,4例患者(50%)持续缓解。8例SCNSL患者的总缓解率为63%(CR + PR:分别为38% + 25%)。所有缓解均可实现,且毒性可预测,主要表现为可逆性骨髓抑制。
本研究表明FTD可能是CNS淋巴瘤的一种有效治疗方法,值得进一步评估。