首页> 外文期刊>Neurology India. >Phase II trial of temozolomide plus concurrent whole-brain radiation followed by TNV regimen as adjuvant therapy for patients with newly diagnosed primary CNS lymphoma
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Phase II trial of temozolomide plus concurrent whole-brain radiation followed by TNV regimen as adjuvant therapy for patients with newly diagnosed primary CNS lymphoma

机译:替莫唑胺联合同期全脑放疗联合TNV方案作为初诊中枢神经系统淋巴瘤患者的辅助治疗的II期试验

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Background: Primary central nervous system lymphoma (PCNSL) is an aggressive extranodal non-Hodgkin′s lymphoma limited to the CNS. Treatment of PCNSL with high-dose methotrexate (HD-MTX)-based chemotherapy and whole-brain radiotherapy (WBRT) is associated with high rates of relapse and severe treatment-related neurotoxicity. Aim: To report our experience of treating newly diagnosed PCNSL with temozolomide, nedaplatin, and vincristine (TNV), as the replacement of HD-MTX, in combination with concurrent chemoradiotherapy. Materials and Methods: Newly diagnosed PCNSL patients were given concurrent temozolomide (75 mg/m 2 , orally) daily during WBRT. Then, the TNV regimen was given after four weeks. The TNV regimen consisted of temozolomide (200 mg/m 2 orally: Days 1-5), nedaplatin (80 mg/m 2 intravenous: Day 1), and vincristine (1.4 mg/m 2 intravenous: Day 1). Each cycle was of a duration of four weeks and a maximum of six cycles were applied. The primary end point was response to treatment obtained by magnetic resonance imaging (MRI). Secondary end points were progression-free survival (PFS) and fewer toxic effects. Results: The study subjects included 14 patients (median age: 53.5, median Karnofsky Performance Scale (KPS): 75). The median number of TNV cycles given was five. Response to treatment: Complete response in 12 (85.7%) patients, partial response in 2 (14.3%) patients, and none with progressive disease. The objective response rate was 100%, and median PFS was 21.4 months. Toxicity was relatively mild, which mainly included nausea in six and fatigue in five, grade 3-4 hematotoxicity in one, and abnormal liver functions in five patients. No neurotoxicity has been observed till date. Conclusion: The efficacy outcomes in this study are comparable to other reported HD-MTX-based regimens plus WBRT, with an added favorable toxicity profile. Prospective, randomized controlled trials are warranted to confirm such results.
机译:背景:原发性中枢神经系统淋巴瘤(PCNSL)是一种侵袭性结外非霍奇金淋巴瘤,仅限于中枢神经系统。基于高剂量甲氨蝶呤(HD-MTX)的化学疗法和全脑放射疗法(WBRT)的PCNSL治疗与复发率高和严重的治疗相关的神经毒性有关。目的:报告我们使用替莫唑胺,奈达铂和长春新碱(TNV)替代HD-MTX并用同步放化疗治疗新诊断的PCNSL的经验。材料和方法:WBRT期间,每天向新诊断的PCNSL患者同时给予替莫唑胺(75 mg / m 2,口服)。然后,在四个星期后给予TNV方案。 TNV方案包括替莫唑胺(口服200 mg / m 2:第1-5天),奈达铂(80 mg / m 2静脉内:第1天)和长春新碱(1.4 mg / m 2静脉内:第1天)。每个周期为四个星期,最多可应用六个周期。主要终点是对通过磁共振成像(MRI)获得的治疗的反应。次要终点是无进展生存期(PFS)和较少的毒性作用。结果:研究对象包括14名患者(中位年龄:53.5,中位数卡诺夫斯基绩效量表(KPS):75)。给出的TNV周期的中位数为5。对治疗的反应:12例患者(85.7%)完全缓解,2例患者(14.3%)完全缓解,无进展性疾病。客观缓解率为100%,中位PFS为21.4个月。毒性相对较轻,主要包括六种恶心和五种疲劳,三分之一到三级血液毒性和五名肝功能异常。迄今为止尚未观察到神经毒性。结论:本研究的疗效结果与其他已报道的基于HD-MTX的方案加WBRT相当,并具有良好的毒性。保证进行前瞻性,随机对照试验以证实此类结果。

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