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丙卡巴肼、洛莫司汀与长春新碱或替莫唑胺:哪种方案更佳?

Procarbazine, lomustine and vincristine or temozolomide: which is the better regimen?

作者信息

Lassman Andrew B

机构信息

Department of Neurology & Herbert Irving Comprehensive, Cancer Center, Columbia University Medical Center, 710 West 168th Street, NY, USA.

出版信息

CNS Oncol. 2015;4(5):341-6. doi: 10.2217/cns.15.36. Epub 2015 Nov 6.

Abstract

Anaplastic oligodendrogliomas (AOs) are rare brain tumors responsive to chemotherapy with procarbazine, lomustine (CCNU) and vincristine (PCV), especially when harboring 1p19q codeletion. However, with the emergence of temozolomide as an easier to administer and less toxic alternative regimen, PCV fell out of favor. Now, long-term results of two Phase III studies conceived in the 1990s, Radiation Therapy Oncology Group (RTOG) 9402 and European Organisation for Research and Treatment of Cancer (EORTC) 26951, resurrected debate about the potential role of PCV. No adequately powered prospective trial has compared chemotherapy alone with PCV versus temozolomide for newly diagnosed 1p19q codeleted AOs. Available data suggest responses may be both more frequent and more durable with PCV, and survival may be longer. Which regimen is 'better', therefore, depends on the importance of different metrics (i.e., toxicity, complexity, efficacy), and await definitive results from the important ongoing and recently redesigned CODEL international Phase III trial.

摘要

间变性少突胶质细胞瘤(AO)是一种罕见的脑肿瘤,对丙卡巴肼、洛莫司汀(CCNU)和长春新碱(PCV)联合化疗有反应,尤其是当存在1p19q共缺失时。然而,随着替莫唑胺作为一种更易于给药且毒性较小的替代方案出现,PCV不再受青睐。现在,两项于20世纪90年代开展的III期研究——放射治疗肿瘤学组(RTOG)9402和欧洲癌症研究与治疗组织(EORTC)26951——的长期结果,重新引发了关于PCV潜在作用的争论。对于新诊断的1p19q共缺失的AO,尚无足够样本量的前瞻性试验比较单纯化疗与PCV及替莫唑胺的疗效。现有数据表明,PCV的反应可能更频繁、更持久,生存期可能更长。因此,哪种方案“更好”取决于不同指标(即毒性、复杂性、疗效)的重要性,有待正在进行且最近重新设计的CODEL国际III期试验的最终结果。

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