Kazda T, Lakomý R, Poprach A, Pospíšil P, Jančálek R, Šlampa P
Klin Onkol. 2017 Fall;30(5):337-342. doi: 10.14735/amko2017337.
The optimal treatment for low-grade gliomas remains controversial. Neurosurgery, radiotherapy, and chemotherapy are the main treatment options. Despite advances in oncology, there are still a lot of uncertainties, and the optimal sequences, combinations, and timings of these procedures have not yet been optimized. It is still unclear whether temozolomide can replace effective, but toxic PCV chemotherapy (procarbazine, lomustine, vincristine) and whether temozolomide can be used upfront alone instead of radiotherapy alone. Mature results from phase III trials (CODEL, EORTC 22033-26033) will provide answers to these questions. Correlative analyses of survival data and molecular marker findings (1p/19q codeletion, IDH1/2 mutation, and MGMT promoter methylation status) are essential. Due to slow progressive nature of the disease, all clinical trials with low-grade gliomas are complicated by the need for long-term follow-up to obtain valid mature data, which makes any new treatment procedures or developments in basic research developed during the course of closed clinical trials difficult to apply in daily clinical practice. An example is the recently published RTOG 9802 study evaluating the role of adjuvant PCV in combination with radiotherapy for the treatment of high-risk low-grade glioma patients where the recruitment of patients was initiated almost two decades ago. Health-related quality of life after treatment of patients with expected long-term survival is also very important and its maintenance is currently the focus of considerable interest.
The main objective of the present review is to summarize the results of key clinical trials and highlight controversial issues that could have an impact on future daily practice. Another aim is to discuss these issues in the light of newly established molecular markers from the new 2016 WHO Classification of Tumors of the Central Nervous System.Key words: glioma - astrocytoma - radiotherapy - temozolomide - PCV - cognition This work was supported by MH CZ - RVO (MMCI, 00209805) and by project of the Ministry of Education, Youths and Sports of the Czech Republic CEITEC 2020 (LQ1601). The authors declare they have no potential conflicts of interest concerning drugs, products, or services used in the study. The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers.Submitted: 21. 2. 2017Accepted: 20. 3. 2017.
低级别胶质瘤的最佳治疗方案仍存在争议。神经外科手术、放疗和化疗是主要的治疗选择。尽管肿瘤学领域取得了进展,但仍存在许多不确定性,这些治疗手段的最佳顺序、组合和时机尚未得到优化。替莫唑胺是否能取代有效但有毒的PCV化疗(丙卡巴肼、洛莫司汀、长春新碱),以及替莫唑胺是否可以单独作为初始治疗而非单纯放疗,目前仍不清楚。III期试验(CODEL、EORTC 22033 - 26033)的成熟结果将为这些问题提供答案。生存数据与分子标志物结果(1p/19q共缺失、IDH1/2突变和MGMT启动子甲基化状态)的相关性分析至关重要。由于该疾病进展缓慢,所有针对低级别胶质瘤的临床试验都因需要长期随访以获得有效的成熟数据而变得复杂,这使得在封闭临床试验过程中开展的任何新治疗手段或基础研究进展都难以应用于日常临床实践。一个例子是最近发表的RTOG 9802研究,该研究评估辅助PCV联合放疗在治疗高危低级别胶质瘤患者中的作用,其患者招募几乎始于二十年前。预期长期生存患者治疗后的健康相关生活质量也非常重要,目前维持其生活质量是备受关注的焦点。
本综述的主要目的是总结关键临床试验的结果,并突出可能影响未来日常实践的争议性问题。另一个目的是根据2016年新版《中枢神经系统肿瘤WHO分类》中新确立的分子标志物来讨论这些问题。
胶质瘤 - 星形细胞瘤 - 放疗 - 替莫唑胺 - PCV - 认知
本研究得到了捷克卫生部 - RVO(MMCI,00209805)以及捷克教育、青年和体育部CEITEC 2020项目(LQ1601)的支持。作者声明他们在研究中使用的药物、产品或服务方面不存在潜在利益冲突。编辑委员会声明该手稿符合ICMJE对生物医学论文的推荐标准。
2017年2月21日
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