Suppr超能文献

单纯化疗作为少突胶质细胞瘤一线治疗的作用。

Role of exclusive chemotherapy as first line treatment in oligodendroglioma.

作者信息

Sunyach Marie Pierre, Jouvet Anne, Perol David, Jouanneau Emmanuel, Guyotat Jacques, Gignoux Laurence, Carrie Christian, Frappaz Didier

机构信息

Radiotherapy and Neuro-Oncology Unit, Centre Léon Bérard, Lyon, France.

出版信息

J Neurooncol. 2007 Dec;85(3):319-28. doi: 10.1007/s11060-007-9422-3. Epub 2007 Jun 14.

Abstract

PURPOSE

The optimal therapy of oligodendrogliomas remains uncertain. Although chemosensitive, these tumors are not chemocurable. We investigated whether chemotherapy delays the need for radiation therapy (RT) without decreasing length and quality of survival.

METHODS AND MATERIALS

Among 89 patients treated for oligodendrogliomas at the Centre Léon Bérard of Lyon from 1982 to 1999, 59 patients fitted inclusion criteria, having had centrally reviewed pure oligodendroglioma requiring treatment. According to the WHO's classification 35 patients had Grade III and 24, Grade II oligodendrogliomas.

RESULTS

According to the intent to treat, patients were retrospectively classified in three groups as exclusive RT (Group 1), radio-chemotherapy (Group 2), or exclusive chemotherapy (Group 3). Median progression-free survival (PFS): was 47 months [95% confidence interval (CI) 39-56], and median overall survival (OS) was 109 months (95% CI 83-134). In univariate analysis, PFS was correlated with frontal location and WHO classification; OS was correlated with frontal location and Post-operative Karnosky performans status both appearing as independent prognostic factors for OS in multivariate analysis. There was no significant difference between the treatment groups with regard to PFS (P = 0.82) and OS (P = 0.64). In the group of patients treated with exclusive chemotherapy the 5-year PFS and OS rates were 44 and 71%, respectively.

CONCLUSION

Front-line exclusive chemotherapy results in prolonged OS in patients with confirmed pure oligodendroglioma. Whether this strategy improves quality of life remains debatable.

摘要

目的

少突胶质细胞瘤的最佳治疗方案仍不明确。尽管这些肿瘤对化疗敏感,但无法通过化疗治愈。我们研究了化疗是否能延迟放疗需求,同时不降低生存时长和质量。

方法与材料

1982年至1999年在里昂莱昂·贝拉尔中心接受少突胶质细胞瘤治疗的89例患者中,59例符合纳入标准,经中心审查为需要治疗的纯少突胶质细胞瘤。根据世界卫生组织分类,35例为Ⅲ级少突胶质细胞瘤,24例为Ⅱ级少突胶质细胞瘤。

结果

根据治疗意向,患者回顾性分为三组:单纯放疗组(第1组)、放化疗组(第2组)或单纯化疗组(第3组)。中位无进展生存期(PFS)为47个月[95%置信区间(CI)39 - 56],中位总生存期(OS)为109个月(95%CI 83 - 134)。单因素分析中,PFS与额叶位置及世界卫生组织分类相关;OS与额叶位置及术后卡诺夫斯基表现状态相关,二者在多因素分析中均为OS的独立预后因素。治疗组间PFS(P = 0.82)和OS(P = 0.64)无显著差异。在单纯化疗组患者中,5年PFS率和OS率分别为44%和71%。

结论

一线单纯化疗可延长确诊为纯少突胶质细胞瘤患者的总生存期。该策略是否能改善生活质量仍存在争议。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验