4.6 Article

New validated prognostic models and prognostic calculators in patients with low-grade gliomas diagnosed by central pathology review: a pooled analysis of EORTC/RTOG/NCCTG phase III clinical trials

期刊

NEURO-ONCOLOGY
卷 15, 期 11, 页码 1568-1579

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/neuonc/not117

关键词

low-grade glioma; predictive accuracy; prognostic factors

资金

  1. National Cancer Institute (NCI) [2U10CA11488-16, 2U10CA11488-17, 2U10CA11488-18, 2U10CA11488-19, 2U10CA11488-20, 2U10CA11488-21, 2U10CA11488-22, 2U10CA11488-23, 2U10CA11488-24, 2U10CA11488-25, 2U10CA11488-26, 2U10CA11488-27, 2U10CA11488-28]
  2. National Cancer Institute (NCI). [2U10CA11488-29, 2U10CA11488-30, 2U10CA11488-31, 2U10CA11488-32, 2U10CA11488-33, 2U10CA11488-34, 2U10CA11488-35, 2U10CA11488-36, 2U10CA11488-37, 2U10CA11488-38, 2U10CA11488-39, 2U10CA11488-40, 2U10 CA011488-41, U10 CA21661, U10 CA37422]

向作者/读者索取更多资源

In a previous study, the European Organisation for Research and Treatment of Cancer (EORTC) reported a scoring system to predict survival of patients with low-grade gliomas (LGGs). A major issue in the diagnosis of brain tumors is the lack of agreement among pathologists. New models in patients with LGGs diagnosed by central pathology review are needed. Data from 339 EORTC patients with LGGs diagnosed by central pathology review were used to develop new prognostic models for progression-free survival (PFS) and overall survival (OS). Data from 450 patients with centrally diagnosed LGGs recruited into 2 large studies conducted by North American cooperative groups were used to validate the models. Both PFS and OS were negatively influenced by the presence of baseline neurological deficits, a shorter time since first symptoms (30 wk), an astrocytic tumor type, and tumors larger than 5 cm in diameter. Early irradiation improved PFS but not OS. Three risk groups have been identified (low, intermediate, and high) and validated. We have developed new prognostic models in a more homogeneous LGG population diagnosed by central pathology review. This population better fits with modern practice, where patients are enrolled in clinical trials based on central or panel pathology review. We could validate the models in a large, external, and independent dataset. The models can divide LGG patients into 3 risk groups and provide reliable individual survival predictions. Inclusion of other clinical and molecular factors might still improve models predictions.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据