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一种新的用于单独接受全脑放疗(WBRT)的脑转移瘤患者的生存评分。

A new survival score for patients with brain metastases who received whole-brain radiotherapy (WBRT) alone.

机构信息

Department of Radiation Oncology, University of Lübeck, Germany.

出版信息

Radiother Oncol. 2013 Jul;108(1):123-7. doi: 10.1016/j.radonc.2013.06.009. Epub 2013 Jul 3.

Abstract

BACKGROUND AND PURPOSE

Survival scores for patients with brain metastasis exist. However, the treatment regimens used to create these scores were heterogeneous. This study aimed to develop and validate a survival score in homogeneously treated patients.

MATERIALS AND METHODS

Eight-hundred-and-eighty-two patients receiving 10 × 3Gy of WBRT alone were randomly assigned to a test group (N=441) or a validation group (N=441). In the multivariate analysis of the test group, age, performance status, extracranial metastasis, and systemic treatment prior to WBRT were independent predictors of survival. The score for each factor was determined by dividing the 6-month survival rate (in %) by 10. Scores were summed and total scores ranged from 6 to 19 points. Patients were divided into four prognostic groups.

RESULTS

The 6-month survival rates were 4% for 6-9 points, 29% for 10-14 points, 62% for 15-17 points, and 93% for 17-18 points (p<0.001) in the test group. The survival rates were 3%, 28%, 54% and 96%, respectively (p<0.001) in the validation group.

CONCLUSIONS

Since the 6-month survival rates in the validation group were very similar to the test group, this new score (WBRT-30) appears valid and reproducible. It can help making treatment choices and stratifying patients in future trials.

摘要

背景与目的

目前存在针对脑转移瘤患者的生存评分。然而,用于创建这些评分的治疗方案存在异质性。本研究旨在为接受同质治疗的患者开发和验证一种生存评分。

材料与方法

882 例接受 10×3Gy 单次全脑放疗(WBRT)的患者被随机分配至试验组(N=441)或验证组(N=441)。在试验组的多变量分析中,年龄、表现状态、颅外转移和 WBRT 前全身治疗是生存的独立预测因素。每个因素的评分通过将 6 个月生存率(%)除以 10 来确定。评分相加,总分为 6 至 19 分。患者被分为四个预后组。

结果

在试验组中,6-9 分、10-14 分、15-17 分和 17-18 分的 6 个月生存率分别为 4%、29%、62%和 93%(p<0.001)。在验证组中,生存率分别为 3%、28%、54%和 96%(p<0.001)。

结论

由于验证组的 6 个月生存率与试验组非常相似,因此该新评分(WBRT-30)似乎有效且可重复。它可以帮助做出治疗选择,并在未来的试验中对患者进行分层。

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