Unit of Oncology 1, Department of Oncology, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Unit of Oncology 1, Department of Oncology, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Eur J Cancer. 2019 Sep;118:121-130. doi: 10.1016/j.ejca.2019.06.008. Epub 2019 Jul 19.
Despite the well-known negative prognostic value of the BRAF mutation in patients with metastatic colorectal cancer (mCRC), its outcome is quite heterogeneous, and the basis for this prognostic heterogeneity should be better defined.
Two large retrospective series of BRAF-mutated mCRC from 22 institutions served as an exploratory and validation set to develop a prognostic score. The model was internally and externally validated.
A total of 395 BRAF-mutated mCRCs were included in the exploratory set. Performance status, CA19.9, lactate dehydrogenase, neutrophil/lymphocyte ratio, grading and liver, lung and nodal involvement emerged as independent prognostic factors for overall survival (OS). Two different scoring systems were built: a 'complete' score (0-16) including all significant covariates and a 'simplified' score (0-9), based only on clinicopathological covariates, and excluding laboratory values. Adopting the complete score, proportions of patients with a low (0-4), intermediate (5-8) and high (9-16) score were 44.7%, 42.6% and 12.6%, respectively. The median OS was 29.6, 15.5 (hazard ratio [HR] for intermediate vs low risk: 2.16, 95% confidence interval [CI]: 1.44-3.22, p < .001) and 6.6 months (HR for high vs low risk: 4.72, 95% CI: 2.72-8.20, p < .001). Similar results were observed also after adjusting for the type of first-line treatment and adopting the simplified score. The simplified prognostic score derived from the exploratory set was then applied to the validation set for external confirmation.
These scoring systems are based on easy-to-collect data and defined specific subgroups with relevant differences in their life expectancy. These tools could be useful in clinical practice, would allow better stratification of patients in clinical trials and may be adopted for proper adjustments in exploratory translational analyses.
尽管 BRAF 突变对转移性结直肠癌(mCRC)患者具有众所周知的不良预后价值,但其实验室结果存在较大的异质性,需要进一步明确这种预后异质性的基础。
本研究利用 22 个机构的两个大型 BRAF 突变 mCRC 回顾性队列作为探索性和验证性队列,以开发预后评分系统。该模型经过内部和外部验证。
共纳入 395 例 BRAF 突变 mCRC 患者,分析结果显示体能状态、CA19.9、乳酸脱氢酶、中性粒细胞与淋巴细胞比值、分级以及肝脏、肺部和淋巴结转移是总生存的独立预后因素。本研究构建了两个不同的评分系统:包括所有显著协变量的“完整”评分(0-16 分)和仅基于临床病理协变量的“简化”评分(0-9 分),同时排除了实验室检查结果。采用完整评分,低(0-4 分)、中(5-8 分)和高(9-16 分)风险评分患者的比例分别为 44.7%、42.6%和 12.6%。中位总生存期分别为 29.6、15.5 个月(中危 vs 低危风险比:2.16,95%置信区间:1.44-3.22,p<0.001)和 6.6 个月(高危 vs 低危风险比:4.72,95%置信区间:2.72-8.20,p<0.001)。在调整一线治疗类型后,也观察到了类似的结果。随后,在验证性队列中应用探索性队列中建立的简化预后评分系统进行外部验证。
这些评分系统基于易于收集的数据,定义了具有不同预期寿命的特定亚组。这些工具在临床实践中可能具有一定的应用价值,有助于更好地对患者进行临床试验分层,并且可以用于探索性转化分析的适当调整。