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首页> 外文期刊>The oncologist >Evaluation of the Incorporation of Recurrence Score into the American Joint Committee on Cancer Eighth Edition Staging System in Patients with T1-2N0M0, Estrogen Receptor-Positive, Human Epidermal Growth Receptor 2-Negative Invasive Breast Cancer: A Population-Based Analysis
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Evaluation of the Incorporation of Recurrence Score into the American Joint Committee on Cancer Eighth Edition Staging System in Patients with T1-2N0M0, Estrogen Receptor-Positive, Human Epidermal Growth Receptor 2-Negative Invasive Breast Cancer: A Population-Based Analysis

机译:在T1-2N0M0,雌激素受体阳性,人体表皮生长受体2阴性侵袭性乳腺癌中将复发评分纳入美国联合委员会纳入美国联合委员会的评估:基于人群的分析

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Background The current study aimed to evaluate the predictive performance of the American Joint Committee on Cancer eighth edition staging system in patients with invasive breast cancer based on the Surveillance, Epidemiology, and End Results database. Subjects, Materials, and Methods Patients diagnosed with T1-2N0M0, estrogen receptor-positive, human epidermal growth factor receptor 2-negative breast cancer from 2010 to 2014 were retrospectively recruited in this analysis. Patients were reassigned to different stages according to the anatomic staging system (AS), prognostic staging system (PS), and prognostic and genomic staging criteria downstaging patients with recurrence score (RS) lower than 11 (PGS_RS11). Cox models were conducted for multivariate analyses, and likelihood ratio (LR) χ 2 , Akaike information criterion (AIC), and Harrell's concordance index (C-index) were calculated for the comparison of different staging systems. Additionally, adjustments were made to generate prognostic and genomic staging criteria downstaging patients with RS lower than 18 (PGS_RS18) and RS lower than 25 (PGS_RS25). Results PGS_RS11 was an independent predictor for breast cancer-specific survival, as were PS and AS. Adjusted for age and ethnicity, PGS_RS11 (AIC = 2,322.763, C-index = 0.7482, LR χ 2 = 113.17) showed superiority in predicting survival outcomes and discriminating patients compared with AS (AIC = 2,369.132, C-index = 0.6986, LR χ 2 = 60.80) but didn't outperform PS (AIC = 2,320.992, C-index = 0.7487, LR χ 2 = 114.94). The predictive and discriminative ability of PGS_RS18 was the best (AIC = 2297.434, C-index = 0.7828, LR χ 2 = 138.50) when compared with PS and PGS_RS11. Conclusion PGS_RS11 was superior to AS but comparable with PS in predicting prognosis. Further validations and refinements are needed for the better incorporation of RS into staging systems. Implications for Practice Staging systems are of critical importance in informing prognosis and guiding treatment. This study's objective was to evaluate the newly proposed staging system in the American Joint Committee on Cancer eighth edition staging manual, which combined biological and genomic information with the traditional TNM classification for the first time to determine tumor stages of breast cancer. The superiority of the prognostic and genomic staging system was validated in our cohort and possibly could encourage the utility of genomic assays in clinical practice for staging assessment and prognosis prediction.
机译:背景技术目前的研究旨在根据监测,流行病学和最终结果数据库评估患有侵袭性乳腺癌患者癌症第八版分期系统的预测性能。在本分析中回顾性招募了患有T1-2N0M0,雌激素受体阳性,雌激素受体阳性,人表皮生长因子受体2阴性乳腺癌的患者。根据解剖学分期系统(AS),预后分期系统(PS),预后和基因组分期标准的衰退患者低于11(PGS_RS11),重新分期为不同阶段。为了多变量分析进行了COX模型,并且计算了似然比(LR)χ2,Akaike信息标准(AIC)和Harrell的一致性指数(C-Index)用于不同分期系统。另外,调整是在低于18(PGS_RS18)和低于25(PGS_RS25)的下降患者的预后和基因组分期标准的调整。结果PGS_RS11是乳腺癌特异性存活的独立预测因子,如PS和AS。调整为年龄和种族,PGS_RS11(AIC = 2,322.763,C-Index = 0.7482,LR≥2= 113.17)在预测存活结果和鉴别患者的情况下,与(AIC = 2,369.132,C-Index = 0.6986,LRχ2 = 60.80)但没有胜过PS(AIC = 2,320.992,C-Index = 0.7487,LRχ2 = 114.94)。与PS和PGS_RS11相比,PGS_RS18的预测性和鉴别能力是最佳的(AIC = 2297.434,C-INDEX = 0.7828,LR≥2= 138.50)。结论PGS_RS11优于预测预后PS。需要更好地纳入分期系统所需的进一步验证和改进。对实践分期系统的影响对于告知预后和指导治疗的重要性是至关重要的。本研究的目标是评估美国联合癌症第八版分期手册中的新提议的分期系统,这是第一次确定传统的TNM分类的生物和基因组信息,以确定乳腺癌的肿瘤阶段。在我们的队列中验证了预后和基因组分期系统的优越性,并且可能鼓励基因组测定在分期评估和预后预测中的临床实践中的效用。

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