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21 基因复发评分检测在淋巴结阳性早期乳腺癌中的应用及 RxPONDER 试验对化疗决策的影响:临床医生是否已经做出决定?

The 21-Gene Recurrence Score Assay for Node-Positive, Early-Stage Breast Cancer and Impact of RxPONDER Trial on Chemotherapy Decision-Making: Have Clinicians Already Decided?

机构信息

Departments of Internal Medicine, University of Colorado, Aurora, Colorado

Departments of Radiation Oncology, University of Colorado, Aurora, Colorado

出版信息

J Natl Compr Canc Netw. 2017 Apr;15(4):494-503. doi: 10.6004/jnccn.2017.0049.

Abstract

The 21-gene recurrence score (RS) assay is retrospectively validated for assessing prognosis and benefit from chemotherapy in hormone receptor-positive, early-stage breast cancer (EBC) with low RS. We hypothesized that oncologists have already incorporated the RS assay for decision-making in higher-risk, node-positive disease, despite the lack of prospective data and contrary to NCCN Guideline recommendations. This study provides the first analysis of trends and differences in RS use and therapeutic implications in a population-based data set of patients with node-positive EBC. It also assesses the impact of the RxPONDER trial on clinicians' chemotherapy recommendations. Node-positive EBC cases diagnosed during 2010 through 2012 and included in the National Cancer Data Base were used. Multivariate logistic regression was used to estimate test use and impact on chemotherapy recommendations. The RS assay was ordered for 16.5% of the 80,405 identified patients. Of all variables, the RS assay had the strongest association with chemotherapy recommendation, with adjusted odds ratios (AORs) of 19 for scores >30. Odds of chemotherapy recommendation were significantly lower for the group who received the test (AOR, 0.21; 95% CI, 0.20-0.22). When divided based on the cutoff point of 25 adopted by the RxPONDER trial, those with an RS of 18 to 25 had significantly lower odds of chemotherapy recommendation compared with those with an RS of 26 to 30 (AOR, 0.32; 95% CI, 0.26-0.40). Test use was lower for blacks, community centers, uninsured/governmentally insured patients, higher tumor grade, larger tumor size, and more nodes involved. Chemotherapy recommendation was higher for patients of younger age, with private insurance, and with higher tumor grade, size, and number of nodes involved. Black patients had significantly higher RS (AOR, 1.37; 95% CI, 1.25-1.79). The RS assay influences clinicians' chemotherapy recommendation in node-positive EBC. Clinicians are using the inclusion criteria of the RxPONDER trial before its final release. Black patients have higher RS, likely representing worse biology. Significant differences exist in test use and clinical implications based on race, insurance, and facility.

摘要

21 基因复发评分 (RS) 检测已被回顾性验证,可用于评估激素受体阳性、低 RS 的早期乳腺癌 (EBC) 的预后和化疗获益。我们假设,尽管缺乏前瞻性数据且与 NCCN 指南建议相悖,肿瘤学家已经将 RS 检测纳入高风险、淋巴结阳性疾病的决策中。本研究首次分析了在淋巴结阳性 EBC 的基于人群的数据集的患者中 RS 使用的趋势和差异以及治疗意义。它还评估了 RxPONDER 试验对临床医生化疗建议的影响。

使用 2010 年至 2012 年期间诊断并包含在国家癌症数据库中的 80405 例确诊的淋巴结阳性 EBC 病例。多变量逻辑回归用于估计检测使用情况及其对化疗建议的影响。

RS 检测用于 80405 名患者中的 16.5%。在所有变量中,RS 检测与化疗建议的关联最强,评分>30 的调整优势比 (AOR) 为 19。接受检测的患者接受化疗的可能性显著降低 (AOR,0.21;95%CI,0.20-0.22)。根据 RxPONDER 试验采用的 25 个截止点进行划分时,RS 为 18 至 25 的患者与 RS 为 26 至 30 的患者相比,接受化疗的可能性显著降低 (AOR,0.32;95%CI,0.26-0.40)。黑人、社区中心、未投保/政府投保患者、较高的肿瘤分级、较大的肿瘤大小和更多的淋巴结受累,检测使用率较低。较年轻的患者、有私人保险的患者以及肿瘤分级、大小和淋巴结受累程度较高的患者,化疗建议较高。黑人患者的 RS 明显较高 (AOR,1.37;95%CI,1.25-1.79)。

RS 检测影响淋巴结阳性 EBC 患者的临床医生化疗建议。临床医生在 RxPONDER 试验最终发布之前使用其纳入标准。黑人患者的 RS 较高,可能代表更差的生物学。基于种族、保险和机构,检测使用和临床意义存在显著差异。

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