Department of Surgery, Division of Surgical Oncology, University of Louisville, Louisville, KY.
Department of Surgery, Division of Surgical Oncology, Kaiser Permanente Sacramento, Sacramento, CA.
Surgery. 2019 Oct;166(4):509-514. doi: 10.1016/j.surg.2019.04.044. Epub 2019 Jul 20.
Broad patterns of use of the gene signature panel Oncotype DX DCIS and its large-scale impact on postoperative administration of radiation therapy in women with ductal carcinoma in situ of the breast remain unclear. This study sought to evaluate the patterns of use of this gene signature panel in women with ductal carcinoma in situ and the impact of these tools on postoperative radiation therapy administration.
The National Cancer Database was queried for women with ductal carcinoma in situ treated with breast-conserving therapy who had information regarding whether a gene signature panel was performed between 2010 and 2015. Demographic characteristics, the characteristics of their ductal carcinoma in situ, and whether they received postoperative radiation therapy were compared among patients who did have a gene signature panel performed and those who did not. Patterns of radiation therapy administration were also evaluated based on the recurrence risk score by the gene signature panel.
Gene signature panel use increased over time, with a sharp increase in utilization occurring in 2015 (8.0% in 2015 vs 4.4% in 2014, P < .001). Patients with estrogen receptor-positive ductal carcinoma in situ were somewhat more likely to have a gene signature panel ordered (3.9% estrogen receptor positive vs 1.7% estrogen receptor negative, P < .001), as were patients with lower-grade ductal carcinoma in situ (4.5% grade I/II vs 3.1% grade III, P < .001). Gene signature panel utilization was associated with a decrease in the administration of postoperative radiation therapy (48.6% gene signature panel vs 83.4% no gene signature panel, P < .001). Among patients in whom a gene signature panel was performed, postoperative radiation therapy was administered in 81.9%, 72.0%, and 35.9% of patients with high-, intermediate-, and low-recurrence scores, respectively.
Gene signature panel use in patients with ductal carcinoma in situ has increased over time and is more commonly used in women with lower-risk, clinicopathologic features to determine the magnitude of benefit afforded by radiation therapy. Gene signature panel use is associated with decreased rates of postoperative radiation therapy administration, particularly among patients with scores suggesting a low rate of recurrence.
Oncotype DX DCIS 基因标记面板的广泛使用模式及其对接受保乳治疗的乳腺导管原位癌女性术后放射治疗的大规模影响仍不清楚。本研究旨在评估该基因标记面板在乳腺导管原位癌患者中的使用模式,以及这些工具对术后放射治疗的影响。
利用国家癌症数据库,对 2010 年至 2015 年间接受保乳治疗且有基因标记面板检查信息的乳腺导管原位癌患者进行了查询。比较了进行基因标记面板检查和未进行基因标记面板检查的患者的人口统计学特征、导管原位癌特征,以及是否接受术后放射治疗。还根据基因标记面板的复发风险评分评估了放射治疗的管理模式。
基因标记面板的使用随着时间的推移而增加,在 2015 年出现了急剧增加(2015 年为 8.0%,2014 年为 4.4%,P<0.001)。雌激素受体阳性的乳腺导管原位癌患者更有可能接受基因标记面板的检查(雌激素受体阳性患者为 3.9%,雌激素受体阴性患者为 1.7%,P<0.001),低分级的乳腺导管原位癌患者也更有可能接受基因标记面板的检查(I/II 级患者为 4.5%,III 级患者为 3.1%,P<0.001)。基因标记面板的使用与术后放射治疗的减少相关(基因标记面板组为 48.6%,无基因标记面板组为 83.4%,P<0.001)。在进行基因标记面板检查的患者中,高、中、低复发评分的患者分别有 81.9%、72.0%和 35.9%接受了术后放射治疗。
随着时间的推移,乳腺导管原位癌患者中基因标记面板的使用有所增加,并且更常用于低风险、临床病理特征的女性,以确定放射治疗的获益程度。基因标记面板的使用与术后放射治疗的使用率降低有关,尤其是在评分提示复发率低的患者中。