Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY, 10065, USA.
Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Breast Cancer Res Treat. 2024 Jan;203(1):153-161. doi: 10.1007/s10549-023-07127-3. Epub 2023 Sep 28.
The 21-gene recurrence score (RS) assay predicts the recurrence risk and magnitude of chemotherapy benefit in patients with invasive breast cancer (BC). This study examined low-grade tumors yielding a high-risk RS and their outcomes.Kindly check the edit made in the article titleOk METHODS: We compared patients with grade 1 BC and a high-risk RS to those with low-risk RS. Histologic sections were reviewed and features reported to elevate the RS were noted, mainly biopsy cavity and reactive stromal changes (BXC).
A total of 54 patients had high-risk RS (median RS of 28, range 26-36). On review, BXC were seen in all cases. Thirty BCs in this group also had low to negative PR. Treatment regimens included: chemoendocrine therapy (63%), endocrine therapy alone (31%) and no adjuvant therapy (6%). There were no additional breast cancer events over a median follow-up of 54.0 months (range 6.2 to 145.3). A total of 108 patients had low-risk RS (median RS of 7, range 0-9). BXC were seen in 47% of cases and none were PR negative. One patient had a recurrence at 64.8 months while the rest had no additional events over a median of 68.1 months (2.4 to 100).
We provide further evidence that reactive stromal changes and/or low-PR scores enhance the elevation of the RS. A high-RS result in low grade, PR-positive BC may not reflect actual risk and any suspected discrepancies should be discussed with the management teams. Multigene testing results should be interpreted after correlation with pathologic findings to optimize patient care.
21 基因复发评分 (RS) 检测可预测浸润性乳腺癌 (BC) 患者的复发风险和化疗获益程度。本研究探讨了低级别肿瘤中 RS 高风险的情况及其结局。
我们比较了 RS 高风险的 1 级 BC 患者与 RS 低风险的患者。回顾组织学切片,记录了升高 RS 的特征,主要是活检腔和反应性间质改变 (BXC)。
共有 54 例患者 RS 高风险(中位 RS 为 28,范围 26-36)。回顾时,所有病例均可见 BXC。该组中有 30 例 BC 低表达或阴性 PR。治疗方案包括:化疗内分泌治疗 (63%)、内分泌治疗单独 (31%)和无辅助治疗 (6%)。中位随访 54.0 个月(范围 6.2-145.3)后,未发生额外的乳腺癌事件。共有 108 例患者 RS 低风险(中位 RS 为 7,范围 0-9)。BXC 见于 47%的病例,无 PR 阴性病例。1 例患者在 64.8 个月时复发,其余患者在中位随访 68.1 个月(2.4-100)期间无其他事件。
我们提供了进一步的证据表明反应性间质改变和/或低 PR 评分可增强 RS 的升高。高 RS 结果在低级别、PR 阳性的 BC 中可能无法反映实际风险,任何可疑差异都应与管理团队讨论。多基因检测结果应与病理结果相关联进行解释,以优化患者的治疗。