Mayo Clinic Florida, Jacksonville, FL.
Division of Biomedical Statistics and Informatics, Mayo Clinic, Jacksonville, FL.
J Natl Compr Canc Netw. 2024 Aug 26;22(7):463-468. doi: 10.6004/jnccn.2024.7015.
The Clinical Treatment Score post-5 years (CTS5) is a risk stratification tool used to determine the risk of late recurrence in hormone receptor-positive (HR+), HER2-negative breast cancer (BC). Limited data exist on its use in HR+, HER2-positive (HER2+) BC.
CTS5 was evaluated in HR+, HER2+ BC in the North Central Cancer Treatment Group (NCCTG) N9831 (Alliance) and NSABP B-31 (NRG) trials.
A total of 1,862 patients with HR+, HER2+ BC without recurrence 5 years after enrollment were included. Overall, the CTS5 score was significantly associated with recurrence-free survival (RFS), with a hazard ratio (HR) of 1.35 (95% CI, 1.12-1.63; P=.002), but did not reach statistical significance in patients who received trastuzumab (n=829; HR, 1.29; 95% CI, 0.98-1.71; P=.07). CTS5 risk category was not significantly associated with RFS. In patients who received trastuzumab, other variables used in CTS5, including patient age and tumor size, were not significantly associated with RFS. N3 was significantly associated with worse outcomes (HR, 1.86; 95% CI, 1.09-3.17; P=.02) compared with N0-N1. Paradoxically, higher tumor grade was associated with better outcomes after 5 years in the multivariate analysis (HR, 0.71; 95% CI, 0.50-1.00; P=.05). The incidence of recurrences or deaths between years 5 to 10 was 10.6% in the CTS5 low-risk category, 5.6% in the intermediate-risk category, and 9.8% in the high-risk category.
The CTS5 model does not accurately predict the risk of late recurrence in HR+, HER2+ BC treated with adjuvant trastuzumab in the N9831 and B-31 trials. This study underlines the need to develop a new prognostic model to better delineate the risk of late recurrence in patients with HR+, HER2+ BC receiving adjuvant trastuzumab.
gov identifiers: NCT00005970 (NCCTG N9831) and NCT00004067 (NRG/NSABP B-31).
临床治疗评分 5 年后(CTS5)是一种风险分层工具,用于确定激素受体阳性(HR+)、HER2 阴性(HER2-)乳腺癌(BC)患者发生晚期复发的风险。目前,关于其在 HR+、HER2+BC 中的应用,仅有有限的数据。
在 NCCTG N9831(Alliance)和 NSABP B-31(NRG)试验中,对 HR+、HER2+BC 患者进行了 CTS5 评估。
共纳入 1862 例 HR+、HER2+BC 患者,在入组后 5 年内无复发。总体而言,CTS5 评分与无复发生存(RFS)显著相关,风险比(HR)为 1.35(95%CI,1.12-1.63;P=.002),但在接受曲妥珠单抗治疗的患者中未达到统计学意义(n=829;HR,1.29;95%CI,0.98-1.71;P=.07)。CTS5 风险类别与 RFS 无显著相关性。在接受曲妥珠单抗治疗的患者中,CTS5 中使用的其他变量,包括患者年龄和肿瘤大小,与 RFS 无显著相关性。与 N0-N1 相比,N3 与较差的预后显著相关(HR,1.86;95%CI,1.09-3.17;P=.02)。然而,在多变量分析中,肿瘤分级较高与 5 年后的较好预后相关(HR,0.71;95%CI,0.50-1.00;P=.05)。在 CTS5 低危组、中危组和高危组中,5 至 10 年内复发或死亡的发生率分别为 10.6%、5.6%和 9.8%。
在 N9831 和 B-31 试验中,CTS5 模型不能准确预测接受辅助曲妥珠单抗治疗的 HR+、HER2+BC 患者的晚期复发风险。这项研究强调需要开发新的预后模型,以更好地区分接受辅助曲妥珠单抗治疗的 HR+、HER2+BC 患者的晚期复发风险。
gov 标识符:NCT00005970(NCCTG N9831)和 NCT00004067(NRG/NSABP B-31)。