Division of Breast and Melanoma Surgical Oncology, Department of Surgery, Mayo Clinic, Rochester, MN, USA.
Division of Clinical Trials and Biostatistics, Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Ann Surg Oncol. 2024 Aug;31(8):5132-5140. doi: 10.1245/s10434-024-15583-4. Epub 2024 Jun 13.
For operable triple-negative breast cancer (TNBC) treated with neoadjuvant chemotherapy (NAC), clinical prognostication and postoperative decision-making relies exclusively on whether a pathologic complete response (pCR) is achieved or not. We evaluated whether extent of disease at presentation further influenced overall survival (OS) among patients with pCR or with residual disease (RD) following NAC.
Patients with stage I-III TNBC who underwent NAC were identified from the National Cancer Database from 2010 to 2019. Overall survival was assessed by disease extent using the Kaplan-Meier method and Cox proportional hazards regression for univariate and multivariable analysis.
A total of 35,598 patients met inclusion criteria, and 11,967 achieved pCR. Ten-year OS was 88.5% and varied by cT and cN category at presentation. Best 10-year OS was seen in patients with cT1-2, cN0 (90.9%) and was worst in those with cT3-4, cN2-3 disease (72.0%). A total of 23,631 patients had RD. Ten-year OS was 60.1% and varied by cT and cN category at presentation. Best 10-year OS was seen in patients with cT1-2, cN0 (73.0%) and was worst in those with cT3-4, cN2-3 disease (36.3%). Notably, OS was significantly poorer for patients with cT3-4, cN2-3 disease at diagnosis and pCR versus those with cT1-2 cN0 and RD (aHR 1.30, 95% confidence interval 1.03-1.63, p = 0.03).
Among patients with TNBC, extent of disease at presentation was prognostic for OS independently of response to NAC. Patients with advanced stage at presentation had poorer OS even in the context of pCR. Further investigation is needed to evaluate whether additional adjuvant therapy strategies should be considered for these patients.
对于接受新辅助化疗(NAC)治疗的可手术三阴性乳腺癌(TNBC),临床预后和术后决策完全依赖于是否达到病理完全缓解(pCR)。我们评估了在接受 NAC 后达到 pCR 或有残留疾病(RD)的患者中,疾病程度是否进一步影响总生存期(OS)。
从 2010 年至 2019 年,从国家癌症数据库中确定了接受 NAC 的 I-III 期 TNBC 患者。使用 Kaplan-Meier 方法评估疾病程度对总生存期的影响,并使用 Cox 比例风险回归进行单因素和多因素分析。
共有 35598 名患者符合纳入标准,其中 11967 名患者达到 pCR。10 年 OS 为 88.5%,并随就诊时 cT 和 cN 分类而变化。cT1-2、cN0 患者的最佳 10 年 OS 为 90.9%,而 cT3-4、cN2-3 疾病患者的最差为 72.0%。共有 23631 名患者有 RD。10 年 OS 为 60.1%,并随就诊时 cT 和 cN 分类而变化。cT1-2、cN0 患者的最佳 10 年 OS 为 73.0%,而 cT3-4、cN2-3 疾病患者的最差为 36.3%。值得注意的是,与 cT1-2、cN0 和 RD 患者相比,诊断时 cT3-4、cN2-3 疾病和 pCR 的患者 OS 显著更差(aHR 1.30,95%置信区间 1.03-1.63,p=0.03)。
在 TNBC 患者中,就诊时的疾病程度是 OS 的独立预后因素,与 NAC 的反应无关。就诊时处于晚期的患者,即使达到 pCR,其 OS 也较差。需要进一步研究评估是否应考虑为这些患者制定额外的辅助治疗策略。