Ji Danyang, Lan Bo, Wang Jiayu, Ma Fei, Luo Yang, Li Qing, Zhang Pin, Cai Ruigang, Li Qiao, Chen Shanshan, Xu Binghe, Fan Ying
Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Thorac Cancer. 2025 Apr;16(7):e70035. doi: 10.1111/1759-7714.70035.
Pathological complete response (pCR) has been proven to be related to prognosis. pCR can be further classified as pCR of the breast (bpCR), pCR of axillary lymph nodes (apCR) or pCR of both tumors. The aim of this study was to elucidate the outcomes and clinicopathological characteristics associated with different patterns of pCR.
Patients with node-positive disease who received neoadjuvant chemotherapy between August 2009 and July 2016 and who achieved pCR in axillary lymph nodes, breast or both were included. Multivariate logistic regression was used to identify factors related to different patterns of pCR.
Among the 271 patients who were included in the study, 42.1% achieved total pCR, 46.1% achieved ApCR, and 11.8% achieved BpCR. Disease-free survival (DFS) was significantly better in the total pCR group than in the limited pCR groups throughout the entire cohort (p = 0.042). Univariate and multivariate analyses indicated that patients with HR-negative disease and a high Ki-67 proliferation index were more likely to achieve total pCR. Patients with earlier T stage disease were more likely to achieve pCR only in the breast. Among patients who achieved limited pCR, there was no significant difference in terms of whether these patients received intensified adjuvant chemotherapy.
Total pCR is still the best marker for predicting survival benefit in patients receiving neoadjuvant chemotherapy, and total pCR is more likely to be achieved in patients with HR-negative disease and a high Ki-67 proliferation index. T stage and N stage may predict apCR and bpCR, respectively.
病理完全缓解(pCR)已被证明与预后相关。pCR可进一步分为乳腺pCR(bpCR)、腋窝淋巴结pCR(apCR)或两者均为pCR。本研究的目的是阐明与不同pCR模式相关的结局和临床病理特征。
纳入2009年8月至2016年7月期间接受新辅助化疗且腋窝淋巴结、乳腺或两者均达到pCR的淋巴结阳性疾病患者。采用多因素逻辑回归分析确定与不同pCR模式相关的因素。
在纳入研究的271例患者中,42.1%达到完全pCR,46.1%达到ApCR,11.8%达到BpCR。在整个队列中,完全pCR组的无病生存期(DFS)显著优于局限性pCR组(p = 0.042)。单因素和多因素分析表明,激素受体(HR)阴性疾病和高Ki-67增殖指数的患者更有可能达到完全pCR。T分期较早的患者更有可能仅在乳腺达到pCR。在达到局限性pCR的患者中,是否接受强化辅助化疗没有显著差异。
完全pCR仍然是预测接受新辅助化疗患者生存获益的最佳指标,HR阴性疾病和高Ki-67增殖指数的患者更有可能达到完全pCR。T分期和N分期可能分别预测apCR和bpCR。