Massachusetts General Hospital Cancer Center, Boston, Massachusetts.
Harvard Medical School, Boston, Massachusetts.
Clin Cancer Res. 2020 Jun 15;26(12):2838-2848. doi: 10.1158/1078-0432.CCR-19-3492. Epub 2020 Feb 11.
While various studies have highlighted the prognostic significance of pathologic complete response (pCR) after neoadjuvant chemotherapy (NAT), the impact of additional adjuvant therapy after pCR is not known.
PubMed was searched for studies with NAT for breast cancer and individual patient-level data was extracted for analysis using plot digitizer software. HRs, with 95% probability intervals (PI), measuring the association between pCR and overall survival (OS) or event-free survival (EFS), were estimated using Bayesian piece-wise exponential proportional hazards hierarchical models including pCR as predictor.
Overall, 52 of 3,209 publications met inclusion criteria, totaling 27,895 patients. Patients with a pCR after NAT had significantly better EFS (HR = 0.31; 95% PI, 0.24-0.39), particularly for triple-negative (HR = 0.18; 95% PI, 0.10-0.31) and HER2 (HR = 0.32; 95% PI, 0.21-0.47) disease. Similarly, pCR after NAT was also associated with improved survival (HR = 0.22; 95% PI, 0.15-0.30). The association of pCR with improved EFS was similar among patients who received subsequent adjuvant chemotherapy (HR = 0.36; 95% PI, 0.19-0.67) and those without adjuvant chemotherapy (HR = 0.36; 95% PI, 0.27-0.54), with no significant difference between the two groups ( = 0.60).
Achieving pCR following NAT is associated with significantly better EFS and OS, particularly for triple-negative and HER2 breast cancer. The similar outcomes with or without adjuvant chemotherapy in patients who attain pCR likely reflects tumor biology and systemic clearance of micrometastatic disease, highlighting the potential of escalation/deescalation strategies in the adjuvant setting based on neoadjuvant response..
尽管多项研究强调了新辅助化疗(NAT)后病理完全缓解(pCR)的预后意义,但 pCR 后辅助治疗的影响尚不清楚。
在 PubMed 上搜索了关于乳腺癌的 NAT 研究,并使用 Plot Digitizer 软件提取个体患者水平的数据进行分析。使用贝叶斯分段指数比例风险层次模型,将 pCR 作为预测因子,估计 HRs(95%概率区间(PI)),以衡量 pCR 与总生存(OS)或无事件生存(EFS)之间的关联。
共有 52 篇 3209 篇文献符合纳入标准,共纳入 27895 例患者。NAT 后 pCR 的患者 EFS 明显更好(HR=0.31;95%PI,0.24-0.39),尤其是三阴性(HR=0.18;95%PI,0.10-0.31)和 HER2(HR=0.32;95%PI,0.21-0.47)疾病。同样,NAT 后 pCR 也与生存改善相关(HR=0.22;95%PI,0.15-0.30)。在接受辅助化疗的患者(HR=0.36;95%PI,0.19-0.67)和未接受辅助化疗的患者(HR=0.36;95%PI,0.27-0.54)中,pCR 与改善的 EFS 相关,两组之间无显著差异(=0.60)。
NAT 后达到 pCR 与 EFS 和 OS 显著改善相关,特别是对三阴性和 HER2 乳腺癌。在达到 pCR 的患者中,无论是否接受辅助化疗,其结局相似,这可能反映了肿瘤生物学和微转移疾病的全身清除,强调了基于新辅助反应的辅助治疗中升级/降级策略的潜力。