Dawood Shaheenah, Broglio Kristine, Kau Shu-Wan, Islam Rabiul, Symmans W Fraser, Buchholz Thomas A, McGuire Sean E, Meric-Bernstam Funda, Cristofanilli Massimo, Hortobágyi Gabriel N, Gonzalez-Angulo Ana M
Department of Breast Medical Oncology, Unit 1354, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030-4009, USA.
Oncologist. 2008 Jan;13(1):6-15. doi: 10.1634/theoncologist.2007-0107.
The aim of this retrospective study was to determine the prognostic impact of initial clinical stage in patients who achieved a pathological complete response (pCR) after receiving primary systemic chemotherapy (PST). Between 1977 and 2006, 489 patients who had achieved a pCR after receiving an anthracycline-based PST regimen were identified. Recurrence-free survival (RFS) and overall survival (OS) were estimated with the Kaplan-Meier product limit method and the differences between groups were compared using the log-rank statistic. Cox proportional hazards models were fit to determine the association of initial clinical stage with survival outcomes after adjusting for patient and tumor characteristics. The median age was 47 years. Twenty (4.1%) patients had stage I disease, 243 (49.7%) had stage II disease, 189 (38.7%) had stage III disease, and 37 (7.5%) had inflammatory breast cancer (IBC). At a median follow-up of 45 months, 59 (12%) patients had experienced disease recurrence. The 5-year RFS and OS rates for the whole cohort were 87.8% and 89.3%, respectively. Lower clinical stage at diagnosis was associated with statistically significant higher RFS and OS rates. In a multivariate model, patients with clinical stage IIIB/C disease and those with IBC had lower RFS rates than patients with clinical stage I/II/IIIA disease. In addition, patients with clinical stage IIIB/C disease and those with IBC had a greater hazard of death than patients with clinical stage I/II/IIIA disease. Overall, patients who achieved a pCR had a low rate of recurrence. However, higher clinical stage and IBC were associated with worse outcomes in breast cancer patients who achieved a pCR after PST.
本回顾性研究的目的是确定接受原发性全身化疗(PST)后达到病理完全缓解(pCR)的患者初始临床分期对预后的影响。在1977年至2006年期间,共识别出489例接受基于蒽环类药物的PST方案后达到pCR的患者。采用Kaplan-Meier乘积限法估计无复发生存期(RFS)和总生存期(OS),并使用对数秩统计量比较组间差异。拟合Cox比例风险模型以确定在调整患者和肿瘤特征后初始临床分期与生存结果之间的关联。中位年龄为47岁。20例(4.1%)患者为I期疾病,243例(49.7%)为II期疾病,189例(38.7%)为III期疾病,37例(7.5%)为炎性乳腺癌(IBC)。中位随访45个月时,59例(12%)患者出现疾病复发。整个队列的5年RFS率和OS率分别为87.8%和89.3%。诊断时较低的临床分期与统计学上显著较高的RFS率和OS率相关。在多变量模型中,临床IIIB/C期疾病患者和IBC患者的RFS率低于临床I/II/IIIA期疾病患者。此外,临床IIIB/C期疾病患者和IBC患者的死亡风险高于临床I/II/IIIA期疾病患者。总体而言,达到pCR的患者复发率较低。然而,较高的临床分期和IBC与PST后达到pCR的乳腺癌患者的较差预后相关。