Abstract

The long-term effect of axillary pathologic complete response (pCR) on survival among women with breast cancer treated with primary systemic chemotherapy (PST) is unknown. To assess the long-term effect of axillary pCR on relapse-free survival (RFS) and overall survival (OS) in women with breast cancer with cytologically confirmed axillary lymph node metastases treated with PST. We retrospectively analyzed the effect of axillary pCR on 10-year OS and RFS among all women who received a diagnosis of breast cancer stages II to III with cytologically confirmed axillary metastases between 1989 and 2007 who received PST at a large US comprehensive cancer center. Women were stratified by post-PST axillary status, and survival outcomes were estimated and compared according to response in the breast and axilla. Outcomes of interest were RFS and OS. Of 1600 women treated, median (range) age at diagnisis was 49 (21-86) years. A total of 454 (28.4%) achieved axillary pCR. These patients were more likely to have human epidermal growth factor receptor 2 (HER2)-positive and triple-negative disease (P < .001), pCR in the breast (P < .001), high-grade tumors (P < .001), and lower clinical and pathologic T stage (P = .002). Ten-year OS rates were 84% (95% CI, 79%-88%) and 57% (95% CI, 54%-61%) (P < .001) and 10-year RFS rates 79% (95% CI, 74%-83%) and 50% (95% CI, 46%-53%) (P < .001) for patients with axillary pCR and residual axillary disease, respectively. For patients with axillary pCR, 10-year OS rates were 90% (95% CI, 84%-94%) for those with breast pCR and 72% (95% CI, 61%-80%) for those with residual breast disease (P < .001). For patients with residual axillary disease, 10-year OS rates were 66% (95% CI, 56%-74%) for patients with and 56% (95% CI, 52%-60%) for patients without breast pCR (P = .02). Of patients receiving HER2-targeted therapy for HER2-positive disease, 67.1% (100 of 149) achieved axillary pCR; 10-year OS rates were 92% (95% CI, 84%-96%) and 57% (95% CI, 20%-82%) (P = .003) and 10-year RFS rates 89% (95% CI, 81%-94%) and 44% (95% CI, 18%-68%) (P < .001) for those with axillary pCR and residual axillary disease, respectively. Axillary pCR was associated with improved 10-year OS and RFS. Patients with axillary and breast pCR after PST had superior long-term survival outcomes. Patients undergoing HER2-targeted therapy for HER2-positive disease had high rates of axillary pCR, and those with axillary pCR had excellent 10-year OS.

Highlights

  • MethodsHormone receptor [hormone receptor (HR)] and human epidermal growth factor receptor 2 (HER2) status), tumor and lymph node clinical and pathologic staging (according to the American Joint Committee on Cancer/International Union Against Cancer TNM staging classification) nuclear grade, adjuvant therapies (additional chemotherapy, radiation therapy, and endocrine therapy), and class of primary systemic chemotherapy (PST) used (anthracycline-based only, taxane-based only, or containing both an anthracycline and a taxane)

  • Primary systemic chemotherapy has been shown to be equivalent to adjuvant chemotherapy in terms of overall survival (OS) and relapse-free survival (RFS),[1,2] and use of primary systemic chemotherapy (PST) increases the rates of breast conservation surgery

  • Several studies have shown that patients treated with PST who achieve a pathologic complete response in the breast and axilla have superior longterm outcomes.[2,3,4]

Read more

Summary

Methods

Hormone receptor [HR] and HER2 status), tumor and lymph node clinical and pathologic staging (according to the American Joint Committee on Cancer/International Union Against Cancer TNM staging classification) nuclear grade, adjuvant therapies (additional chemotherapy, radiation therapy, and endocrine therapy), and class of PST used (anthracycline-based only, taxane-based only, or containing both an anthracycline and a taxane). Breast pCR (T0 disease) was defined as no residual invasive carcinoma; residual intraductal carcinoma alone was classified as T0. Race and ethnicity were collected by selfreport by questionnaire at the time of new patient visit and are included to demonstrate the diversity of patients seen at our institution. The institutional review board of the University of Texas MD Anderson Cancer Center approved this study. Informed consent was waived due to the retrospective nature of this study

Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call