Adjuvant taxane therapy for early-stage breast cancer: A real-world comparison of chemotherapy regimens in Ontario.

Authors

null

Sofia Torres

Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, ON, Canada

Sofia Torres , Maureen E. Trudeau , Andrea Eisen , Craig Earle , Kelvin K. Chan

Organizations

Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, ON, Canada, Sunnybrook Odette Cancer Centre, University of Toronto, Toronto, ON, Canada, Institute for Clinical Evaluative Sciences, Toronto, ON, Canada

Research Funding

No funding sources reported

Background: FEC-D (5-FU, epirubicin, cyclophosphamide - docetaxel) and dd (dose-dense) AC-P (doxorubicin-cyclophosphamide - paclitaxel) are considered equally effective regimens in the adjuvant treatment of breast cancer (BC), although never compared directly in a clinical trial. We compared the outcome of BC patients (pts) treated with FEC-D, dd AC-P and AC-P (q3 weekly). Methods: Retrospective study including all female BC pts diagnosed in 2003-2009 in Ontario, who received 1 of those regimens (ascertained from New Drug Funding Program and physician claims databases). Primary endpoint: overall survival (OS). Secondary endpoints: emergency room (ER) visits/admissions, risk of heart failure (HF). Analysis were conducted for OS and HF using Kaplan-Meier method and adjusted for confounders using proportional hazard models. Multivariable logistic regressions were performed for ER visits/admissions adjusting for confounders. FEC-D and ddAC-P were compared using propensity score (PS) matching. Results: 8,462 pts were identified, 4,710 (55.7%) received FEC-D, 2,065 (24.4%) AC-P and 1,687 (19.9%) dd AC-P. Patient characteristics were imbalanced between the arms. In unadjusted analyses, 5-year OS was 91.7% for FEC-D, 89.0% for dd AC-P and 87.4% for AC-P; after PS matching, it was 92% for FEC-D and 89% for ddAC-P. After adjusting for confounders, risk of death was lower for dd AC-P than AC-P (HR=0.76; 95% CI 0.61-0.96), and higher for dd AC-P than FEC-D (HR=1.24; 0.99-1.54) and for AC-P than FEC-D (HR=1.61; 1.26-2.06). ER visits / admissions during treatment, were higher for FEC-D (respectively, 50.5% and 23.7%), than AC-P (35.2% and 11.6%) and dd AC-P (30.5% and 8.4%); the differences persisted after PS matching (respectively, 48.2% and 23.5% for FEC-D, 31.1% and 8.7% for dd AC-P; p<0.0001). Risk of HF at 5 years for the PS matched groups was 1.37% for FEC-D and 1.49% for dd AC-P (p=0.71). Conclusions: OS was better for FEC-D and dd AC-P when compared with AC-P. This may be attributable to imbalances in patient characteristics. Propensity score matching for dd AC-P and FEC-D showed no difference in survival or HF risk between the arms but pts treated with FEC-D continued to have more ER visits/admissions.

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Abstract Details

Meeting

2014 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Breast Cancer - Triple-Negative/Cytotoxics/Local Therapy

Track

Breast Cancer

Sub Track

Cytotoxic Chemotherapy

Citation

J Clin Oncol 32:5s, 2014 (suppl; abstr 1081)

DOI

10.1200/jco.2014.32.15_suppl.1081

Abstract #

1081

Poster Bd #

174

Abstract Disclosures