Abstract 286P
Background
Although 5-year is recommended for adjuvant endocrine therapy (AET) for breast cancer patients, discontinuation of AET is common. We investigated the effect of early discontinuation to AET on patient survival.
Methods
We identified all female patients diagnosed with non-metastatic primary breast cancer during 2010-2015 who were aged 50 to 80 years with positive estrogen receptor (ER+) and underwent surgery in Alberta, Canada. To account for AET discontinuation due to palliative care, patients experienced recurrence or death within 6-month of AET discontinuation were categorized as AET adherent. Multivariate Cox regression was used to evaluate the effect of AET on survival, adjusting for patient and tumour characteristics including age tumour grade, stage, comorbidity.
Results
A total of 6930 patients were identified with a median age 63 years (IQR: 56-70). 85% of patients had positive progesterone receptor, and 90% were stage I or II. 1391 (20.1%) patients did not get AET, 3669 (52.9%) patients discontinued AET within 5 years (non-adherence), and 1870 (27.0%) patients were AET adherent. In non-adherence group, Tamoxifen, Aromatase Inhibitors (AIs) and both were prescribed to 43%, had, 29.0% and 28.0% patients, respectively. Compared to the no-AET group, both the non-adherence and adherence group had lower hazard ratios (HR) of 0.73 (95%CI: 0.63-0.84) and 0.76 (95%CI: 0.65-0.89) for recurrence-free survival (RFS), respectively, and 0.59 (95%CI: 0.51-0.69) and 0.52 (95%CI: 0.44-0.62) for overall survival (OS), respectively. Multivariate analysis also indicated improved HR in non-adherence group (RFS: 0.56, 95%CI: 0.48-0.66; OS: 0.48, 95%CI: 0.41-0.57) and adherence group (RFS: 0.55, 95%CI: 0.46-0.65; OS: 0.40, 95%CI: 0.33-0.49). Progesterone receptor positive was associated with a lower HR of 0.70 (95%CI: 0.54-0.91) for breast cancer specific survival (BCSS), and comorbidity was associated with higher HR for RFS and OS, but not BCSS.
Conclusions
Adjuvant endocrine therapy (AET) improves survival outcomes in breast cancer patients. Effective efforts to improve adherence to AET are needed.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Breast Tumour Group.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
259P - Relationship between initial tumor burden and the probability of pathological complete response within molecular subtypes of early breast cancer treated with neoadjuvant chemotherapy
Presenter: Nicolas Roussot
Session: Poster session 14
260P - Impact of HER2-low status on clinicopathological characteristics and pathological complete response in luminal and triple-negative early breast cancer
Presenter: Katarzyna Pogoda
Session: Poster session 14
261P - Subtyping of residual disease (RD) following neoadjuvant chemotherapy (NACT) for triple negative breast cancer (TNBC): Evolution and prognostic impact
Presenter: Isabel Echavarria Diaz-Guardamino
Session: Poster session 14
262P - Predictive clinico-biological factors of toxicity associated to neo-adjuvant chemo- immunotherapy in early-stage triple-negative breast cancer
Presenter: Elsa Volant
Session: Poster session 14
263P - Association between clinicopathological characteristics and pathological complete response in patients with triple negative breast cancer treated by neoadjuvant chemo-immunotherapy
Presenter: Clara Helal
Session: Poster session 14
264P - Neuropsychological and morphological effects of simultaneous exercise during neo-/adjuvant chemotherapy in breast cancer patients: The Exercise Cancer and Cognition (ECCO) study
Presenter: David Kiesl
Session: Poster session 14
265P - Association of clinical benefit of adjuvant capecitabine and RCB class in triple negative breast cancer (TNBC) patients with residual disease following neoadjuvant chemotherapy
Presenter: Shinyoung Lee
Session: Poster session 14
266P - Association of RAD51 and efficacy outcomes in patients with HER2-negative breast cancer (BC) and homologous recombination deficiency (HRD): Post-hoc analysis of the GeparOla trial
Presenter: Guillermo Villacampa
Session: Poster session 14
267P - The tumour microenvironment influences long-term tamoxifen treatment response in breast cancer patients
Presenter: Paula Camargo Romera
Session: Poster session 14
268P - Impact of B cell and plasma cell infiltration on survival in early-stage breast cancer (BC) without recurrence
Presenter: Laura Angelats
Session: Poster session 14