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
323P - SPEN: Unraveling breast cancer's genetic symphony — Prognostic significance and therapeutic insights
Presenter: Sameer Emeish
Session: Poster session 14
324P - Application of advanced machine learning techniques to improve prognosis in primary breast angiosarcoma
Presenter: Haya Kamal
Session: Poster session 14
Resources:
Abstract
325P - The clinical validity of histological grade in neoadjuvant treated breast cancer
Presenter: Sanna Steen
Session: Poster session 14
326P - Exploratory analysis of the association of systemic inflammation and breast cancer recurrence in the Optitrain randomised controlled trial
Presenter: Marlene Rietz
Session: Poster session 14
327P - Monitoring over time of pathological complete response to neoadjuvant chemotherapy in breast cancer patients through an ensemble vision transformers-based model
Presenter: Maria Colomba Comes
Session: Poster session 14
328P - Real-world evidence (RWE) of effectiveness and safety of TCHP regimen: INSIGHT-HER2BC trial interim results
Presenter: Daur Meretukov
Session: Poster session 14
329P - RANK/RANKL, ERBB-2: A putative dual targeting strategy in RANK+/Her2+ breast carcinomas patients
Presenter: Michalis Karamouzis
Session: Poster session 14
330P - Randomized phase II study of neoadjuvant chemotherapy with denosumab compared to chemotherapy alone in hormonal receptor-positive, HER2-negative premenopausal breast cancer patients
Presenter: Shereef Elsamany Mohammed
Session: Poster session 14
331P - Neoadjuvant intetamab in combination with standard chemotherapy for locally advanced HER2-positive breast cancer
Presenter: Mingxia Jiang
Session: Poster session 14
332P - Efficacy, safety and exploratory analysis of neoadjuvant tislelizumab plus nab-paclitaxel followed by epirubicin/cyclophosphamide for TNBC: A phase II TREND trial
Presenter: yingying Xu
Session: Poster session 14