Abstract 338P
Background
Breast cancer (BC) survivorship guidelines recommend follow-up (F/U) with a schedule of physician visits and annual mammography. However, literature reflects an increasing reliance on advanced imaging. Our goal was to analyze BC F/U practice with its roots and effects at a population level.
Methods
We included women ≥18 years with early BC undergoing surgery between 2012-2014. We accessed the data warehouse of Lombardy Region in Italy. After calculating the annual frequency of each imaging per patient, we included the derived covariates in unsupervised clustering to set three statistically different groups with increasing F/U intensity, ie minimal, moderate and maximal. We used the Kaplan-Meier method for overall survival (OS) estimates and the Cox model for multivariable analysis.
Results
Overall 28,775 women entered the study, median age was 61 years (IQR 49-72), median time since diagnosis 87.6 months (IQR 77.7-97.9), 69.7% had breast-conservative surgery. Of the 862,955 exams prescribed in the 5 years after surgery, 12.8% were mammograms. Ultrasound (64.7%) was the most common non recommended imaging, followed by computed tomography (11.7%), magnetic resonance (6.2%), and bone scan (4.6%). Intensive F/U was more likely after triple negative (30.1%) and HER2 positive (27.8%) than luminal-like BC (13.1%). Surveillance intensity decreased over time, resulting in 56% of BC survivors having minimal F/U from the third year after surgery onwords. At a 12 month landmark analysis, OS was 80.8%, 87.4% and 66.2% in women having minimal, medium, and maximal intensive F/U. The survival benefit of medium intensive F/U was significant in luminal-like; whereas, the negative effect of maximal intensive F/U extended to all subtypes and was independent of age, surgery, adjuvant and radiotherapy (HR 2.16, 1.99-2.36).
Conclusions
Use of non recommended imaging is common after BC surgery and increases with increasing risk of relapse. Due to the retrospective nature of our study, survival findings are only hypotheses generating. While intensive F/U possibly included women with poor prognostic factors not accounted for by the adjustment, medium intensive F/U might have allowed for timely/curative intervention of recurrent BC. Data overall offers an opportunity to discuss current F/U strategies.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Fondazione IRCCS Istituto Nazionale dei Tumori.
Funding
This study is part of the project “I controlli periodici (follow-up) dopo la diagnosi e le terapie in pazienti liberi da malattia e asintomatici: verso una personalizzazione delle strategie di follow-up” supported by Grant n. RR33 of Lombardy Region, Italy.
Disclosure
S. Di Cosimo: Financial Interests, Personal, Other, Ad hoc project/protocol reviewer: MEDSIR; Financial Interests, Personal, Advisory Board, Treatment of HER2-positive breast cancer: Pier Fabre; Financial Interests, Personal, Other, Medical meeting material setup and distribution; Speaker Bureau: IQVIA. All other authors have declared no conflicts of interest.
Resources from the same session
371P - Adherence to standardized and structured electronic symptom reporting (ePRO) via mobile app in HER2-positive breast cancer treated with HER2 biosimilar trastuzumab
Presenter: Andreas Trojan
Session: Poster session 03
372P - Prevalence of BRCA1 and BRCA2 mutation among Indian breast cancer patients: A multicentre cross-sectional study
Presenter: Shona Nag
Session: Poster session 03
374P - Evaluation of symptom severity, tolerability, and physical function in the I-SPY2 trial
Presenter: Amrita Basu
Session: Poster session 03
375TiP - A phase I, 2-part, multicenter, first-in-human dose-escalation and dose-expansion study of DS-1103a with trastuzumab deruxtecan (T-DXd) in patients with advanced solid tumors
Presenter: Ludimila Cavalcante
Session: Poster session 03
388P - Subgroup analysis of patients (pts) with HER2-low metastatic breast cancer (mBC) with brain metastases (BMs) at baseline from DESTINY-Breast04, a randomized phase III study of trastuzumab deruxtecan (T-DXd) vs treatment of physician’s choice (TPC)
Presenter: Junji Tsurutani
Session: Poster session 03
391P - Detrimental effect on overall survival of CDK4/6 inhibitor dose reduction if immortal time bias is considered
Presenter: Andreas Bjerrum
Session: Poster session 03
392P - The prognostic impact of BMI in patients with HR+/HER2- advanced breast cancer on first-line endocrine therapy with or without a CDK 4/6 inhibitor
Presenter: Senna Lammers
Session: Poster session 03