Abstract 308P
Background
The C19 pandemic profoundly impacted access to care and practice patterns. We examine the impact of C19 on treatment modality selection and time to treatment initiation (TTI) among patients with early-stage BC.
Methods
Patients with clinical stage I-III BC diagnosed 2018-2021 were identified in the National Cancer Database (NCDB). Patients were categorized based on year of diagnosis as pre-C19 (2018-2019), early-C19 (2020), and late-C19 (2021). We compared TTI based on first treatment modality (surgery, chemotherapy, radiation, or endocrine therapy) using Wilcoxon rank sum test and implemented logistic regression models to evaluate factors associated with TTI delays >60 days (OR, 95%CI).
Results
We included 567,942 patients. There was a 7.6% decrease in number of BC cases in NCDB from pre- to early-C19, with 8.2% fewer cases of stage I diagnosed in 2020. There were otherwise no major differences in the proportion of diagnosed cases based on age, race, or subtype. The use of neoadjuvant endocrine therapy increased from 4.2% pre-C19 to 7.7% in early-C19. Fewer patients underwent surgery as first treatment (82.4%, 77.1%, and 75.4% in pre-, early-, and late-C19, respectively). Among patients undergoing surgery as initial treatment, the median time to surgery increased from 34 days in pre-and early-C19 to 41 days in late-C19. The proportion of patients experiencing delays in TTI (any modality) was 14.7%, 13.6%, and 19.5% in pre-, early- and late-C19 periods, respectively. In multivariable analysis, the late-C19 period was associated with significant increased risk of delays in treatment initiation (OR 1.39, 95% CI 1.37-1.42) compared to pre-C19. Factors associated with increased risk of delayed treatment initiation included Black race, Hispanic ethnicity, comorbidities, public insurance, or no insurance.
Conclusions
There was a small decrease in BC cases in NCDB during the early-C19 pandemic, with proportionally less stage I cases. There was a change in the initial treatment of choice and an increase in treatment delays, particularly during late-C19, likely due to the impact of the pandemic on the healthcare system. Patients belonging to vulnerable groups were more likely to experience delays in treatment initiation.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Breast Cancer Research Foundation (BCRF-23-190); Susan G. Komen (SAC150061).
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
334P - Cardiovascular events related to CDK4/6 inhibitors: A systematic review and safety meta-analysis of randomized controlled trials
Presenter: Louis Boismoreau
Session: Poster session 14
335P - First-in-human phase I/IIa clinical trial of ZV0203, a novel pertuzumab-based antibody-drug conjugate (ADC), in patients (pts) with Her2 positive advanced solid tumors
Presenter: Fengjuan Lin
Session: Poster session 14
336P - Determination of the most common hereditary mutations associated with breast cancer and ovarian cancer in the population of Ukrainian women
Presenter: Dmytro Nehrulia
Session: Poster session 14
337P - Is presence of molecular residual disease after pathologic complete response associated with relapse in inflammatory breast cancer?
Presenter: Jennifer Chen
Session: Poster session 14
338TiP - EORTC-2129-BCG: Elacestrant for treating ER+/HER2- breast cancer patients with ctDNA relapse (TREAT ctDNA)
Presenter: Michail Ignatiadis
Session: Poster session 14
339TiP - A randomized trial of trastuzumab deruxtecan and biology-driven selection of neoadjuvant treatment for HER2-positive breast cancer (ARIADNE)
Presenter: Theodoros Foukakis
Session: Poster session 14
351P - Abemaciclib plus fulvestrant for HR+, HER2- advanced breast cancer following progression on a prior CDK4/6 inhibitor plus endocrine therapy: Subgroup analyses from the phase III postMONARCH trial
Presenter: Giampaolo Bianchini
Session: Poster session 14
352P - Cost-effectiveness of CDK4/6 inhibitors in first- vs second-line for advanced breast cancer (ABC) in the phase III SONIA trial (BOOG 2017-03)
Presenter: Noor Wortelboer
Session: Poster session 14
353P - Clinical outcomes of treatment with CDK4/6 inhibitors in metastatic breast cancer among carriers of germline pathogenic variants in ATM, BRCA1, BRCA2, CHEK2, and PALB2
Presenter: Robert Scheel
Session: Poster session 14