Assessment of subtype prevalence and the impact of HER2-directed therapy on emergency department (ED) utilization by real-world breast cancer patients.
Abstract
e24095 Background: Breast cancer is the most common malignant disease in women and subtype is a key prognostic factor. In HER2-positive disease, HER2-directed therapies are the mainstay of treatment, as they have yielded a massive improvement in long-term outcomes. On the downside, these drugs carry the risk of cardiotoxicity. This study aimed to assess reasons for ED presentations in breast cancer patients, highlighting subtype-specific differences in ED presentation and 3-month mortality (3MM) and the occurrence of cardiologic side effects in patients receiving HER2-directed therapy. Methods: This single-centre retrospective study evaluated ED visits of breast cancer patients at an Austrian tertiary care centre. The frequency distribution of the breast cancer subtypes luminal A, luminal B/HER2-negative, luminal B/HER2-positive, HER2-positive (non-luminal) and triple negative were calculated. Subtype-specific 3MM rates were calculated for palliative and curative patients separately with a Chi-Square test. An association between HER2-directed therapies and ED visits due to cardiologic symptoms (decompensated heart failure, cardiomyopathy, arrhythmias [atrial fibrillation, unspecified tachycardia] and hypertensive derailment) was investigated using a Chi Square test and a multinomial logistic regression controlling for age. Results: There was a total of 463 ED visits among 322 patients (curative setting: 94, palliative setting: 228) between 1 st August 2016 and 31 st December 2019. Median age was 62 years with a range of 25-95 years. Subtype distribution was as follows: 39 % (n = 126) luminal B/HER2-negative, 23 % (n = 74) triple negative, 19 % (n = 60) luminal B/HER2-positive, 10 % (n = 32) luminal A and 9 % (n = 30) HER2-positive (non-luminal). Breast cancer subtype was significantly associated with 3MM after ED visits in palliative patients (p = 0.006), with the highest mortality rate observed in triple negative disease (56 %). A total of 68 patients had received HER2-directed therapy before ED visits. Active HER2-directed therapy was significantly associated with a higher rate of cardiologic ED visits (OR = 4.67, 95%CI [1.72; 10.02]). 56 % of these visits resulted in hospitalisation. Conclusions: Breast cancer subtype apparently influenced both the frequency of ED visits and subsequent survival outcomes. HER2-directed therapy significantly increased the risk of cardiologic emergency visits in this cohort of real-world cancer patients. These findings indicate the need for tailored cardio-oncology care strategies to optimize tolerability, improve patients’ quality of life, and reduce healthcare burdens.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (14)
Sandra Mayer
Division of Oncology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria
Anna Pfarrhofer
Division of Oncology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria
Sophie Neubauer
Division of Oncology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria
Sabina Pasalic
Division of Oncology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria
Georg Jeryczynski
Division of Oncology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria
Maximilian Marhold
Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria
Jutta Bergler-Klein
Division of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria
Thorsten Fuereder
Department of Medicine I, Division of Oncology, Medical University of Vienna, Vienna
Filippo Cacioppo
Anton Laggner
Department of Emergency Medicine, Medical University of Vienna, Vienna, Austria
Wilhelm Behringer
Matthias Preusser
Rupert Bartsch
Medical University of Vienna, Department of Medicine 1, Division of Oncology, Vienna, Austria
Christoph Minichsdorfer
Division of Oncology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria