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ePoster Display

749P - Cardiotoxicity in patients treated with PARP-inhibitors

Date

16 Sep 2021

Session

ePoster Display

Topics

Management of Systemic Therapy Toxicities;  Supportive Care and Symptom Management

Tumour Site

Presenters

Mariola Blanco Clemente

Citation

Annals of Oncology (2021) 32 (suppl_5): S725-S772. 10.1016/annonc/annonc703

Authors

M. Blanco Clemente1, M. Martinez Cutillas1, Y. Garitaonaindía Díaz1, C.D. Mitroi2, B. Núñez García1, M. Mendez1, J.C. Sánchez González1, B. Cantos Sánchez de Ibargüen1, A. Gonzalez del Alba1, B. Menchen Viso3, M. Provencio Pulla1, C. Maximiano Alonso1

Author affiliations

  • 1 Medical Oncology Department, Hospital Universitario Puerta de Hierro-Majadahonda, 28222 - Majadahonda/ES
  • 2 Cardiology, Hospital Universitario Puerta de Hierro-Majadahonda, 28222 - Majadahonda/ES
  • 3 Pharmacology Department, Hospital Universitario Puerta de Hierro-Majadahonda, 28222 - Majadahonda/ES

Resources

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Abstract 749P

Background

PARP-inhibitors target pathogenic BRCA mutations and homologous recombination deficiency, representing a novel therapeutic approach in patients with this specific alteration, offering longer survival. However, their use in clinical practice has revealed a number of important cardiovascular side effects which can decrease patients' quality of life. This has been little researched, and the information we have is scarce.

Methods

We conducted an observational retropective study selecting patients treated with PARP-inhibitors between 2018 and 2021 in our institution, and analyzed their cardiovascular risk factors (CVRF). The aim of this study was to assess the incidence of cardiovascular events in this population.

Results

A total of 44 patients were analyzed. Data regarding demographic characteristics, CVRF and oncological information are shown in the table. When we analyzed cardiovascular events the results were as follows: the most frequent events were hypertension (20.5%) and palpitations (18.6%), most of them requiring cardiologic assessment and treatment with beta-blockers (16.3%) or antihypertensive drugs. 9.3% of the patients presented an ECG alteration and only 4.6% echocardiographic abnormalities. Two patients required hospital admission, because of an acute coronary síndrome and a pulmonary embolism. There were no congestive heart failure episodes related to PARP-inhibitors treatment. No patient had to stop treatment due to cardiotoxicity and there were no deaths related with cardiological events. 25% of the patients were referred to the cardiologist in order to optimize treatment and continued periodic reviews. Table: 749P

Sex Males: 4.7% Females: 95.3%
Median age 55.0
Hypertension 11.6%
Diabetes 7.0%
Hypercholesterolemia 16.3%
Smoking habit Non-smoker 46.5% Smoker 14.0% Former smoker 39.5%
History of coronary syndrome 4.7%
Valvular disease 2.3%
Arrhythmia 7.0%
Anticoagulant/Antiplatelet treatment 14%
Familiar history of heart disease 4.7%
Type of tumor Ovarian cancer: 93% Prostate cancer: 4.7% Breast cancer: 2.3%
Stage I: 6.9% II: 6.9% III: 53.6% IV: 32.6%
Previous cardiotoxic treatments Cisplatin: 4.7% Anthracyclines: 55.8% Antiangiogenic: 39.5% HER2 targeted therapy: 4.7% Thoracic radiotherapy: 7%
PARP-inhibitor Olaparib: 46.5% Niraparib: 53.5%
Median duration of treatment (months) 10.0 (1.0 - 53.0)
.

Conclusions

Almost half of the patients in our study experienced some kind of cardiac event. Prospective studies with cardiovascular comprehensive follow-up protocols are needed. Due to the increased use of these drugs, it’s important to highlight the role of the cardiologist in order to optimize treatment, improve patients' symptoms and carry out a multidisciplinary approach.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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