Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

E-Poster Display

1507P - A retrospective study of angiotensin-converting enzyme inhibitors or beta-blockers to prevent trastuzumab-induced cardiotoxicity

Date

17 Sep 2020

Session

E-Poster Display

Topics

End-of-Life Care;  Immunotherapy

Tumour Site

Presenters

Kai Sun

Citation

Annals of Oncology (2020) 31 (suppl_4): S874-S880. 10.1016/annonc/annonc264

Authors

K. Sun1, K. Anand1, S. Manne2, X. Xu3, M. Niravath3, J.C. Nicolas3, S.L. Jones3, T.A. Patel4, C. Geyer1, J.C. Chang1, P. Niravath1

Author affiliations

  • 1 Medical Oncology, Houston Methodist Cancer Center, 77030 - Houston/US
  • 2 Arthropology, University of California, Berkley, 94720 - California/US
  • 3 Center For Outcomes Research, Houston Methodist Research Institute, 77030 - Houston/US
  • 4 General Oncology, The University of Texas MD Anderson Cancer Center, 77030 - Houston/US

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 1507P

Background

Trastuzumab (TRA) has significantly improved the outcome of HER2+ breast cancer but is associated with a 0.9% to 4% incidence of TRA-induced cardiotoxicity (TIC). Some previous studies investigated using angiotensin-converting enzyme inhibitors (ACEi) and/or beta-blockers (BB) for prevention of TIC but have yielded conflicting results. We examined our data retrospectively to investigate if ACEi or BB may have cardioprotective effects in breast cancer patients receiving TRA.

Methods

We retrospectively queried breast cancer patients who received TRA at our hospital from 5/2016 to 6/2018. Patients demographics, risk factors for TIC (hypertension, diabetes mellitus and hyperlipidemia), chemotherapy, ACEi and BB use, and echocardiograms were recorded and analyzed. TIC is defined as an absolute drop of left ventricular ejection fraction (LVEF) of 16% or more, or 10-15% drop if the resulting LVEF is below the institutional limit of normal. Fisher’s exact test and Mann-Whitney test were used for analysis.

Results

A total of 188 patients with a median age of 55 were retrieved. 68.6% were Caucasian, 19.1% African American, 6.4% Asian, and 5.9% other/unknown. 7/188 (3.7%) subjects developed TIC. 0/26 patient taking concurrent ACEi developed TIC, compared to 4.5% in patients not taking ACEi (p=0.596). However, this was not statistically significant, likely due to a relatively small sample size. Body mass index, risk factors, concurrent BB use and prior anthracycline exposure between groups were also not significantly different (Table). Table: 1507P

Demographics of patients with versus without TIC

Patients with no TIC Patients with TIC P value
Total number 181 7
Body Mass Index 26.8 (23.8-31.0) 24.2 (22.9-35.0) 0.624
Anthracycline exposure 15 (8.3%) 0 (0%) 1.000
Hypertension 35 (19.3%) 1 (14.3%) 1.000
Hyperlipidemia 13 (7.2%) 1 (14.3%) 0.424
Diabetes mellitus 11 (6.1%) 0 (0%) 1.000
ACEi 26 (14.4%) 0 (0%) 0.596
BB 62 (34.3%) 3 (42.8%) 0.694

Conclusions

In our retrospective study, none of the patients receiving TRA and concurrent ACEi developed TIC, as compared to 4.5% developing TIC in those who were not taking ACEi. Our data suggests that ACEi may be cardioprotective in breast cancer patients receiving TRA. However, larger prospective studies are needed to clarify the potential benefit of ACEi.

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.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.