Cardiotoxicity and Cardiovascular Biomarkers in Patients With Breast Cancer

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Cardiotoxicity and Cardiovascular Biomarkers in Patients With Breast Cancer : Data From the GeparOcto-GBG 84 Trial. / Rüger, Alexandra Maria; Schneeweiss, Andreas; Seiler, Sabine; Tesch, Hans; van Mackelenbergh, Marion; Marmé, Frederik; Lübbe, Kristina; Sinn, Bruno; Karn, Thomas; Stickeler, Elmar; Müller, Volkmar; Schem, Christian; Denkert, Carsten; Fasching, Peter A; Nekljudova, Valentina; Garfias-Macedo, Tania; Hasenfuß, Gerd; Haverkamp, Wilhelm; Loibl, Sibylle; von Haehling, Stephan.

In: J AM HEART ASSOC, Vol. 9, No. 23, 12.2020, p. e018143.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Rüger, AM, Schneeweiss, A, Seiler, S, Tesch, H, van Mackelenbergh, M, Marmé, F, Lübbe, K, Sinn, B, Karn, T, Stickeler, E, Müller, V, Schem, C, Denkert, C, Fasching, PA, Nekljudova, V, Garfias-Macedo, T, Hasenfuß, G, Haverkamp, W, Loibl, S & von Haehling, S 2020, 'Cardiotoxicity and Cardiovascular Biomarkers in Patients With Breast Cancer: Data From the GeparOcto-GBG 84 Trial', J AM HEART ASSOC, vol. 9, no. 23, pp. e018143. https://doi.org/10.1161/JAHA.120.018143

APA

Rüger, A. M., Schneeweiss, A., Seiler, S., Tesch, H., van Mackelenbergh, M., Marmé, F., Lübbe, K., Sinn, B., Karn, T., Stickeler, E., Müller, V., Schem, C., Denkert, C., Fasching, P. A., Nekljudova, V., Garfias-Macedo, T., Hasenfuß, G., Haverkamp, W., Loibl, S., & von Haehling, S. (2020). Cardiotoxicity and Cardiovascular Biomarkers in Patients With Breast Cancer: Data From the GeparOcto-GBG 84 Trial. J AM HEART ASSOC, 9(23), e018143. https://doi.org/10.1161/JAHA.120.018143

Vancouver

Bibtex

@article{889831ea9d464c8895359354b05d30dc,
title = "Cardiotoxicity and Cardiovascular Biomarkers in Patients With Breast Cancer: Data From the GeparOcto-GBG 84 Trial",
abstract = "Background Patients with breast cancer can be affected by cardiotoxic reactions through cancer therapies. Cardiac biomarkers, like NT-proBNP (N-terminal pro-B-type natriuretic peptide) and high-sensitivity cardiac troponin T, might have predictive value. Methods and Results Echocardiography, ECG, hemodynamic parameters, NT-proBNP and high-sensitivity cardiac troponin T were assessed in 853 patients with early-stage breast cancer randomized in the German Breast Group GeparOcto-GBG 84 phase III trial. Patients received neo-adjuvant dose-dense, dose-intensified epirubicin, paclitaxel, and cyclophosphamide (iddEPC group, n=424) or paclitaxel, non-pegylated doxorubicin, and in triple negative breast cancer, (paclitaxel, non-pegylated doxorubicin, carboplatin group, n=429) treatment for 18 weeks. Patients positive for human epidermal growth receptor 2 (n=354, 41.5%) received monoclonal antibodies on top of allocated therapy; 119 (12.9%) of all patients showed a cardiotoxic reaction during therapy (15 [1.8%] using a more strict definition). Presence of cardiotoxic reactions was irrespective of treatment allocation (P=0.31). Small but significant increases in NT-proBNP developed early in patients with a cardiotoxic reaction as compared with those without in whom NT-proBNP rose only towards the end of therapy (P=0.04). High-sensitivity cardiac troponin T rose early in both groups. Logistic regression showed that NT-proBNP (odds ratio [OR], 1.03; 95% CI, 1.008-1.055; P=0.01) and hemoglobin (OR, 1.31; 95% CI, 1.05-1.63; P=0.02) measured at 6 weeks after treatment initiation were significantly associated with cardiotoxic reactions. Conclusions NT-proBNP and hemoglobin are significantly associated with cardiotoxic reactions in patients with early-stage breast cancer undergoing dose-dense and dose-intensified chemotherapy, but high-sensitivity cardiac troponin T is not. Registration URL: http://www.clinicaltrials.gov; Unique identifier: NCT02125344.",
author = "R{\"u}ger, {Alexandra Maria} and Andreas Schneeweiss and Sabine Seiler and Hans Tesch and {van Mackelenbergh}, Marion and Frederik Marm{\'e} and Kristina L{\"u}bbe and Bruno Sinn and Thomas Karn and Elmar Stickeler and Volkmar M{\"u}ller and Christian Schem and Carsten Denkert and Fasching, {Peter A} and Valentina Nekljudova and Tania Garfias-Macedo and Gerd Hasenfu{\ss} and Wilhelm Haverkamp and Sibylle Loibl and {von Haehling}, Stephan",
year = "2020",
month = dec,
doi = "10.1161/JAHA.120.018143",
language = "English",
volume = "9",
pages = "e018143",
journal = "J AM HEART ASSOC",
issn = "2047-9980",
publisher = "Wiley-Blackwell",
number = "23",

}

RIS

TY - JOUR

T1 - Cardiotoxicity and Cardiovascular Biomarkers in Patients With Breast Cancer

T2 - Data From the GeparOcto-GBG 84 Trial

AU - Rüger, Alexandra Maria

AU - Schneeweiss, Andreas

AU - Seiler, Sabine

AU - Tesch, Hans

AU - van Mackelenbergh, Marion

AU - Marmé, Frederik

AU - Lübbe, Kristina

AU - Sinn, Bruno

AU - Karn, Thomas

AU - Stickeler, Elmar

AU - Müller, Volkmar

AU - Schem, Christian

AU - Denkert, Carsten

AU - Fasching, Peter A

AU - Nekljudova, Valentina

AU - Garfias-Macedo, Tania

AU - Hasenfuß, Gerd

AU - Haverkamp, Wilhelm

AU - Loibl, Sibylle

AU - von Haehling, Stephan

PY - 2020/12

Y1 - 2020/12

N2 - Background Patients with breast cancer can be affected by cardiotoxic reactions through cancer therapies. Cardiac biomarkers, like NT-proBNP (N-terminal pro-B-type natriuretic peptide) and high-sensitivity cardiac troponin T, might have predictive value. Methods and Results Echocardiography, ECG, hemodynamic parameters, NT-proBNP and high-sensitivity cardiac troponin T were assessed in 853 patients with early-stage breast cancer randomized in the German Breast Group GeparOcto-GBG 84 phase III trial. Patients received neo-adjuvant dose-dense, dose-intensified epirubicin, paclitaxel, and cyclophosphamide (iddEPC group, n=424) or paclitaxel, non-pegylated doxorubicin, and in triple negative breast cancer, (paclitaxel, non-pegylated doxorubicin, carboplatin group, n=429) treatment for 18 weeks. Patients positive for human epidermal growth receptor 2 (n=354, 41.5%) received monoclonal antibodies on top of allocated therapy; 119 (12.9%) of all patients showed a cardiotoxic reaction during therapy (15 [1.8%] using a more strict definition). Presence of cardiotoxic reactions was irrespective of treatment allocation (P=0.31). Small but significant increases in NT-proBNP developed early in patients with a cardiotoxic reaction as compared with those without in whom NT-proBNP rose only towards the end of therapy (P=0.04). High-sensitivity cardiac troponin T rose early in both groups. Logistic regression showed that NT-proBNP (odds ratio [OR], 1.03; 95% CI, 1.008-1.055; P=0.01) and hemoglobin (OR, 1.31; 95% CI, 1.05-1.63; P=0.02) measured at 6 weeks after treatment initiation were significantly associated with cardiotoxic reactions. Conclusions NT-proBNP and hemoglobin are significantly associated with cardiotoxic reactions in patients with early-stage breast cancer undergoing dose-dense and dose-intensified chemotherapy, but high-sensitivity cardiac troponin T is not. Registration URL: http://www.clinicaltrials.gov; Unique identifier: NCT02125344.

AB - Background Patients with breast cancer can be affected by cardiotoxic reactions through cancer therapies. Cardiac biomarkers, like NT-proBNP (N-terminal pro-B-type natriuretic peptide) and high-sensitivity cardiac troponin T, might have predictive value. Methods and Results Echocardiography, ECG, hemodynamic parameters, NT-proBNP and high-sensitivity cardiac troponin T were assessed in 853 patients with early-stage breast cancer randomized in the German Breast Group GeparOcto-GBG 84 phase III trial. Patients received neo-adjuvant dose-dense, dose-intensified epirubicin, paclitaxel, and cyclophosphamide (iddEPC group, n=424) or paclitaxel, non-pegylated doxorubicin, and in triple negative breast cancer, (paclitaxel, non-pegylated doxorubicin, carboplatin group, n=429) treatment for 18 weeks. Patients positive for human epidermal growth receptor 2 (n=354, 41.5%) received monoclonal antibodies on top of allocated therapy; 119 (12.9%) of all patients showed a cardiotoxic reaction during therapy (15 [1.8%] using a more strict definition). Presence of cardiotoxic reactions was irrespective of treatment allocation (P=0.31). Small but significant increases in NT-proBNP developed early in patients with a cardiotoxic reaction as compared with those without in whom NT-proBNP rose only towards the end of therapy (P=0.04). High-sensitivity cardiac troponin T rose early in both groups. Logistic regression showed that NT-proBNP (odds ratio [OR], 1.03; 95% CI, 1.008-1.055; P=0.01) and hemoglobin (OR, 1.31; 95% CI, 1.05-1.63; P=0.02) measured at 6 weeks after treatment initiation were significantly associated with cardiotoxic reactions. Conclusions NT-proBNP and hemoglobin are significantly associated with cardiotoxic reactions in patients with early-stage breast cancer undergoing dose-dense and dose-intensified chemotherapy, but high-sensitivity cardiac troponin T is not. Registration URL: http://www.clinicaltrials.gov; Unique identifier: NCT02125344.

U2 - 10.1161/JAHA.120.018143

DO - 10.1161/JAHA.120.018143

M3 - SCORING: Journal article

C2 - 33191846

VL - 9

SP - e018143

JO - J AM HEART ASSOC

JF - J AM HEART ASSOC

SN - 2047-9980

IS - 23

ER -