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@ARTICLE{Leypoldt:302808,
author = {L. B. Leypoldt and L. Guo and B. Besemer and M. Hänel and
M.-S. Raab and C. Mann and C. S. Michel and H. C.
Reinhardt$^*$ and I. W. Blau and M. Görner and Y.-D. Ko and
M. de Wit and H. Salwender and C. Scheid and U. Graeven and
R. Peceny and P. Staib and A. Dieing and H. Goldschmidt and
C. Bokemeyer and T. Zeller and D. Westermann and K. C.
Weisel and R. Twerenbold and A. Beitzen-Heineke},
title = {{C}ardiac biomarkers for risk stratification in newly
diagnosed high-risk multiple myeloma in the {GMMG}-{CONCEPT}
trial.},
journal = {Cardio-Oncology},
volume = {11},
number = {1},
issn = {2057-3804},
address = {[London]},
publisher = {BioMed Central},
reportid = {DKFZ-2025-01348},
pages = {63},
year = {2025},
abstract = {Cardiovascular adverse events (CVAE) are clinically
relevant side effects during treatment with the proteasome
inhibitor carfilzomib. We investigated the predictive value
of cardiac biomarkers for onset of CVAE in patients with
newly diagnosed high-risk multiple myeloma treated with
isatuximab, carfilzomib, lenalidomide, and dexamethasone in
the GMMG-CONCEPT study (NCT03104842). Patients included in
this prospective, multicenter correlative study were
eligible if a serum sample before treatment initiation and
at ≥ 1 later study time point were available. N-terminal
pro-b-type natriuretic peptide (NT-proBNP) and
high-sensitive Troponin I (hsTropI) were measured using
immunoassays. Time-to-event analyses were performed using
Kaplan-Meier estimators and log-rank test was used for
statistical analysis. Among 126 patients included in this
study, 40 reported incident CVAE. No significant differences
were observed for age, sex, cardiovascular risk factors and
cardiovascular comorbidities between patients who
experienced CVAE compared to patients without CVAE.
NT-proBNP levels were elevated at baseline in 96 $(76\%)$
patients. Neither baseline levels nor change in NT-proBNP
level during early induction cycles were predictive for the
occurrence of CVAE. In contrast, elevation of hsTropI above
the 99th percentile was rare. Patients with hsTropI level
≥ 2.9 ng/L, corresponding to the lower limit of
quantification, showed a higher risk for CVAE compared to
patients with hsTropI < 2.9 ng/L at baseline (p = 0.0023).
In conclusion, in patients with newly diagnosed high-risk
multiple myeloma undergoing carfilzomib-based quadruplet
treatment, low hsTropI pretreatment levels are of high
negative predictive value for the occurrence of CVAE whereas
elevated NT-proBNP levels are very common before treatment
initiation.},
cin = {ED01},
ddc = {610},
cid = {I:(DE-He78)ED01-20160331},
pnm = {899 - ohne Topic (POF4-899)},
pid = {G:(DE-HGF)POF4-899},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40611354},
pmc = {pmc:PMC12224601},
doi = {10.1186/s40959-025-00358-x},
url = {https://inrepo02.dkfz.de/record/302808},
}