Background The novel proteasome inhibitor carfilzomib alone or in combination with other agents is already one of the standard therapies for relapsed and/or refractory multiple myeloma (MM) patients and produces impressive response rates in newly diagnosed MM as well. However, carfilzomib-related cardiovascular adverse events (CVAEs) - including hypertension (all grades: 12.2%; grade >= 3: 4.3%), heart failure (all grades: 4.1%; grade >= 3: 2.5%) and ischemic heart disease (all grades: 1.8%; grade >= 3: 0.8%) - may lead to treatment suspensions. At present, there are neither prospective studies nor expert consensus on the prevention, monitoring and treatment of CVAEs in myeloma patients treated with carfilzomib. Methods An expert panel of the European Myeloma Network in collaboration with the Italian Society of Arterial Hypertension and with the endorsement of the European Hematology Association aimed to provide recommendations to support health professionals in selecting the best management strategies for patients, considering the impact on outcome and the risk-benefit ratio of diagnostic and therapeutic tools, thereby achieving myeloma response with novel combination approaches whilst preventing CVAEs. Results Patients scheduled to receive carfilzomib need a careful cardiovascular evaluation before treatment and an accurate follow-up during treatment. Conclusions A detailed clinical assessment before starting carfilzomib treatment is essential to identify patients at risk for CVAEs, and accurate monitoring of blood pressure and of early signs and symptoms suggestive of cardiac dysfunction remains pivotal to safely administer carfilzomib without treatment interruptions or dose reductions.

Prevention, monitoring and treatment of cardiovascular adverse events in myeloma patients receiving carfilzomib A consensus paper by the European Myeloma Network and the Italian Society of Arterial Hypertension

Bringhen S.
First
;
Milan A.;D'Agostino M.;Gay F.;Larocca A.;Boccadoro M.;
2019-01-01

Abstract

Background The novel proteasome inhibitor carfilzomib alone or in combination with other agents is already one of the standard therapies for relapsed and/or refractory multiple myeloma (MM) patients and produces impressive response rates in newly diagnosed MM as well. However, carfilzomib-related cardiovascular adverse events (CVAEs) - including hypertension (all grades: 12.2%; grade >= 3: 4.3%), heart failure (all grades: 4.1%; grade >= 3: 2.5%) and ischemic heart disease (all grades: 1.8%; grade >= 3: 0.8%) - may lead to treatment suspensions. At present, there are neither prospective studies nor expert consensus on the prevention, monitoring and treatment of CVAEs in myeloma patients treated with carfilzomib. Methods An expert panel of the European Myeloma Network in collaboration with the Italian Society of Arterial Hypertension and with the endorsement of the European Hematology Association aimed to provide recommendations to support health professionals in selecting the best management strategies for patients, considering the impact on outcome and the risk-benefit ratio of diagnostic and therapeutic tools, thereby achieving myeloma response with novel combination approaches whilst preventing CVAEs. Results Patients scheduled to receive carfilzomib need a careful cardiovascular evaluation before treatment and an accurate follow-up during treatment. Conclusions A detailed clinical assessment before starting carfilzomib treatment is essential to identify patients at risk for CVAEs, and accurate monitoring of blood pressure and of early signs and symptoms suggestive of cardiac dysfunction remains pivotal to safely administer carfilzomib without treatment interruptions or dose reductions.
2019
286
1
63
74
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2796
https://onlinelibrary.wiley.com/doi/abs/10.1111/joim.12882
adverse events; blood pressure monitoring; cardiovascular toxicity; carfilzomib; clinical assessment; multiple myeloma
Bringhen S.; Milan A.; D'Agostino M.; Ferri C.; Wasch R.; Gay F.; Larocca A.; Offidani M.; Zweegman S.; Terpos E.; Goldschmidt H.; Cavo M.; Ludwig H.; Driessen C.; Auner H.W.; Caers J.; Gramatzki M.; Dimopoulos M.A.; Boccadoro M.; Einsele H.; Sonneveld P.; Engelhardt M.
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Descrizione: [Author Vsn] Bringhen et al. J Intern Med. 2019 Jul;286(1):63-74. doi: 10.1111/joim.12882. Epub 2019 Apr 8. PMID: 30725503. © 2019 The Association for the Publication of the Journal of Internal Medicine. The publisher's version is available at: https://onlinelibrary.wiley.com/doi/10.1111/joim.12882 | https://doi.org/10.1111/joim.12882 . When citing, please refer to the published version.
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Descrizione: [Pre-print vsn.] Bringhen S et al. J Intern Med. 2019 Jul;286(1):63-74. doi: 10.1111/joim.12882. Epub 2019 Apr 8. PMID: 30725503. © 2019 The Association for the Publication of the Journal of Internal Medicine. This is not the final published version. The publisher's version is available at: https://onlinelibrary.wiley.com/doi/10.1111/joim.12882 | https://doi.org/10.1111/joim.12882 . When citing, please refer to the published version.
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Descrizione: [Restricted access - Published Vsn. and Suppl.] Bringhen et al. J Intern Med. 2019 Jul;286(1):63-74. doi: 10.1111/joim.12882. Epub 2019 Apr 8. PMID: 30725503. © 2019 The Association for the Publication of the Journal of Internal Medicine. Available at: https://onlinelibrary.wiley.com/doi/10.1111/joim.12882 | https://doi.org/10.1111/joim.12882
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1704793
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