| Literature DB >> 28466536 |
Jacob P Laubach1, Javid J Moslehi2, Sanjeev A Francis3, Jesús F San Miguel4, Pieter Sonneveld5, Robert Z Orlowski6, Philippe Moreau7, Laura Rosiñol8, Edward A Faber9, Peter Voorhees10, Maria-Victoria Mateos11, Loreta Marquez12, Huaibao Feng12, Avinash Desai13, Helgi van de Velde14, Jennifer Elliott14, Hongliang Shi14, Edward Dow15, Nishith Jobanputra14, Dixie-Lee Esseltine14, Liviu Niculescu14, Kenneth C Anderson1, Sagar Lonial16, Paul G Richardson1.
Abstract
This retrospective analysis aimed to establish the overall cardiac safety profile of bortezomib using patient-level data from one phase 2 and seven phase 3 studies in previously untreated and relapsed/refractory multiple myeloma (MM). Seven clinically relevant primary [congestive heart failure (CHF), arrhythmias, ischaemic heart disease (IHD), cardiac death] and secondary (hypertension, dyspnoea, oedema) cardiac endpoints were defined based on MedDRA v16.0 preferred terms. 2509 bortezomib-treated patients and 1445 patients in non-bortezomib-based control arms were included. The incidence of grade ≥3 CHF was 1·3-4·0% in studies in relapsed/refractory MM and 1·2-4·7% in previously untreated MM (2·0-7·6% all grades), with no significant differences between bortezomib- and non-bortezomib-based arms in comparative studies. Incidences of arrhythmias (1·3-5·9% grade ≥2; 0·6-4·1% grade ≥3), IHD (1·2-2·9% all grades; 0·4-2·7% grade ≥3) and cardiac death (0-1·4%) were low, with no differences between bortezomib-based and non-bortezomib-based arms. Higher rates of oedema (mostly grade 1/2) were seen in bortezomib-based versus non-bortezomib-based arms in one study and a pooled transplant study analysis. Logistic regression analyses of comparative studies showed no impact on cardiac risk with bortezomib-based versus non-bortezomib-based treatment. Bortezomib-based treatment was associated with low incidences of cardiac events.Entities:
Keywords: bortezomib; cardiac; cardio-oncology; multiple myeloma
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Year: 2017 PMID: 28466536 PMCID: PMC6812508 DOI: 10.1111/bjh.14708
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998