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A retrospective analysis of 3954 patients in phase 2/3 trials of bortezomib for the treatment of multiple myeloma: towards providing a benchmark for the cardiac safety profile of proteasome inhibition in multiple myeloma.
- Laubach, Jacob;
- Moslehi, Javid;
- Francis, Sanjeev;
- San Miguel, Jesús;
- Sonneveld, Pieter;
- Orlowski, Robert;
- Moreau, Philippe;
- Rosiñol, Laura;
- Faber, Edward;
- Voorhees, Peter;
- Mateos, Maria-Victoria;
- Marquez, Loreta;
- Feng, Huaibao;
- Desai, Avinash;
- van de Velde, Helgi;
- Elliott, Jennifer;
- Shi, Hongliang;
- Dow, Edward;
- Jobanputra, Nishith;
- Esseltine, Dixie-Lee;
- Niculescu, Liviu;
- Anderson, Kenneth;
- Lonial, Sagar;
- Richardson, Paul
- et al.
Published Web Location
https://doi.org/10.1111/bjh.14708Abstract
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.
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