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Updated: Feb 8, 2026

In Silico Clinical Trials for Cardiovascular Disease
Published on: May 27, 2022
Cardiovascular medications and treatment outcomes in multiple myeloma: insights from phase III clinical trials
Ahmad Y Abuhelwa1,2, Sara A Almansour3, Humaid O Al-Shamsi4,5,6,7
1College of Pharmacy, University of Sharjah, Sharjah, UAE. Ahmad.Abuhelwa@sharjah.ac.ae.
Insights
Patients with multiple myeloma (MM) using ACE inhibitors/ARBs may see improved progression-free survival but face increased adverse events. Other cardiovascular drugs showed no significant impact on MM treatment outcomes.
Area of Science:
- Cardiology
- Hematology
- Oncology
Background:
- Multiple myeloma (MM) patients have a high risk of cardiovascular diseases.
- Cardiovascular medications are frequently used by MM patients.
- Understanding the impact of these medications on MM treatment is crucial.
Purpose of the Study:
- To investigate the association of baseline cardiovascular drug use with survival and adverse events in MM patients.
- To analyze data from Phase III trials (CASTOR, MAIA, POLLUX) of daratumumab, lenalidomide, or bortezomib combinations.
- To assess the impact of specific cardiovascular drug classes on MM treatment outcomes.
Main Methods:
- Retrospective analysis of Phase III clinical trial data.
- Cox proportional hazard analysis for survival outcomes.
- Logistic regression for adverse events (grade ≥3).
- Focus on beta-blockers, calcium channel blockers, ACE inhibitors (ACEI), angiotensin II receptor blockers (ARBs), diuretics, and statins.
Main Results:
- Among 1804 patients, ACEI/ARBs were most common (31%).
- ACEI/ARBs use was linked to better progression-free survival (aHR=0.84) but higher odds of grade ≥3 adverse events (aOR=1.45).
- Diuretic use was also associated with increased odds of grade ≥3 adverse events (aOR=1.53).
- Other cardiovascular drugs showed no significant associations with MM outcomes.
Conclusions:
- ACE inhibitors/ARBs may offer a progression-free survival benefit in MM patients but warrant caution due to increased safety concerns.
- Diuretics are also associated with a higher risk of severe adverse events.
- Baseline use of other common cardiovascular medications does not appear to significantly affect MM treatment outcomes.
- Further research is needed to clarify the complex interplay between cardiovascular drugs and MM treatment.
Abstract:
Patients with multiple myeloma (MM) often use cardiovascular medications due to their increased risk of cardiovascular diseases. This study investigated the associations of baseline use of these drugs with survival and adverse events in MM patients initiating daratumumab, lenalidomide, or bortezomib combination treatments. Data from Phase III trials (CASTOR, MAIA, and POLLUX) were analysed, focusing on beta-blockers, calcium channel blockers, ACE inhibitors (ACEI), angiotensin II receptor blockers (ARBs), diuretics, and statins. Cox proportional hazard analysis and logistic regression were used to assess associations with survival and grade ≥ 3 adverse events. Among 1804 patients, ACEI/ARBs were most common (31%), followed by beta-blockers (23%), statins (21%), calcium channel blockers (17%), and diuretics (16%). ACEI/ARBs was associated with better progression-free survival (adjusted hazard ratio (aHR) [95% CI] = 0.84 [0.71-0.99], P = 0.034) but also higher odds of grade ≥ 3 adverse events (adjusted odds ratio (aOR) = 1.45 [1.06-1.97], P = 0.019). Diuretics were similarly associated with grade ≥ 3 adverse events (aOR = 1.53 [1.01-2.34], P = 0.047). Other cardiovascular drugs showed no significant associations. While ACEI/ARBs may improve progression-free survival, they pose safety concerns. It is reassuring that other cardiovascular drugs were not significantly associated with MM treatment outcomes. Further research is essential to fully understand the implications of these medications.
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