Glucagon-like peptide 1 agonists in cardio-oncology: is it time for a specific focus? - Scorecard - MDSpire

Glucagon-like peptide 1 agonists in cardio-oncology: is it time for a specific focus?

  • By

  • Teresa López-Fernández

  • Pietro Ameri

  • February 8, 2025

  • 0 min

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Clinical Scorecard: Exploring the Role of Glucagon-like Peptide 1 Agonists in Cardio-Oncology: Should We Shift Our Focus?

At a Glance

CategoryDetail
ConditionMultiple myeloma with comorbid Type 2 diabetes mellitus and cardiovascular risk
Key MechanismsGLP1a improve glycaemic control, exert cardioprotective effects via weight reduction, decreased oxidative stress, improved endothelial function, anti-inflammatory actions, and may modulate tumour progression through cAMP, PI3K/Akt, and AMPK pathways
Target PopulationPatients with multiple myeloma and Type 2 diabetes mellitus receiving proteasome inhibitors
Care SettingOncology and cardiology outpatient and inpatient settings managing MM patients with cardiovascular comorbidities

Key Highlights

  • Proteasome inhibitors in MM increase cardiovascular risks including heart failure and ischemic heart disease.
  • GLP1a use in MM patients with T2DM is associated with reduced major adverse cardiovascular events, heart failure, and all-cause mortality.
  • GLP1a may have dual benefits by improving cardiometabolic status and potentially modulating MM tumour progression.

Guideline-Based Recommendations

Diagnosis

  • Assess cardiovascular risk factors and comorbidities including T2DM in patients with multiple myeloma prior to proteasome inhibitor therapy.

Management

  • Consider GLP1a therapy for glycaemic control in MM patients with T2DM to potentially reduce cardiovascular events and mortality.
  • Combine GLP1a therapy with structured lifestyle interventions to optimize cardiometabolic and oncologic outcomes.

Monitoring & Follow-up

  • Monitor cardiovascular status and glycaemic control regularly in MM patients receiving proteasome inhibitors and GLP1a.
  • Observe for gastrointestinal complications, although GLP1a use was not associated with increased risk in the studied cohort.

Risks

  • Be aware of potential cardiovascular risks associated with proteasome inhibitors in MM patients.
  • Recognize that current evidence on GLP1a benefits in MM is observational; further randomized trials are needed.

Patient & Prescribing Data

Adults with multiple myeloma and Type 2 diabetes mellitus receiving proteasome inhibitors

GLP1a use was associated with a 33% lower risk of major adverse cardiovascular events, 43% reduced heart failure risk, and 44% lower all-cause mortality without increased gastrointestinal complications.

Clinical Best Practices

  • Incorporate cardiovascular risk assessment in MM patients before initiating proteasome inhibitors.
  • Use GLP1a as part of a personalized treatment plan for MM patients with T2DM to improve cardiovascular outcomes.
  • Support GLP1a therapy with lifestyle modifications to enhance overall patient health and quality of life.
  • Advocate for randomized controlled trials to validate observational findings and clarify GLP1a’s role in MM management.
  • Consider health economic evaluations to assess long-term cost-effectiveness of GLP1a in this population.

References

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