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Management of treatment-related adverse events in patients with multiple myeloma
1Haematology Department, University Hospital of Salamanca, Salamanca, Spain. mvmateos@usal.es
Abstract:
The introduction of novel antimyeloma therapies, including thalidomide, lenalidomide and bortezomib, has expanded treatment options for patients with multiple myeloma. These compounds alter the natural history of multiple myeloma and help improve outcomes, but have different and specific toxicity profiles. The major adverse events associated with these treatments are somnolence (thalidomide), venous thromboembolism (thalidomide and lenalidomide), myelosuppression (lenalidomide and bortezomib), gastrointestinal disturbance, and peripheral neuropathy (thalidomide and bortezomib). These adverse events are predictable, consistent, and manageable with patient monitoring, supportive care, and dose reduction and interruption where appropriate. Herein we evaluate the incidence of treatment-related adverse events associated with each of these compounds. We further review the management of these adverse events with a view to delivering optimal therapeutic outcomes in patients with newly diagnosed and relapsed and/or refractory multiple myeloma.
Insights
Novel antimyeloma drugs like thalidomide, lenalidomide, and bortezomib improve outcomes but have specific toxicities. Effective management strategies are crucial for optimizing patient care in multiple myeloma.
Area of Science:
- Hematology
- Oncology
- Pharmacology
Background:
- Novel antimyeloma therapies have transformed multiple myeloma treatment.
- These agents, including thalidomide, lenalidomide, and bortezomib, offer improved outcomes.
- Each therapy possesses a distinct toxicity profile requiring careful management.
Purpose of the Study:
- To evaluate the incidence of treatment-related adverse events for thalidomide, lenalidomide, and bortezomib.
- To review the management strategies for these adverse events.
- To ensure optimal therapeutic outcomes in multiple myeloma patients.
Main Methods:
- Review of incidence data for adverse events associated with novel antimyeloma drugs.
- Evaluation of management approaches for common toxicities.
- Analysis of patient monitoring and supportive care protocols.
Main Results:
- Key adverse events include somnolence, venous thromboembolism, myelosuppression, gastrointestinal disturbance, and peripheral neuropathy.
- Adverse events are predictable and manageable through monitoring, supportive care, and dose adjustments.
- Specific toxicities are linked to individual agents: somnolence (thalidomide), VTE (thalidomide, lenalidomide), myelosuppression (lenalidomide, bortezomib), and neuropathy (thalidomide, bortezomib).
Conclusions:
- Novel antimyeloma therapies offer significant benefits but require vigilant management of their specific adverse events.
- Proactive monitoring and tailored supportive care are essential for mitigating toxicities.
- Effective management of adverse events is key to achieving optimal therapeutic outcomes in multiple myeloma.
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