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Monitoring and Management of Toxicities of Novel B Cell Signaling Agents
- Source :
- Current oncology reports. 20(6)
- Publication Year :
- 2018
-
Abstract
- B cell signaling agents, including ibrutinib, idelalisib, and the BCL-2 inhibitor venetoclax have become an integral part of therapy for patients with non-Hodgkin’s lymphomas. The toxicity profiles of these medications is distinct from chemoimmunotherapy. Here, we will review the mechanism of action of these drugs, their efficacy, and toxicity management. Ibrutinib use is associated with increased risk of atrial fibrillation and bleeding which can be managed using dose interruptions and modifications. Patients on idelalisib require close clinical and frequent laboratory monitoring, particularly of liver function tests to ensure there are no serious adverse events. Monitoring for infections is important in patients on both idelalisib and ibrutinib. Venetoclax requires close clinical and laboratory monitoring to prevent significant tumor lysis. Targeted B cell receptor therapies each have unique side effect profiles which require careful clinical monitoring. As we continue to use these therapies, optimal management strategies will continue to be elucidated.
- Subjects :
- 0301 basic medicine
Oncology
medicine.medical_specialty
Side effect
B-cell receptor
Receptors, Antigen, B-Cell
Antineoplastic Agents
Hemorrhage
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Piperidines
Chemoimmunotherapy
Internal medicine
Atrial Fibrillation
medicine
Humans
Adverse effect
Quinazolinones
B-Lymphocytes
Sulfonamides
medicine.diagnostic_test
Venetoclax
business.industry
Adenine
Lymphoma, Non-Hodgkin
Bridged Bicyclo Compounds, Heterocyclic
030104 developmental biology
Pyrimidines
chemistry
Purines
030220 oncology & carcinogenesis
Ibrutinib
Pyrazoles
Liver function tests
business
Idelalisib
Subjects
Details
- ISSN :
- 15346269
- Volume :
- 20
- Issue :
- 6
- Database :
- OpenAIRE
- Journal :
- Current oncology reports
- Accession number :
- edsair.doi.dedup.....7e93644c77dd008533d213418de07918