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Monitoring and Management of Toxicities of Novel B Cell Signaling Agents.
Rhodes, Joanna; Mato, Anthony; Sharman, Jeff P.
Affiliation
  • Rhodes J; University of Pennsylvania, 3400 Civic Center Blvd, PCAM 12 South, Philadelphia, PA, 19104, USA. Joanna.rhodes@uphs.upenn.edu.
  • Mato A; Memorial Sloan Kettering Cancer Center, 1275 York Ave, New York, NY, 10065, USA.
  • Sharman JP; Williamette Valley Cancer Institute and Research Center, Eugene, OR, USA.
Curr Oncol Rep ; 20(6): 49, 2018 04 11.
Article in En | MEDLINE | ID: mdl-29644450
ABSTRACT
PURPOSE REVIEW 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. RECENT

FINDINGS:

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.
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Full text: 1 Database: MEDLINE Main subject: Lymphoma, Non-Hodgkin / B-Lymphocytes / Receptors, Antigen, B-Cell / Antineoplastic Agents Limits: Humans Language: En Journal: Curr Oncol Rep Journal subject: NEOPLASIAS Year: 2018 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Lymphoma, Non-Hodgkin / B-Lymphocytes / Receptors, Antigen, B-Cell / Antineoplastic Agents Limits: Humans Language: En Journal: Curr Oncol Rep Journal subject: NEOPLASIAS Year: 2018 Type: Article Affiliation country: United States