Optimal Management of Adverse Events From Copanlisib in the Treatment of Patients With Non-Hodgkin Lymphomas.


Journal

Clinical lymphoma, myeloma & leukemia
ISSN: 2152-2669
Titre abrégé: Clin Lymphoma Myeloma Leuk
Pays: United States
ID NLM: 101525386

Informations de publication

Date de publication:
03 2019
Historique:
received: 11 10 2018
accepted: 22 11 2018
pubmed: 26 12 2018
medline: 4 6 2020
entrez: 26 12 2018
Statut: ppublish

Résumé

Copanlisib is a phosphoinositol 3-kinase (PI3K) inhibitor approved for the third-line treatment of follicular non-Hodgkin lymphoma. Although the drug is generally well-tolerated, it can be associated with several unique and potentially serious adverse effects (AEs). Two of the most common toxicities not seen with other PI3K inhibitors include hyperglycemia and hypertension, which primarily occur during infusion and resolve shortly thereafter, and likely relate to targeting the PI3K alpha isoform. Other toxicities less commonly observed with copanlisib than with other approved drugs in this class include non-infectious pneumonitis, infections, diarrhea and colitis, and hepatobiliary toxicity. A panel composed of experts in lymphoma, diabetes, and hypertension convened to develop guidance pertaining to the administration of copanlisib and the management of the AEs associated with copanlisib treatment. Recommendations were formulated pertaining to the management of AEs associated with copanlisib treatment, particularly infusion-related hyperglycemia and hypertension, noninfectious pneumonitis, infections, diarrhea, and colitis. The recommendations herein reflect the consensus of the members of this panel, all of whom contributed to these suggested approaches to patient supportive care. There are a number of challenges associated with the use of copanlisib. Infusion-related hypertension and hyperglycemia occur frequently, although they are transient, reversible, and rarely of clinical significance; this report provides guidance as to their management.

Identifiants

pubmed: 30584024
pii: S2152-2650(18)31465-4
doi: 10.1016/j.clml.2018.11.021
pmc: PMC6642803
mid: NIHMS1038643
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Pyrimidines 0
Quinazolines 0
copanlisib WI6V529FZ9

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

135-141

Subventions

Organisme : NCI NIH HHS
ID : K23 CA218897
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

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Auteurs

Bruce D Cheson (BD)

Department of Internal Medicine, Division of Hematology-Oncology, Georgetown Lombardi Comprehensive Cancer Center, Washington, DC. Electronic address: bdc4@georgetown.edu.

Susan O'Brien (S)

Department of Medicine, University of California, Irvine, CA.

Michael S Ewer (MS)

Department of Cardiology, University of Texas MD Anderson Cancer Center, Houston, TX.

Marcus D Goncalves (MD)

Department of Endocrinology, Weill Cornell Medical Center, New York, NY.

Azeez Farooki (A)

Department of Endocrinology, Memorial Sloan Kettering Cancer Center, New York, NY.

Georg Lenz (G)

Department of Hematology, Oncology and Pneumology, Universität Münster, Münster, Germany.

Anthony Yu (A)

Department of Cardiology, Memorial Sloan Kettering Cancer Center, New York, NY.

Richard I Fisher (RI)

Department of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA.

Pierre L Zinzani (PL)

Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.

Martin Dreyling (M)

Department of Internal Medicine, University of Munich, Munich, Germany.

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Classifications MeSH