Drug Repositioning in Oncology.


Journal

American journal of therapeutics
ISSN: 1536-3686
Titre abrégé: Am J Ther
Pays: United States
ID NLM: 9441347

Informations de publication

Date de publication:
Historique:
pubmed: 30 4 2019
medline: 30 9 2021
entrez: 30 4 2019
Statut: ppublish

Résumé

The worldwide increase in the occurrence of cancer associated with the limitations of immunotherapy and the emergence of resistance have impaired the prognosis of cancer patients, which leads to the search for alternative treatment methods. Drug repositioning, a well-established process approved by regulatory agencies, is considered an alternative strategy for the fast identification of drugs, because it is relatively less costly and represents lower risks for patients. We report the most relevant studies about drug repositioning in oncology, emphasizing that its implementation faces financial and regulatory obstacles, making the creation of incentives necessary to stimulate the involvement of the pharmaceutical industry. We present 63 studies in which 52 non-anticancer drugs with anticancer activity against a number of malignancies are described. Some have already been the target of phase III studies, such as the Add-Aspirin trial for nonmetastatic solid tumors, as well as 9 other drugs (aprepitant, artesunate, auranofin, captopril, celecoxib, disulfiram, itraconazole, ritonavir, and sertraline) in the CUSP9* clinical trial for the treatment of recurrent glioblastoma. Others have already been successful in repositioning such as thalidomide, zoledronic acid, celecoxib, methotrexate, and gemcitabine. Therefore, drug repositioning represents a promising alternative for the treatment of oncological disorders; however, the support from funding agencies and from the government is still needed, the latter regarding regulatory issues.

Sections du résumé

BACKGROUND BACKGROUND
The worldwide increase in the occurrence of cancer associated with the limitations of immunotherapy and the emergence of resistance have impaired the prognosis of cancer patients, which leads to the search for alternative treatment methods. Drug repositioning, a well-established process approved by regulatory agencies, is considered an alternative strategy for the fast identification of drugs, because it is relatively less costly and represents lower risks for patients.
AREAS OF UNCERTAINTY UNASSIGNED
We report the most relevant studies about drug repositioning in oncology, emphasizing that its implementation faces financial and regulatory obstacles, making the creation of incentives necessary to stimulate the involvement of the pharmaceutical industry.
DATA SOURCES METHODS
We present 63 studies in which 52 non-anticancer drugs with anticancer activity against a number of malignancies are described.
THERAPEUTIC INNOVATIONS UNASSIGNED
Some have already been the target of phase III studies, such as the Add-Aspirin trial for nonmetastatic solid tumors, as well as 9 other drugs (aprepitant, artesunate, auranofin, captopril, celecoxib, disulfiram, itraconazole, ritonavir, and sertraline) in the CUSP9* clinical trial for the treatment of recurrent glioblastoma. Others have already been successful in repositioning such as thalidomide, zoledronic acid, celecoxib, methotrexate, and gemcitabine.
CONCLUSIONS CONCLUSIONS
Therefore, drug repositioning represents a promising alternative for the treatment of oncological disorders; however, the support from funding agencies and from the government is still needed, the latter regarding regulatory issues.

Identifiants

pubmed: 31033488
pii: 00045391-202102000-00009
doi: 10.1097/MJT.0000000000000906
doi:

Substances chimiques

Itraconazole 304NUG5GF4
Ritonavir O3J8G9O825

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e111-e117

Informations de copyright

Copyright © 2019 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to declare.

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Auteurs

Marissa B Serafin (MB)

Universidade Federal de Santa Maria, Programa de Pós-graduacão Em Ciências Farmacêuticas, Santa Maria, RS, Brazil; and.

Angelita Bottega (A)

Universidade Federal de Santa Maria, Programa de Pós-graduacão Em Ciências Farmacêuticas, Santa Maria, RS, Brazil; and.

Taciéli F da Rosa (TF)

Universidade Federal de Santa Maria, Programa de Pós-graduacão Em Ciências Farmacêuticas, Santa Maria, RS, Brazil; and.

Catrine S Machado (CS)

Universidade Federal de Santa Maria, Programa de Pós-graduacão Em Ciências Farmacêuticas, Santa Maria, RS, Brazil; and.

Vitória S Foletto (VS)

Departamento de Análises Clínicas e Toxicológicas, Universidade Federal de Santa Maria, Santa Maria, RS, Brazil.

Silvana S Coelho (SS)

Universidade Federal de Santa Maria, Programa de Pós-graduacão Em Ciências Farmacêuticas, Santa Maria, RS, Brazil; and.

Augusto D da Mota (AD)

Departamento de Análises Clínicas e Toxicológicas, Universidade Federal de Santa Maria, Santa Maria, RS, Brazil.

Rosmari Hörner (R)

Universidade Federal de Santa Maria, Programa de Pós-graduacão Em Ciências Farmacêuticas, Santa Maria, RS, Brazil; and.
Departamento de Análises Clínicas e Toxicológicas, Universidade Federal de Santa Maria, Santa Maria, RS, Brazil.

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