ALTA-2: Phase II study of brigatinib in patients with ALK-positive, advanced non-small-cell lung cancer who progressed on alectinib or ceritinib.


Journal

Future oncology (London, England)
ISSN: 1744-8301
Titre abrégé: Future Oncol
Pays: England
ID NLM: 101256629

Informations de publication

Date de publication:
May 2021
Historique:
pubmed: 12 2 2021
medline: 9 11 2021
entrez: 11 2 2021
Statut: ppublish

Résumé

Anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitors (TKIs) have improved outcomes in Lay abstract Tyrosine kinase inhibitor medications (like crizotinib, alectinib or ceritinib) may work as the first treatment for people with non-small-cell lung cancer (NSCLC) that has spread to other parts of the body and has the ALK+ mutation (ALK+ NSCLC) in tumor testing. However, after a while, many people stop responding to treatment with one of these medicines. Brigatinib is a tyrosine kinase inhibitor medicine that may be effective in people with ALK+ NSCLC who have stopped responding to alectinib or ceritinib treatment. We describe the need for and design of a study of brigatinib in people with ALK+ NSCLC whose disease got worse on alectinib or ceritinib.

Autres résumés

Type: plain-language-summary (eng)
Lay abstract Tyrosine kinase inhibitor medications (like crizotinib, alectinib or ceritinib) may work as the first treatment for people with non-small-cell lung cancer (NSCLC) that has spread to other parts of the body and has the ALK+ mutation (ALK+ NSCLC) in tumor testing. However, after a while, many people stop responding to treatment with one of these medicines. Brigatinib is a tyrosine kinase inhibitor medicine that may be effective in people with ALK+ NSCLC who have stopped responding to alectinib or ceritinib treatment. We describe the need for and design of a study of brigatinib in people with ALK+ NSCLC whose disease got worse on alectinib or ceritinib.

Identifiants

pubmed: 33569983
doi: 10.2217/fon-2020-1119
doi:

Substances chimiques

Carbazoles 0
Organophosphorus Compounds 0
Piperidines 0
Protein Kinase Inhibitors 0
Pyrimidines 0
Sulfones 0
ALK protein, human EC 2.7.10.1
Anaplastic Lymphoma Kinase EC 2.7.10.1
brigatinib HYW8DB273J
ceritinib K418KG2GET
alectinib LIJ4CT1Z3Y

Banques de données

ClinicalTrials.gov
['NCT03535740']

Types de publication

Clinical Trial Protocol Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1709-1719

Subventions

Organisme : ARIAD Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited

Auteurs

Edward S Kim (ES)

Levine Cancer Institute, Atrium Health, Charlotte, NC 28210, USA.

Fabrice Barlesi (F)

Multidisciplinary Oncology & Therapeutic Innovations Department, Aix-Marseille University, CNRS, INSERM, CRCM, Marseille, 13007, France.
Gustave Roussy Cancer Campus, Villejuif, 94805, France.

Tony Mok (T)

State Key Laboratory of Translational Oncology, The Chinese University of Hong Kong, Hong Kong, 999077, China.

Myung-Ju Ahn (MJ)

Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, 135-710, South Korea.

Junwu Shen (J)

Millennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Cambridge, MA 02139, USA.

Pingkuan Zhang (P)

Millennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Cambridge, MA 02139, USA.

Sai-Hong Ignatius Ou (SI)

Chao Family Comprehensive Cancer Center, University of California Irvine School of Medicine, Orange, CA 92868, USA.

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Classifications MeSH