Phase II, Open-label, Single-arm, Multicenter Study to Assess the Activity and Safety of Alectinib as Neoadjuvant Treatment in Surgically Resectable Stage III ALK-positive NSCLC: ALNEO Trial.


Journal

Clinical lung cancer
ISSN: 1938-0690
Titre abrégé: Clin Lung Cancer
Pays: United States
ID NLM: 100893225

Informations de publication

Date de publication:
09 2021
Historique:
received: 06 08 2020
revised: 01 02 2021
accepted: 17 02 2021
pubmed: 26 3 2021
medline: 3 2 2022
entrez: 25 3 2021
Statut: ppublish

Résumé

Alectinib is a potent anaplastic lymphoma kinase (ALK)-tyrosine kinase inhibitor (TKI) which is currently used in the first-line setting of advanced ALK Patients with potentially resectable stage III ALK Our case report supports the feasibility of alectinib as neoadjuvant treatment. ALNEO study will further explore the activity and safety of this novel treatment strategy.

Sections du résumé

BACKGROUND
Alectinib is a potent anaplastic lymphoma kinase (ALK)-tyrosine kinase inhibitor (TKI) which is currently used in the first-line setting of advanced ALK
MATERIALS AND METHODS
Patients with potentially resectable stage III ALK
CONCLUSIONS
Our case report supports the feasibility of alectinib as neoadjuvant treatment. ALNEO study will further explore the activity and safety of this novel treatment strategy.

Identifiants

pubmed: 33762169
pii: S1525-7304(21)00049-8
doi: 10.1016/j.cllc.2021.02.014
pii:
doi:

Substances chimiques

Carbazoles 0
Piperidines 0
Anaplastic Lymphoma Kinase EC 2.7.10.1
alectinib LIJ4CT1Z3Y

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

473-477

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Disclosure M. Tiseo has been on advisory boards and received speakers’ fees for Astra-Zeneca, Pfizer, Eli-Lilly, BMS, Novartis, Roche, MSD, Boehringer Ingelheim, Otsuka, Takeda, and Pierre Fabre. M. Tiseo has received research grants from Astra-Zeneca and Boehringer Ingelheim. A. Leonetti received speakers’ fees for Astra-Zeneca. All other authors declare they have no conflict of interest to disclose.

Auteurs

Alessandro Leonetti (A)

Medical Oncology Unit, University Hospital of Parma, Parma, Italy; Department of Medicine and Surgery, University of Parma, Parma, Italy. Electronic address: aleonetti@ao.pr.it.

Roberta Minari (R)

Medical Oncology Unit, University Hospital of Parma, Parma, Italy.

Luca Boni (L)

Epidemiology Unit, IRCCS San Martino University Hospital, Genova, Italy.

Letizia Gnetti (L)

Pathology Unit, Department of Medicine and Surgery, University Hospital of Parma, Parma, Italy.

Michela Verzè (M)

Medical Oncology Unit, University Hospital of Parma, Parma, Italy.

Luigi Ventura (L)

Thoracic Surgery, Department of Medicine and Surgery, University of Parma, Parma, Italy.

Luca Musini (L)

Thoracic Surgery, Department of Medicine and Surgery, University of Parma, Parma, Italy.

Michele Tognetto (M)

Medical Oncology Unit, University Hospital of Parma, Parma, Italy.

Marcello Tiseo (M)

Medical Oncology Unit, University Hospital of Parma, Parma, Italy; Department of Medicine and Surgery, University of Parma, Parma, Italy.

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Classifications MeSH