Natural History and Factors Associated with Overall Survival in Stage IV ALK-Rearranged Non-Small Cell Lung Cancer.


Journal

Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
ISSN: 1556-1380
Titre abrégé: J Thorac Oncol
Pays: United States
ID NLM: 101274235

Informations de publication

Date de publication:
04 2019
Historique:
received: 29 07 2018
revised: 03 12 2018
accepted: 04 12 2018
pubmed: 2 1 2019
medline: 28 4 2020
entrez: 2 1 2019
Statut: ppublish

Résumé

Clinical variables describing the natural history and longitudinal therapy outcomes of stage IV anaplastic lymphoma kinase gene rearrangement positive (ALK-positive) NSCLC and their relationship with long-term overall survival (OS) have not previously been described in detail. Patients with stage IV NSCLC treated with an ALK inhibitor at the University of Colorado Cancer Center from 2009 through November 2017 were identified retrospectively. OS curves were constructed by using Kaplan-Meier methods. Multivariate Cox proportional hazard analysis was used to determine the relationship of variables with OS. Of the 110 patients with ALK-positive NSCLC who were identified, 105 received crizotinib as their initial ALK inhibitor. With a median follow-up time of 47 months, the median OS time from diagnosis of stage IV disease was 81 months (6.8 years). Brain metastases at diagnosis of stage IV disease (hazard ratio = 1.01, p = 0.971) and year of stage IV presentation (p = 0.887) did not influence OS. More organs with tumor at diagnosis of stage IV disease was associated with worse OS (HR = 1.49 for each additional organ with disease, including the CNS [p = 0.002]). Each additional month of pemetrexed-based therapy was associated with a 7% relative decrease in risk of death. Patients with stage IV ALK-positive NSCLC can have prolonged OS. Brain metastases at diagnosis of stage IV disease does not influence OS. Having more organs involved with tumor at stage IV presentation is associated with worse outcomes. Prolonged benefit from pemetrexed is associated with better outcomes.

Identifiants

pubmed: 30599201
pii: S1556-0864(18)33533-0
doi: 10.1016/j.jtho.2018.12.014
pmc: PMC7310567
mid: NIHMS1596062
pii:
doi:

Substances chimiques

Crizotinib 53AH36668S
ALK protein, human EC 2.7.10.1
Anaplastic Lymphoma Kinase EC 2.7.10.1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

691-700

Subventions

Organisme : NCI NIH HHS
ID : P30 CA046934
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA058187
Pays : United States

Informations de copyright

Copyright © 2018 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.

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Auteurs

Jose M Pacheco (JM)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado. Electronic address: jose.m.pacheco@ucdenver.edu.

Dexiang Gao (D)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado; School of Medicine and Colorado School of Public Health, University of Colorado Denver, Anschutz Medical Campus, Aurora, Colorado.

Derek Smith (D)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado; School of Medicine and Colorado School of Public Health, University of Colorado Denver, Anschutz Medical Campus, Aurora, Colorado.

Thomas Purcell (T)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado.

Mark Hancock (M)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado.

Paul Bunn (P)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado.

Tyler Robin (T)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado.

Arthur Liu (A)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado.

Sana Karam (S)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado.

Laurie Gaspar (L)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado.

Brian Kavanagh (B)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado.

Chad Rusthoven (C)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado.

Dara Aisner (D)

Department of Pathology, University of Colorado School of Medicine, Aurora, Colorado.

Robert Doebele (R)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado.

D Ross Camidge (DR)

University of Colorado Cancer Center, Anschutz Medical Campus, Aurora, Colorado.

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Classifications MeSH