Real-world ALK Testing Trends in Patients With Advanced Non-Small-Cell Lung Cancer in the United States.


Journal

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

Informations de publication

Date de publication:
01 2023
Historique:
received: 26 04 2022
revised: 15 09 2022
accepted: 29 09 2022
pubmed: 15 11 2022
medline: 28 12 2022
entrez: 14 11 2022
Statut: ppublish

Résumé

Patients with non-small-cell lung cancer (NSCLC) whose tumors harbor anaplastic lymphoma kinase (ALK) rearrangements can be treated with ALK tyrosine kinase inhibitors. We assessed real-world ALK biomarker testing and treatment patterns of patients with NSCLC in the United States. Data were extracted from the Flatiron Health electronic health record-derived deidentified database for patients aged ≥18 years with stage IIIB or IV NSCLC and ≥2 clinic visits between January 2011 and December 2019. Among 60,025 eligible patients, tumors from 36,691 (61.1%) patients were tested for ALK rearrangements, and 1042 (2.8%) tested positive (ALK+). From 2011 to 2019, ALK testing rates increased from 33.1% to 73.0%; testing via fluorescence in situ hybridization declined from 68.3% to 32.1% while next-generation sequencing increased from <1% to 52.2%. Although tissue samples were more commonly used than blood (85.1% vs. 13.5% of tests), blood sample testing increased from 0.1% in 2011 to 28.2% in 2019. Median (interquartile range) time from diagnosis of advanced NSCLC to first ALK+ test result was 23 (13-43) days, including laboratory processing time of 9 (6-14) days. For the 24.7% of patients with an ALK+ test result who began treatment before receiving the positive result, chemotherapy was initiated most often overall until 2018 when immuno-oncology agents became most common. Although ALK testing in NSCLC increased over time, testing rates among eligible patients did not reach 100% during the study period. Treatment decisions for some patients with NSCLC may have been made without important, guideline-recommended biomarker data.

Identifiants

pubmed: 36376172
pii: S1525-7304(22)00213-3
doi: 10.1016/j.cllc.2022.09.010
pii:
doi:

Substances chimiques

Anaplastic Lymphoma Kinase EC 2.7.10.1
Protein Kinase Inhibitors 0
ALK protein, human 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

e39-e49

Informations de copyright

Copyright © 2022. Published by Elsevier Inc.

Auteurs

Huamao M Lin (HM)

Takeda Development Center Americas, Inc., Lexington, MA. Electronic address: Mark.Lin@takeda.com.

Yanyu Wu (Y)

Takeda Development Center Americas, Inc., Lexington, MA.

Yu Yin (Y)

Takeda Development Center Americas, Inc., Lexington, MA.

Huifeng Niu (H)

Takeda Development Center Americas, Inc., Lexington, MA.

Eileen A Curran (EA)

Takeda Development Center Americas, Inc., Lexington, MA.

Christine M Lovly (CM)

Department of Medicine, Division of Hematology-Oncology and Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN.

Michael J Humphries (MJ)

Takeda Pharmaceuticals U.S.A., Inc., Lexington, MA.

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Classifications MeSH