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Non-Small-Cell Lung Cancer Patients Harboring ROS1 Rearrangement: Real World Testing Practices, Characteristics and Treatment Patterns (ROS1REAL Study)

Authors :
Urska Janzic
Natalie Maimon Rabinovich
Walid Shalata
Waleed Kian
Katarzyna Szymczak
Rafal Dziadziuszko
Marko Jakopovic
Giannis Mountzios
Adam Pluzanski
Antonio Araujo
Andriani Charpidou
Sameh Daher
Abed Agbarya
Source :
Current Oncology, Vol 31, Iss 8, Pp 4369-4381 (2024)
Publication Year :
2024
Publisher :
MDPI AG, 2024.

Abstract

ROS1 rearrangements are considered rare in non-small-cell lung cancer (NSCLC). This retrospective real-world study aimed to evaluate first-line treatment with crizotinib, a tyrosine kinase inhibitor (TKI) standard of care vs. new generation ROS1 anti-cancer agents. Forty-nine ROS1-expressing NSCLC patients, diagnosed with advanced metastatic disease, were included. Molecular profiling using either FISH/CISH or NGS was performed on tissue samples. Twenty-eight patients were treated with crizotinib, while fourteen patients were administered newer drugs (entrectinib, repotrectinib) and seven patients received platinum-doublet chemotherapy in a first-line setting. Overall response rate and disease control rate for the crizotinib and entrectinb/repotrectinib cohort were 68% and 82% vs. 86% and 93%, respectively. Median progression free survival was 1.6 years (95% CI 1.15–2.215) for the crizotinib treatment vs. 2.35 years for the entrectinib/repotrectinib cohort (95% CI 1.19–3.52). Central nervous system progression was noted in 20% and 25% of the crizotinib and entrectinib/repotrectinib cohorts, respectively. This multi-center study presents real-world treatment patterns of ROS1 NSCLC population, indicating that crizotinib exhibited comparable results to entrectinib/repotrectinib in a first-line setting, although both response rate and survival was numerically longer with treatment with newer agents.

Details

Language :
English
ISSN :
17187729 and 11980052
Volume :
31
Issue :
8
Database :
Directory of Open Access Journals
Journal :
Current Oncology
Publication Type :
Academic Journal
Accession number :
edsdoj.b21f604fcc4328811acd70c304e952
Document Type :
article
Full Text :
https://doi.org/10.3390/curroncol31080326