Guidance for clinicians and patients with non-small cell lung cancer in the time of precision medicine

Major advances in the diagnosis and treatment of non-small cell lung cancer (NSCLC) have resulted in a sharp decline in associated mortality rates, thereby propelling NSCLC to the forefront of precision medicine. Current guidelines recommend upfront comprehensive molecular testing for all known and...

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Main Authors: Liza C. Villaruz, Mark A. Socinski, Jared Weiss
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-02-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2023.1124167/full
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author Liza C. Villaruz
Mark A. Socinski
Jared Weiss
author_facet Liza C. Villaruz
Mark A. Socinski
Jared Weiss
author_sort Liza C. Villaruz
collection DOAJ
description Major advances in the diagnosis and treatment of non-small cell lung cancer (NSCLC) have resulted in a sharp decline in associated mortality rates, thereby propelling NSCLC to the forefront of precision medicine. Current guidelines recommend upfront comprehensive molecular testing for all known and actionable driver alterations/biomarkers (EGFR, ALK, ROS1, BRAF, KRAS, NTRK, MET, RET, HER2 [ERBB2], and PD-L1), especially in advanced disease stages, as they significantly influence response to therapy. In particular, hybrid capture-based next-generation sequencing (HC-NGS) with an RNA fusion panel to detect gene fusions is a veritable requirement at both diagnosis and progression (resistance) of any-stage non-squamous adenocarcinoma NSCLCs. This testing modality ensures selection of the most timely, appropriate, and personalized treatment, maximization of therapeutic efficacy, and prevention of use of suboptimal/contraindicated therapy. As a complement to clinical testing and treatment, patient, family, and caregiver education is also key to early screening and diagnosis, access to care, coping strategies, positive outcomes, and survival. The advent of social media and increased internet access has amplified the volume of educational and support resources, consequently changing the dynamics of patient care. This review provides guidance on integration of comprehensive genomic testing with an RNA fusion panel as a global diagnostic standard for all adenocarcinoma NSCLC disease stages and provides key information on patient and caregiver education and resources.
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spelling doaj.art-19e5db9909304e20b06b352aad7c3c172023-01-31T05:52:42ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2023-02-011310.3389/fonc.2023.11241671124167Guidance for clinicians and patients with non-small cell lung cancer in the time of precision medicineLiza C. Villaruz0Mark A. Socinski1Jared Weiss2Hillman Cancer Center, Department of Medicine, Division of Hematology/Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA, United StatesAdventHealth Cancer Institute, Orlando, FL, United StatesDivision of Oncology, Lineberger Comprehensive Cancer at the University of North Carolina, Chapel Hill, NC, United StatesMajor advances in the diagnosis and treatment of non-small cell lung cancer (NSCLC) have resulted in a sharp decline in associated mortality rates, thereby propelling NSCLC to the forefront of precision medicine. Current guidelines recommend upfront comprehensive molecular testing for all known and actionable driver alterations/biomarkers (EGFR, ALK, ROS1, BRAF, KRAS, NTRK, MET, RET, HER2 [ERBB2], and PD-L1), especially in advanced disease stages, as they significantly influence response to therapy. In particular, hybrid capture-based next-generation sequencing (HC-NGS) with an RNA fusion panel to detect gene fusions is a veritable requirement at both diagnosis and progression (resistance) of any-stage non-squamous adenocarcinoma NSCLCs. This testing modality ensures selection of the most timely, appropriate, and personalized treatment, maximization of therapeutic efficacy, and prevention of use of suboptimal/contraindicated therapy. As a complement to clinical testing and treatment, patient, family, and caregiver education is also key to early screening and diagnosis, access to care, coping strategies, positive outcomes, and survival. The advent of social media and increased internet access has amplified the volume of educational and support resources, consequently changing the dynamics of patient care. This review provides guidance on integration of comprehensive genomic testing with an RNA fusion panel as a global diagnostic standard for all adenocarcinoma NSCLC disease stages and provides key information on patient and caregiver education and resources.https://www.frontiersin.org/articles/10.3389/fonc.2023.1124167/fulltargeted therapynon-small cell lung cancerbiomarker testingpatient educationnext-generation sequencing
spellingShingle Liza C. Villaruz
Mark A. Socinski
Jared Weiss
Guidance for clinicians and patients with non-small cell lung cancer in the time of precision medicine
Frontiers in Oncology
targeted therapy
non-small cell lung cancer
biomarker testing
patient education
next-generation sequencing
title Guidance for clinicians and patients with non-small cell lung cancer in the time of precision medicine
title_full Guidance for clinicians and patients with non-small cell lung cancer in the time of precision medicine
title_fullStr Guidance for clinicians and patients with non-small cell lung cancer in the time of precision medicine
title_full_unstemmed Guidance for clinicians and patients with non-small cell lung cancer in the time of precision medicine
title_short Guidance for clinicians and patients with non-small cell lung cancer in the time of precision medicine
title_sort guidance for clinicians and patients with non small cell lung cancer in the time of precision medicine
topic targeted therapy
non-small cell lung cancer
biomarker testing
patient education
next-generation sequencing
url https://www.frontiersin.org/articles/10.3389/fonc.2023.1124167/full
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