TY - JOUR
T1 - Prognostic and Predictive Biomarkers of Oligometastatic NSCLC
T2 - New Insights and Clinical Applications
AU - Jongbloed, Mandy
AU - Bortolot, Martina
AU - Wee, Leonard
AU - Huijs, Jarno W. J.
AU - Bellezo, Murillo
AU - Vaes, Rianne D. W.
AU - Nana, Frank Aboubakar
AU - Hartemink, Koen J.
AU - De Ruysscher, Dirk K. M.
AU - Hendriks, Lizza E. L.
PY - 2024/12/1
Y1 - 2024/12/1
N2 - This review discusses the current data on predictive and prognostic biomarkers in oligometastatic NSCLC and discusses whether biomarkers identified in other stages and widespread metastatic disease can be extrapolated to the oligometastatic disease (OMD) setting. Research is underway to explore the prognostic and predictive value of biological attributes of tumor tissue, circulating cells, the tumor microenvironment, and imaging findings as biomarkers of oligometastatic NSCLC. Biomarkers that help define true OMD and predict outcomes are needed for patient selection for oligometastatic treatment, and to avoid futile treatments in patients that will not benefit from locoregional treatment. Nevertheless, these biomarkers are still in the early stages of development and lack prospective validation in clinical trials. Furthermore, the absence of a clear definition of OMD contributes to a heterogeneous study population in which different types of OMD are mixed and treatment strategies are different. Multiple tissue-based, circulating, and imaging features are promising regarding their prognostic and predictive role in NSCLC, but data is still limited and might be biased owing to the inclusion of heterogeneous patient populations. Larger homogeneous and prospective series are needed to assess the prognostic and predictive role of these biomarkers. As obtaining tissue can be difficult and is invasive, the most promising tools for further evaluation are liquid biopsies and imaging-based biomarkers as these can also be used for longitudinal follow-up. (c) 2024 The Authors. Published by Elsevier Inc. on behalf of the International Association for the Study of Lung Cancer. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
AB - This review discusses the current data on predictive and prognostic biomarkers in oligometastatic NSCLC and discusses whether biomarkers identified in other stages and widespread metastatic disease can be extrapolated to the oligometastatic disease (OMD) setting. Research is underway to explore the prognostic and predictive value of biological attributes of tumor tissue, circulating cells, the tumor microenvironment, and imaging findings as biomarkers of oligometastatic NSCLC. Biomarkers that help define true OMD and predict outcomes are needed for patient selection for oligometastatic treatment, and to avoid futile treatments in patients that will not benefit from locoregional treatment. Nevertheless, these biomarkers are still in the early stages of development and lack prospective validation in clinical trials. Furthermore, the absence of a clear definition of OMD contributes to a heterogeneous study population in which different types of OMD are mixed and treatment strategies are different. Multiple tissue-based, circulating, and imaging features are promising regarding their prognostic and predictive role in NSCLC, but data is still limited and might be biased owing to the inclusion of heterogeneous patient populations. Larger homogeneous and prospective series are needed to assess the prognostic and predictive role of these biomarkers. As obtaining tissue can be difficult and is invasive, the most promising tools for further evaluation are liquid biopsies and imaging-based biomarkers as these can also be used for longitudinal follow-up. (c) 2024 The Authors. Published by Elsevier Inc. on behalf of the International Association for the Study of Lung Cancer. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
KW - NSCLC
KW - Oligometastatic disease
KW - Biomarkers
KW - Prognostic
KW - Predictive
KW - CELL LUNG-CANCER
KW - CIRCULATING TUMOR DNA
KW - PD-L1 EXPRESSION
KW - INTRATUMOR HETEROGENEITY
KW - PATHOLOGICAL RESPONSE
KW - RISK STRATIFICATION
KW - RADIATION-THERAPY
KW - VOLUME
KW - RADIOTHERAPY
KW - IMMUNE
U2 - 10.1016/j.jtocrr.2024.100740
DO - 10.1016/j.jtocrr.2024.100740
M3 - (Systematic) Review article
SN - 2666-3643
VL - 5
JO - JTO Clinical and Research Reports
JF - JTO Clinical and Research Reports
IS - 12
M1 - 100740
ER -