TY - JOUR
T1 - Liquid Biopsy for Advanced NSCLC
T2 - A Consensus Statement From the International Association for the Study of Lung Cancer
AU - Rolfo, Christian
AU - Mack, Philip
AU - Scagliotti, Giorgio V.
AU - Aggarwal, Charu
AU - Arcila, Maria E.
AU - Barlesi, Fabrice
AU - Bivona, Trever
AU - Diehn, Maximilian
AU - Dive, Caroline
AU - Dziadziuszko, Rafal
AU - Leighl, Natasha
AU - Malapelle, Umberto
AU - Mok, Tony
AU - Peled, Nir
AU - Raez, Luis E.
AU - Sequist, Lecia
AU - Sholl, Lynette
AU - Swanton, Charles
AU - Abbosh, Chris
AU - Tan, Daniel
AU - Wakelee, Heather
AU - Wistuba, Ignacio
AU - Bunn, Rebecca
AU - Freeman-Daily, Janet
AU - Wynes, Murry
AU - Belani, Chandra
AU - Mitsudomi, Tetsuya
AU - Gandara, David
N1 - Publisher Copyright:
© 2021
PY - 2021/10/1
Y1 - 2021/10/1
N2 - Although precision medicine has had a mixed impact on the clinical management of patients with advanced-stage cancer overall, for NSCLC, and more specifically for lung adenocarcinoma, the advances have been dramatic, largely owing to the genomic complexity and growing number of druggable oncogene drivers. Furthermore, although tumor tissue is historically the “accepted standard” biospecimen for these molecular analyses, there are considerable innate limitations. Thus, liquid biopsy represents a practical alternative source for investigating tumor-derived somatic alterations. Although data are most robust in NSCLC, patients with other cancer types may also benefit from this minimally invasive approach to facilitate selection of targeted therapies. The liquid biopsy approach includes a variety of methodologies for circulating analytes. From a clinical point of view, plasma circulating tumor DNA is the most extensively studied and widely adopted alternative to tissue tumor genotyping in solid tumors, including NSCLC, first entering clinical practice for detection of EGFR mutations in NSCLC. Since the publication of the first International Association for the Study of Lung Cancer (IASLC) liquid biopsy statement in 2018, several additional advances have been made in this field, leading to changes in the therapeutic decision-making algorithm for advanced NSCLC and prompting this 2021 update. In view of the novel and impressive technological advances made in the past few years, the growing clinical application of plasma-based, next-generation sequencing, and the recent Food and Drug and Administration approval in the United States of two different assays for circulating tumor DNA analysis, IASLC revisited the role of liquid biopsy in therapeutic decision-making in a recent workshop in October 2020 and the question of “plasma first” versus “tissue first” approach toward molecular testing for advanced NSCLC. Moreover, evidence-based recommendations from IASLC provide an international perspective on when to order which test and how to interpret the results. Here, we present updates and additional considerations to the previous statement article as a consensus from a multidisciplinary and international team of experts selected by IASLC.
AB - Although precision medicine has had a mixed impact on the clinical management of patients with advanced-stage cancer overall, for NSCLC, and more specifically for lung adenocarcinoma, the advances have been dramatic, largely owing to the genomic complexity and growing number of druggable oncogene drivers. Furthermore, although tumor tissue is historically the “accepted standard” biospecimen for these molecular analyses, there are considerable innate limitations. Thus, liquid biopsy represents a practical alternative source for investigating tumor-derived somatic alterations. Although data are most robust in NSCLC, patients with other cancer types may also benefit from this minimally invasive approach to facilitate selection of targeted therapies. The liquid biopsy approach includes a variety of methodologies for circulating analytes. From a clinical point of view, plasma circulating tumor DNA is the most extensively studied and widely adopted alternative to tissue tumor genotyping in solid tumors, including NSCLC, first entering clinical practice for detection of EGFR mutations in NSCLC. Since the publication of the first International Association for the Study of Lung Cancer (IASLC) liquid biopsy statement in 2018, several additional advances have been made in this field, leading to changes in the therapeutic decision-making algorithm for advanced NSCLC and prompting this 2021 update. In view of the novel and impressive technological advances made in the past few years, the growing clinical application of plasma-based, next-generation sequencing, and the recent Food and Drug and Administration approval in the United States of two different assays for circulating tumor DNA analysis, IASLC revisited the role of liquid biopsy in therapeutic decision-making in a recent workshop in October 2020 and the question of “plasma first” versus “tissue first” approach toward molecular testing for advanced NSCLC. Moreover, evidence-based recommendations from IASLC provide an international perspective on when to order which test and how to interpret the results. Here, we present updates and additional considerations to the previous statement article as a consensus from a multidisciplinary and international team of experts selected by IASLC.
KW - ctDNA
KW - IASLC
KW - Immunotherapy
KW - Liquid biopsy
KW - NSCLC
KW - Oncogene addicted
UR - http://www.scopus.com/inward/record.url?scp=85112439169&partnerID=8YFLogxK
U2 - 10.1016/j.jtho.2021.06.017
DO - 10.1016/j.jtho.2021.06.017
M3 - Review article
C2 - 34246791
AN - SCOPUS:85112439169
SN - 1556-0864
VL - 16
SP - 1647
EP - 1662
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 10
ER -