Liquid Biopsy for Advanced NSCLC: A Consensus Statement From the International Association for the Study of Lung Cancer.


Journal

Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
ISSN: 1556-1380
Titre abrégé: J Thorac Oncol
Pays: United States
ID NLM: 101274235

Informations de publication

Date de publication:
10 2021
Historique:
received: 28 02 2021
revised: 03 06 2021
accepted: 21 06 2021
pubmed: 12 7 2021
medline: 25 2 2023
entrez: 11 7 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 34246791
pii: S1556-0864(21)02284-X
doi: 10.1016/j.jtho.2021.06.017
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1647-1662

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Auteurs

Christian Rolfo (C)

Center for Thoracic Oncology, The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York.

Philip Mack (P)

Center for Thoracic Oncology, The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York.

Giorgio V Scagliotti (GV)

Department of Oncology, University of Turin, San Luigi Hospital, Orbassano, Italy.

Charu Aggarwal (C)

Division of Hematology and Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Maria E Arcila (ME)

Department of Pathology, Molecular Diagnostics Service, Memorial Sloan Kettering Cancer Center, New York, New York.

Fabrice Barlesi (F)

CRCM, CNRS, INSERM, Aix Marseille University, Marseille, France; Department of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.

Trever Bivona (T)

Department of Medicine, University of California San Francisco, San Francisco, California; Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, California; Department of Cellular and Molecular Pharmacology, University of California San Francisco, San Francisco, California.

Maximilian Diehn (M)

Department of Radiation Oncology, Stanford Cancer Institute, Stanford University School of Medicine, Stanford, California; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, California.

Caroline Dive (C)

Cancer Research UK Manchester Institute Cancer Biomarker Centre, University of Manchester, Manchester, United Kingdom; Cancer Research UK Lung Cancer Centre of Excellence, University of Manchester, Manchester, United Kingdom.

Rafal Dziadziuszko (R)

Department of Oncology and Radiotherapy, Medical University of Gdańsk, Gdańsk, Poland.

Natasha Leighl (N)

Princess Margaret Hospital, University of Toronto, Toronto, Ontario, Canada.

Umberto Malapelle (U)

Department of Public Health, University Federico II of Naples, Naples, Italy.

Tony Mok (T)

State Key Laboratory of Translational Oncology, Chinese University of Hong Kong, Hong Kong.

Nir Peled (N)

The Legacy Heritage Oncology Center and Dr. Larry Norton Institute, Soroka University Medical Center, Beer-Sheva, Israel.

Luis E Raez (LE)

Thoracic Oncology Program, Memorial Cancer Institute/Memorial Health Care System, Florida International University, Miami, Florida.

Lecia Sequist (L)

Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts; Department of Biostatistics, Massachusetts General Hospital, Boston, Massachusetts; Center for Cancer Research, Massachusetts General Hospital, Boston, Massachusetts.

Lynette Sholl (L)

Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.

Charles Swanton (C)

Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London, United Kingdom; Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, United Kingdom.

Chris Abbosh (C)

Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, United Kingdom.

Daniel Tan (D)

Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore; Duke-NUS Medical School, National University of Singapore, Singapore, Singapore.

Heather Wakelee (H)

Stanford Cancer Institute, Stanford University School of Medicine, Stanford, California.

Ignacio Wistuba (I)

Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Rebecca Bunn (R)

International Association for the Study of Lung Cancer, Aurora, Colorado.

Janet Freeman-Daily (J)

The ROS1ders, Inc., Mountain View, California.

Murry Wynes (M)

Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Chandra Belani (C)

Department of Medicine Penn State College of Medicine, Penn State Cancer Institute, Hershey, Pennsylvania.

Tetsuya Mitsudomi (T)

Division of Thoracic Surgery, Department of Surgery, Kindai University Faculty of Medicine, Ohno-Higashi, Osaka-Sayama, Japan.

David Gandara (D)

Division of Hematology/Oncology, UC Davis Comprehensive Cancer Center, Sacramento, California. Electronic address: drgandara@ucdavis.edu.

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