TY - JOUR
T1 - Definition of Synchronous Oligometastatic Non–Small Cell Lung Cancer—A Consensus Report
AU - Dingemans, Anne Marie C.
AU - Hendriks, Lizza E.L.
AU - Berghmans, Thierry
AU - Levy, Antonin
AU - Hasan, Baktiar
AU - Faivre-Finn, Corinne
AU - Giaj-Levra, Matteo
AU - Giaj-Levra, Niccolò
AU - Girard, Nicolas
AU - Greillier, Laurent
AU - Lantuéjoul, Sylvie
AU - Edwards, John
AU - O'Brien, Mary
AU - Reck, Martin
AU - Smit, Egbert F.
AU - Van Schil, Paul
AU - Postmus, Pieter E.
AU - Ramella, Sara
AU - Lievens, Yolande
AU - Gaga, Mina
AU - Peled, Nir
AU - Scagliotti, Giorgio V.
AU - Senan, Suresh
AU - Paz-Ares, Luiz
AU - Guckenberger, Matthias
AU - McDonald, Fiona
AU - Ekman, Simon
AU - Cufer, Tanja
AU - Gietema, Hester
AU - Infante, Maurizio
AU - Dziadziuszko, Rafal
AU - Peters, Solange
AU - Porta, Ramon Rami
AU - Vansteenkiste, Johan
AU - Dooms, Christophe
AU - de Ruysscher, Dirk
AU - Besse, Benjamin
AU - Novello, Silvia
N1 - Publisher Copyright:
© 2019 International Association for the Study of Lung Cancer
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Introduction: Improved outcome has been shown in patients with synchronous oligometastatic (sOM) NSCLC when treated with radical intent. As a uniform definition of sOM NSCLC is lacking, we developed a definition and diagnostic criteria by a consensus process. Methods: A pan-European multidisciplinary consensus group was established. Consensus questions were built on the basis of current controversies, and definitions were extracted from a survey, cases and a systematic review. This statement was formulated during a consensus meeting. Results: It was determined that definition of sOM NSCLC is relevant when a radical treatment that may modify the disease course (leading to long-term disease control) is technically feasible for all tumor sites with acceptable toxicity. On the basis of the review, a maximum of five metastases and three organs was proposed. Mediastinal lymph node involvement was not counted as a metastatic site. Fludeoxyglucose F 18 positron emission tomography–computed tomography and brain imaging were considered mandatory. A dedicated liver magnetic resonance imaging scan was advised for a solitary liver metastasis, and thoracoscopy and biopsies of distant ipsilateral pleural sites were recommended for a solitary pleural metastasis. For mediastinal staging, fludeoxyglucose F 18 positron emission tomography–computed tomography was deemed the minimum requirement, with pathological confirmation recommended if this influences the treatment strategy. Biopsy of a solitary metastatic location was mandated unless the multidisciplinary team is of the opinion that the risks outweigh the benefits. Conclusion: A multidisciplinary consensus statement on the definition and staging of sOM NSCLC has been formulated. This statement will help to standardize inclusion criteria in future clinical trials.
AB - Introduction: Improved outcome has been shown in patients with synchronous oligometastatic (sOM) NSCLC when treated with radical intent. As a uniform definition of sOM NSCLC is lacking, we developed a definition and diagnostic criteria by a consensus process. Methods: A pan-European multidisciplinary consensus group was established. Consensus questions were built on the basis of current controversies, and definitions were extracted from a survey, cases and a systematic review. This statement was formulated during a consensus meeting. Results: It was determined that definition of sOM NSCLC is relevant when a radical treatment that may modify the disease course (leading to long-term disease control) is technically feasible for all tumor sites with acceptable toxicity. On the basis of the review, a maximum of five metastases and three organs was proposed. Mediastinal lymph node involvement was not counted as a metastatic site. Fludeoxyglucose F 18 positron emission tomography–computed tomography and brain imaging were considered mandatory. A dedicated liver magnetic resonance imaging scan was advised for a solitary liver metastasis, and thoracoscopy and biopsies of distant ipsilateral pleural sites were recommended for a solitary pleural metastasis. For mediastinal staging, fludeoxyglucose F 18 positron emission tomography–computed tomography was deemed the minimum requirement, with pathological confirmation recommended if this influences the treatment strategy. Biopsy of a solitary metastatic location was mandated unless the multidisciplinary team is of the opinion that the risks outweigh the benefits. Conclusion: A multidisciplinary consensus statement on the definition and staging of sOM NSCLC has been formulated. This statement will help to standardize inclusion criteria in future clinical trials.
KW - Consensus definition
KW - Non–small cell lung cancer
KW - Oligometastatic disease
KW - Staging
UR - http://www.scopus.com/inward/record.url?scp=85074170416&partnerID=8YFLogxK
U2 - 10.1016/j.jtho.2019.07.025
DO - 10.1016/j.jtho.2019.07.025
M3 - Article
C2 - 31398540
AN - SCOPUS:85074170416
SN - 1556-0864
VL - 14
SP - 2109
EP - 2119
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 12
ER -