Redefining the Risk of Surgery for Clinical Stage IIIA (N2) Non-Small Cell Lung Cancer: A Pooled Analysis of the STS GTSD and ESTS Registry.


Journal

Lung
ISSN: 1432-1750
Titre abrégé: Lung
Pays: United States
ID NLM: 7701875

Informations de publication

Date de publication:
06 2021
Historique:
received: 12 01 2021
accepted: 07 04 2021
pubmed: 29 4 2021
medline: 24 12 2021
entrez: 28 4 2021
Statut: ppublish

Résumé

Management of clinical stage IIIA-N2 (cIIIA-N2) non-small cell lung cancer (NSCLC) remains controversial. We evaluated treatment strategies and outcomes in cIIIA-N2 NSCLC patients who underwent pulmonary resection in The Society of Thoracic Surgeons General Thoracic Surgery Database (STS GTSD) and the European Society of Thoracic Surgeons (ESTS) Registry. The STS GTSD and ESTS Registry were queried for patients who underwent pulmonary resection for cIIIA-N2 NSCLC between 2012 and 2016. Demographic variables, treatment strategies, and outcome measures were collected and analyzed. Significance of differences was determined using the χ Pulmonary resection was performed in 4279 cIIIA-N2 NSCLC patients (2928 STS GTSD; 1351 ESTS). Induction therapy was administered to 49%. Lobectomy was performed in 67.1% and pneumonectomy in 13%. Lobectomy was associated with 19.2% major morbidity and 1.6% operative mortality, while pneumonectomy was associated with 34.1% and 5%, respectively. Induction therapy was associated with a higher rate of major morbidity or mortality than upfront surgery (23.2% vs 19.5%, p = 0.004), driven by pneumonectomy (40.7% vs 30.3%, p = 0.012) rather than lobectomy (20.3% vs 18.8%, p = 0.31). Pulmonary resection for cIIIA-N2 NSCLC is associated with low rates of operative morbidity and mortality, with lobectomy having lower morbidity and mortality than pneumonectomy. Induction therapy, particularly chemoradiotherapy, is associated with a higher rate of composite morbidity or mortality than upfront surgery in pneumonectomy patients but not lobectomy patients.

Sections du résumé

BACKGROUND
Management of clinical stage IIIA-N2 (cIIIA-N2) non-small cell lung cancer (NSCLC) remains controversial. We evaluated treatment strategies and outcomes in cIIIA-N2 NSCLC patients who underwent pulmonary resection in The Society of Thoracic Surgeons General Thoracic Surgery Database (STS GTSD) and the European Society of Thoracic Surgeons (ESTS) Registry.
METHODS
The STS GTSD and ESTS Registry were queried for patients who underwent pulmonary resection for cIIIA-N2 NSCLC between 2012 and 2016. Demographic variables, treatment strategies, and outcome measures were collected and analyzed. Significance of differences was determined using the χ
RESULTS
Pulmonary resection was performed in 4279 cIIIA-N2 NSCLC patients (2928 STS GTSD; 1351 ESTS). Induction therapy was administered to 49%. Lobectomy was performed in 67.1% and pneumonectomy in 13%. Lobectomy was associated with 19.2% major morbidity and 1.6% operative mortality, while pneumonectomy was associated with 34.1% and 5%, respectively. Induction therapy was associated with a higher rate of major morbidity or mortality than upfront surgery (23.2% vs 19.5%, p = 0.004), driven by pneumonectomy (40.7% vs 30.3%, p = 0.012) rather than lobectomy (20.3% vs 18.8%, p = 0.31).
CONCLUSIONS
Pulmonary resection for cIIIA-N2 NSCLC is associated with low rates of operative morbidity and mortality, with lobectomy having lower morbidity and mortality than pneumonectomy. Induction therapy, particularly chemoradiotherapy, is associated with a higher rate of composite morbidity or mortality than upfront surgery in pneumonectomy patients but not lobectomy patients.

Identifiants

pubmed: 33909135
doi: 10.1007/s00408-021-00447-5
pii: 10.1007/s00408-021-00447-5
doi:

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

311-318

Références

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Auteurs

Andrew T Arndt (AT)

Department of Cardiovascular and Thoracic Surgery, Rush University Medical Center, Professional Building, Suite 774, Chicago, IL, 60612, USA. Andrew_T_Arndt@rush.edu.

Alessandro Brunelli (A)

Department of Thoracic Surgery, St. James's University Hospital, Leeds, UK.

Silvia Cicconi (S)

Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.

Pierre-Emmanuel Falcoz (PE)

Department of Thoracic Surgery, Nouvel Hopital Civil, Strasbourg, France.

Michele Salati (M)

Unit of Thoracic Surgery, AOU Ospedali Riuniti, Ancona, Italy.

Benjamin Kozower (B)

Division of Cardiothoracic Surgery, Washington University School of Medicine, St. Louis, MO, USA.

Michael J Liptay (MJ)

Department of Cardiovascular and Thoracic Surgery, Rush University Medical Center, Chicago, IL, 60612, USA.

Gaetano Rocco (G)

Thoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Justin M Karush (JM)

Department of Cardiovascular and Thoracic Surgery, Rush University Medical Center, Chicago, IL, 60612, USA.

Nicole Geissen (N)

Department of Cardiovascular and Thoracic Surgery, Rush University Medical Center, Chicago, IL, 60612, USA.

Sanjib Basu (S)

Department of Cardiovascular and Thoracic Surgery, Rush University Medical Center, Chicago, IL, 60612, USA.

Christopher W Seder (CW)

Department of Cardiovascular and Thoracic Surgery, Rush University Medical Center, Chicago, IL, 60612, USA.

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