Validation of a prognostic model including the number of harvested lymph-nodes in the setting of non-small cell lung cancer patients undergoing curative resection: a multicenter analysis.


Journal

Minerva surgery
ISSN: 2724-5438
Titre abrégé: Minerva Surg
Pays: Italy
ID NLM: 101777295

Informations de publication

Date de publication:
Jun 2022
Historique:
pubmed: 3 8 2021
medline: 27 5 2022
entrez: 2 8 2021
Statut: ppublish

Résumé

The prognostic role of the extension of lymphadenectomy in non-small-cell lung cancer is still a debated and intriguing issue. The aim of this study is to validate a prognostic score including the number of resected lymph-nodes previously reported using a large multicenter dataset. From 01/2002 to 12/2012, data on 4858 NSCLC patients undergoing curative-intent surgery in six institutions were retrospectively reviewed. To test the discriminative ability of the model, composed of a panel of high-risk, pathologic stage, nodal status, age, number of Resected Nodes and intermediate risk factors (gender, grading, histology), was determined. The Kaplan-Meier method was used to estimate overall (OS), cancer-specific (CSS) and disease-free survival (DFS) curves, and the log rank test was adopted to evaluate the differences between groups. Pathological stages were: 1) I in 46.5%, II in 24.1%, III in 27.8% and IV in 1.6% of cases. Overall, 5-year OS, CSS and DFS were 54.6%, 76.7% and 44.8%, respectively. Stratifying the sample of 3948 patients with complete data into low-risk (LR, #107), Intermediate-risk (IR, #1268) and High-Risk (HR, #2573) groups, the optimal prognostic discrimination power of this score was confirmed (C-statistics: 0.71, 95%CI 69-73). Specifically in LR, IR and HR, 5-year OS was 83.5%, 66.4% and 46.2% (P<0.0001), 5y-CSS was 95.8%, 89% and 69% (P<0.0001), and 5y-DFS was 74.7%, 59.1% and 35.5% (P<0.0001), respectively. Our study confirms the optimal prognostic discrimination power of the previous prognostic model including the number of harvested nodes.

Sections du résumé

BACKGROUND BACKGROUND
The prognostic role of the extension of lymphadenectomy in non-small-cell lung cancer is still a debated and intriguing issue. The aim of this study is to validate a prognostic score including the number of resected lymph-nodes previously reported using a large multicenter dataset.
METHODS METHODS
From 01/2002 to 12/2012, data on 4858 NSCLC patients undergoing curative-intent surgery in six institutions were retrospectively reviewed. To test the discriminative ability of the model, composed of a panel of high-risk, pathologic stage, nodal status, age, number of Resected Nodes and intermediate risk factors (gender, grading, histology), was determined. The Kaplan-Meier method was used to estimate overall (OS), cancer-specific (CSS) and disease-free survival (DFS) curves, and the log rank test was adopted to evaluate the differences between groups.
RESULTS RESULTS
Pathological stages were: 1) I in 46.5%, II in 24.1%, III in 27.8% and IV in 1.6% of cases. Overall, 5-year OS, CSS and DFS were 54.6%, 76.7% and 44.8%, respectively. Stratifying the sample of 3948 patients with complete data into low-risk (LR, #107), Intermediate-risk (IR, #1268) and High-Risk (HR, #2573) groups, the optimal prognostic discrimination power of this score was confirmed (C-statistics: 0.71, 95%CI 69-73). Specifically in LR, IR and HR, 5-year OS was 83.5%, 66.4% and 46.2% (P<0.0001), 5y-CSS was 95.8%, 89% and 69% (P<0.0001), and 5y-DFS was 74.7%, 59.1% and 35.5% (P<0.0001), respectively.
CONCLUSIONS CONCLUSIONS
Our study confirms the optimal prognostic discrimination power of the previous prognostic model including the number of harvested nodes.

Identifiants

pubmed: 34338459
pii: S2724-5691.21.08902-4
doi: 10.23736/S2724-5691.21.08902-4
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

214-220

Auteurs

Marco Chiappetta (M)

Sacred Heart Catholic University, Rome, Italy - marco.chiappetta@policlinicogemelli.it.
Department of Thoracic Surgery, IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy - marco.chiappetta@policlinicogemelli.it.

Giovanni Leuzzi (G)

Unit Thoracic Surgery, IRCCS Istituto Nazionale Tumori Foundation, Milan, Italy.

Isabella Sperduti (I)

Department of Biostatistics, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Emilio Bria (E)

Sacred Heart Catholic University, Rome, Italy.
Department of Medical Oncology, IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Felice Mucilli (F)

Department of General and Thoracic Surgery, SS. Annunziata University Hospital, Chieti, Italy.

Giovanni B Ratto (GB)

Division of Thoracic Surgery, IRCCS San Martino University Hospital, University of Genoa, Genoa, Italy.

Filippo Lococo (F)

Sacred Heart Catholic University, Rome, Italy.
Department of Thoracic Surgery, IRCCS A. Gemelli University Polyclinic Foundation, Rome, Italy.

Pier L Filosso (PL)

Department of Thoracic Surgery, University of Turin, San Giovanni Battista Hospital, Turin, Italy.

Lorenzo Spaggiari (L)

Division of Thoracic Surgery, European Institute of Oncology, University of Milan, Milan, Italy.

Francesco Facciolo (F)

Department of Thoracic Surgery, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

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