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  3. The IASLC Lung Cancer Staging Project: Proposals for the Revision of the N Descriptors in the Forthcoming 9th Edition of the TNM Classification for Lung Cancer.
 

The IASLC Lung Cancer Staging Project: Proposals for the Revision of the N Descriptors in the Forthcoming 9th Edition of the TNM Classification for Lung Cancer.

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BORIS DOI
10.48350/187366
Date of Publication
May 2024
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
Huang, James
Osarogiagbon, Raymond U
Giroux, Dorothy J
Nishimura, Katherine K
Bille, Andrea
Cardillo, Giuseppe
Detterbeck, Frank
Kernstine, Kemp
Kim, Hong Kwan
Lievens, Yolande
Lim, Eric
Marom, Edith
Prosch, Helmut
Putora, Paul Martin
Universitätsklinik für Radio-Onkologie
Rami-Porta, Ramon
Rice, David
Rocco, Gaetano
Rusch, Valerie W
Opitz, Isabelle
Vasquez, Francisco Suarez
Van Schil, Paul
Jeffrey Yang, Chi-Fu
Asamura, Hisao
Subject(s)

600 - Technology::610...

Series
Journal of thoracic oncology
ISSN or ISBN (if monograph)
1556-1380
Publisher
Elsevier
Language
English
Publisher DOI
10.1016/j.jtho.2023.10.012
PubMed ID
37866624
Uncontrolled Keywords

Lung cancer Lung canc...

Description
INTRODUCTION

The accurate assessment of nodal (N) status is crucial to the management and prognostication of non-metastatic non-small cell lung cancer. We sought to determine whether the current N descriptors should be maintained or revised for the upcoming 9th edition of the international Tumor Node Metastasis (TNM) lung cancer staging system.

METHODS

Data was assembled by the International Association for the Study of Lung Cancer on patients with non-small cell lung cancer, detailing both clinical and pathologic N status, with information about anatomic location and individual station-level identification. Survival was calculated by the Kaplan-Meier method and prognostic groups were assessed by a Cox regression analysis.

RESULTS

Data for clinical N and pathologic N status were available in 45,032 and 35,009 patients, respectively. The current N0 to N3 descriptors for both clinical N and pathologic N categories demonstrated prognostically distinct groups. Furthermore, single station N2 involvement (N2a) demonstrated better prognosis than multistation N2 involvement (N2b) in both clinical and pathologic classifications, and the differences between all neighboring nodal subcategories were highly significant. The prognostic differences between N2a and N2b were robust and consistent across resection status, histologic type, T category, and geographic region.

CONCLUSIONS

The current N descriptors should be maintained, with the addition of new sub-descriptors to N2 for single station involvement (N2a) and multiple station involvement (N2b).
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/170813
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1-s2.0-S1556086423023109-main.pdftextAdobe PDF1.89 MBpublisheracceptedOpen
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