The Relative Survival Impact of Guideline-Concordant Clinical Staging and Stage-Appropriate Treatment of Potentially Curable Non-Small Cell Lung Cancer.


Journal

Chest
ISSN: 1931-3543
Titre abrégé: Chest
Pays: United States
ID NLM: 0231335

Informations de publication

Date de publication:
07 2022
Historique:
received: 27 08 2021
revised: 11 01 2022
accepted: 18 01 2022
pubmed: 6 2 2022
medline: 14 7 2022
entrez: 5 2 2022
Statut: ppublish

Résumé

Lung cancer management guidelines strive to improve outcomes. Theoretically, thorough staging promotes optimal treatment selection. We examined the association between guideline-concordant invasive mediastinal nodal staging, guideline-concordant treatment, and non-small cell lung cancer survival. What is the current practice of invasive mediastinal nodal staging for patients with lung cancer in a structured multidisciplinary care environment? Is guideline-concordant staging associated with guideline-concordant treatment? How do they relate to survival? We evaluated patients with nonmetastatic non-small cell lung cancer diagnosed from 2014 through 2019 in the Multidisciplinary Thoracic Oncology Program of the Baptist Cancer Center, Memphis, Tennessee. We examined patterns of mediastinal nodal staging and stage-stratified treatment, grouping patients into cohorts with guideline-concordant staging alone, guideline-concordant treatment alone, both, or neither. We evaluated overall survival with Kaplan-Meier curves and Cox proportional hazards models. Of 882 patients, 456 (52%) received any invasive mediastinal staging. Seventy-four percent received guideline-concordant staging; guideline-discordant staging decreased from 34% in 2014 to 18% in 2019 (P < .0001). Recipients of guideline-concordant staging were more likely to receive guideline-concordant treatment (83% vs 66%; P < .0001). Sixty-one percent received both guideline-concordant invasive mediastinal staging and guideline-concordant treatment; 13% received guideline-concordant staging alone; 17% received guideline-concordant treatment alone; and 9% received neither. Survival was greatest in patients who received both (adjusted hazard ratio [aHR], 0.41; 95% CI, 0.26-0.63), followed by those who received guideline-concordant treatment alone (aHR, 0.60; 95% CI, 0.36-0.99), and those who received guideline-concordant staging alone (aHR, 0.64; 95% CI, 0.37-1.09) compared with neither (P < .0001, log-rank test). Levels of guideline-concordant staging were high, were rising, and were associated with guideline-concordant treatment selection in this multidisciplinary care cohort. Guideline-concordant staging and guideline-concordant treatment were complementary in their association with improved survival, supporting the connection between these two processes and lung cancer outcomes.

Sections du résumé

BACKGROUND
Lung cancer management guidelines strive to improve outcomes. Theoretically, thorough staging promotes optimal treatment selection. We examined the association between guideline-concordant invasive mediastinal nodal staging, guideline-concordant treatment, and non-small cell lung cancer survival.
RESEARCH QUESTION
What is the current practice of invasive mediastinal nodal staging for patients with lung cancer in a structured multidisciplinary care environment? Is guideline-concordant staging associated with guideline-concordant treatment? How do they relate to survival?
STUDY DESIGN AND METHODS
We evaluated patients with nonmetastatic non-small cell lung cancer diagnosed from 2014 through 2019 in the Multidisciplinary Thoracic Oncology Program of the Baptist Cancer Center, Memphis, Tennessee. We examined patterns of mediastinal nodal staging and stage-stratified treatment, grouping patients into cohorts with guideline-concordant staging alone, guideline-concordant treatment alone, both, or neither. We evaluated overall survival with Kaplan-Meier curves and Cox proportional hazards models.
RESULTS
Of 882 patients, 456 (52%) received any invasive mediastinal staging. Seventy-four percent received guideline-concordant staging; guideline-discordant staging decreased from 34% in 2014 to 18% in 2019 (P < .0001). Recipients of guideline-concordant staging were more likely to receive guideline-concordant treatment (83% vs 66%; P < .0001). Sixty-one percent received both guideline-concordant invasive mediastinal staging and guideline-concordant treatment; 13% received guideline-concordant staging alone; 17% received guideline-concordant treatment alone; and 9% received neither. Survival was greatest in patients who received both (adjusted hazard ratio [aHR], 0.41; 95% CI, 0.26-0.63), followed by those who received guideline-concordant treatment alone (aHR, 0.60; 95% CI, 0.36-0.99), and those who received guideline-concordant staging alone (aHR, 0.64; 95% CI, 0.37-1.09) compared with neither (P < .0001, log-rank test).
INTERPRETATION
Levels of guideline-concordant staging were high, were rising, and were associated with guideline-concordant treatment selection in this multidisciplinary care cohort. Guideline-concordant staging and guideline-concordant treatment were complementary in their association with improved survival, supporting the connection between these two processes and lung cancer outcomes.

Identifiants

pubmed: 35122751
pii: S0012-3692(22)00213-6
doi: 10.1016/j.chest.2022.01.046
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

242-255

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 American College of Chest Physicians. Published by Elsevier Inc. All rights reserved.

Auteurs

Meghan B Meadows-Taylor (MB)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN.

Nicholas R Faris (NR)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN.

Matthew P Smeltzer (MP)

Division of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, University of Memphis, Memphis, TN.

Meredith A Ray (MA)

Division of Epidemiology, Biostatistics, and Environmental Health, School of Public Health, University of Memphis, Memphis, TN.

Carrie Fehnel (C)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN.

Olawale Akinbobola (O)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN.

Folabi Ariganjoye (F)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN.

Anita Patel (A)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN.

Alicia Pacheco (A)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN.

Anurag Mehrotra (A)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN.

Roy Fox (R)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN; Mid-South Pulmonary Specialists, Memphis, TN.

Robert Optican (R)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN; Mid-South Imaging and Therapeutics, Memphis, TN.

Keith Tonkin (K)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN; Mid-South Imaging and Therapeutics, Memphis, TN.

James Machin (J)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN; Mid-South Imaging and Therapeutics, Memphis, TN.

Jeffrey Wright (J)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN; Memphis Lung Physicians, Memphis, TN.

Edward T Robbins (ET)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN.

Raymond U Osarogiagbon (RU)

Multidisciplinary Thoracic Oncology Program, Baptist Cancer Center, Memphis, TN. Electronic address: rosarogi@bmhcc.org.

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