Clinical staging accuracy and the use of neoadjuvant chemoradiotherapy for cT3N0 rectal cancer: Propensity score matched National Cancer Database analysis.


Journal

American journal of surgery
ISSN: 1879-1883
Titre abrégé: Am J Surg
Pays: United States
ID NLM: 0370473

Informations de publication

Date de publication:
03 2021
Historique:
received: 15 07 2020
revised: 10 11 2020
accepted: 12 11 2020
pubmed: 24 11 2020
medline: 7 4 2021
entrez: 23 11 2020
Statut: ppublish

Résumé

While neoadjuvant chemoradiation therapy (nCRT) is accepted as standard of care for locally advanced rectal cancer, the approach to treatment of patients with clinically staged T3N0 disease has been increasingly debated. This study examines the accuracy of clinical staging for cT3N0 rectal cancer as recorded in the National Cancer Data Base and evaluates the role of nCRT in treating these patients. Total of 15,843 patients with clinically staged T3N0M0 rectal cancer who either received nCRT or proceeded to surgery-first met inclusion criteria. Propensity score matching was employed to balance the groups. 23% of cT3N0 patients undergoing surgery-first were found to have pathologically positive nodes. Another 16% turned out to have < stage II disease on surgical pathology. Survival curves for matched nCRT and surgery-first groups demonstrated a survival advantage for cT3N0 patients treated with nCRT. Poor clinical staging accuracy can result in both undertreatment and overtreatment of cT3N0 rectal cancer.

Sections du résumé

BACKGROUND
While neoadjuvant chemoradiation therapy (nCRT) is accepted as standard of care for locally advanced rectal cancer, the approach to treatment of patients with clinically staged T3N0 disease has been increasingly debated. This study examines the accuracy of clinical staging for cT3N0 rectal cancer as recorded in the National Cancer Data Base and evaluates the role of nCRT in treating these patients.
METHODS
Total of 15,843 patients with clinically staged T3N0M0 rectal cancer who either received nCRT or proceeded to surgery-first met inclusion criteria. Propensity score matching was employed to balance the groups.
RESULTS
23% of cT3N0 patients undergoing surgery-first were found to have pathologically positive nodes. Another 16% turned out to have < stage II disease on surgical pathology. Survival curves for matched nCRT and surgery-first groups demonstrated a survival advantage for cT3N0 patients treated with nCRT.
CONCLUSIONS
Poor clinical staging accuracy can result in both undertreatment and overtreatment of cT3N0 rectal cancer.

Identifiants

pubmed: 33223074
pii: S0002-9610(20)30753-4
doi: 10.1016/j.amjsurg.2020.11.030
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

561-565

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest This work received no outside funding. The authors have no conflicts of interest and no disclosures relevant to the research presented herein.

Auteurs

Dominykas Burneikis (D)

Digestive Disease & Surgery Institute, Cleveland Clinic, United States. Electronic address: burneid@ccf.org.

Olga Lavryk (O)

Digestive Disease & Surgery Institute, Cleveland Clinic, United States.

Emre Gorgun (E)

Digestive Disease & Surgery Institute, Cleveland Clinic, United States.

David Liska (D)

Digestive Disease & Surgery Institute, Cleveland Clinic, United States.

Michael Valente (M)

Digestive Disease & Surgery Institute, Cleveland Clinic, United States.

Bradford Sklow (B)

Digestive Disease & Surgery Institute, Cleveland Clinic, United States.

Matthew Kalady (M)

Department of Surgery, The Ohio State University Wexner Medical Center, Columbus, OH, USA.

Scott R Steele (SR)

Digestive Disease & Surgery Institute, Cleveland Clinic, United States.

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