Can normalized carcinoembryonic antigen following neoadjuvant chemoradiation predict tumour recurrence after curative resection for locally advanced rectal cancer?


Journal

Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland
ISSN: 1463-1318
Titre abrégé: Colorectal Dis
Pays: England
ID NLM: 100883611

Informations de publication

Date de publication:
06 2021
Historique:
revised: 02 02 2021
received: 22 08 2020
accepted: 04 02 2021
pubmed: 12 2 2021
medline: 4 9 2021
entrez: 11 2 2021
Statut: ppublish

Résumé

The aim of this work was to evaluate whether normalized carcinoembryonic antigen (CEA) following neoadjuvant chemoradiation predicts the prognosis following curative resection in locally advanced rectal cancer. Patients who underwent neoadjuvant chemoradiation and curative resection for locally advanced rectal cancer between 2010 and 2015 were divided into three groups: Group A (n = 119, normal-to-normal): normal CEA before and after neoadjuvant chemoradiation; Group B (n = 37, high-to-normal): elevated CEA before and normal CEA after neoadjuvant chemoradiation; Group C (n = 36, high-to-high): elevated CEA before and after neoadjuvant chemoradiation. Overall and disease-free survival were compared. Univariate and multivariate analyses identified potential predictors for recurrence. One hundred and ninety two patients [median age 59 years (range 31-87), 65.1% male] were identified: 54.7% had low rectal cancer: 12.5% were clinical stage T4 and 70.3% were clinically node positive; 21.9% achieved complete pathological response; 24.5% had abdominoperineal resection (APR); and 70.3% underwent adjuvant chemotherapy following curative resection. Significantly more patients in Group C underwent APR (p = 0.0209), had advanced pathological T stage (P = 0.0065) and a higher prevalence of perineural invasion (p = 0.0042). Overall and disease-free survival were significantly higher for Group A than for Group C [hazard ratio (HR) = 4.32, 95% CI = 1.66-11.21, p = 0.0026 and HR=2.68, 95% CI = 1.33-5.40, p = 0.0057, respectively]. No significant difference was noted between Groups A and B for overall (p = 0.0591) or disease-free (p = 0.2834) survival. Another risk factor associated with recurrence and death was clinical T4 stage; nodal positivity was a risk factor only for recurrence. Elevated CEA after neoadjuvant chemoradiation and clinical stage T4 disease were unfavourable predictors for overall and disease-free survival. Normalized CEA during neoadjuvant chemoradiation may serve as a prognosticator, although pretreatment CEA may significantly affect survival.

Identifiants

pubmed: 33570756
doi: 10.1111/codi.15583
doi:

Substances chimiques

Carcinoembryonic Antigen 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1346-1356

Informations de copyright

© 2021 The Association of Coloproctology of Great Britain and Ireland.

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Auteurs

Youngki Hong (Y)

Department of Colorectal Surgery, Cleveland Clinic Florida, Weston, FL, USA.

Amandeep Ghuman (A)

Department of Colorectal Surgery, Cleveland Clinic Florida, Weston, FL, USA.

Keat Seong Poh (KS)

Department of Colorectal Surgery, Cleveland Clinic Florida, Weston, FL, USA.

Dimitri Krizzuk (D)

Department of Colorectal Surgery, Cleveland Clinic Florida, Weston, FL, USA.

Arun Nagarajan (A)

Department of Hematology and Oncology, Cleveland Clinic Florida, Weston, FL, USA.

Sudha Amarnath (S)

Department of Radiation Oncology, Cleveland Clinic, Cleveland, OH, USA.

Juan J Nogueras (JJ)

Department of Colorectal Surgery, Cleveland Clinic Florida, Weston, FL, USA.

Steven D Wexner (SD)

Department of Colorectal Surgery, Cleveland Clinic Florida, Weston, FL, USA.

Giovanna DaSilva (G)

Department of Colorectal Surgery, Cleveland Clinic Florida, Weston, FL, USA.

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