Perioperative therapy in metastatic colorectal cancer: Pattern of use and survival outcomes.


Journal

Journal of surgical oncology
ISSN: 1096-9098
Titre abrégé: J Surg Oncol
Pays: United States
ID NLM: 0222643

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 06 09 2020
revised: 09 10 2020
accepted: 12 10 2020
pubmed: 31 10 2020
medline: 5 3 2021
entrez: 30 10 2020
Statut: ppublish

Résumé

Multimodality therapy of metastatic colorectal cancer (mCRC) is currently considered the standard of care. The aim of this study was to evaluate the impact of perioperative therapy on surgical resection in mCRC. The National Cancer Database was analyzed for affected patients between 2004 and 2013. Univariate and multivariate analyses were done to identify factors associated with patient outcomes. Kaplan-Meier analysis and Cox proportional hazards models were used for the association between patient characteristics and survival. About 61,940 patients with mCRC were identified. Mean age = 63.4 years (SD ± 14). About 69% had a colon primary and 32% had only one metastatic site. Only 49% of those who underwent surgery for both primary and metastatic sites received postoperative chemotherapy (p < .001). Negative prognostic factors included no chemotherapy received (hazard ratio [HR], 2.32; 2.27-2.37; p < .001), more than three metastatic sites (HR, 2.28; 2.09-2.48; p < .001), year of diagnosis between 2004 and 2008 (HR, 1.71; 1.15-1.20; p < .001) and colon tumor location with right worse than left-sided (HR, 1.21; 1.19-1.24; p < .001). Five-year overall survival for resection of the primary and metastatic site (28.2%) was higher than for no surgical treatment (4.7%). Perioperative therapy was associated with improved survival, following resection of metastatic sites or primary tumor.

Sections du résumé

BACKGROUND BACKGROUND
Multimodality therapy of metastatic colorectal cancer (mCRC) is currently considered the standard of care. The aim of this study was to evaluate the impact of perioperative therapy on surgical resection in mCRC.
METHODS METHODS
The National Cancer Database was analyzed for affected patients between 2004 and 2013. Univariate and multivariate analyses were done to identify factors associated with patient outcomes. Kaplan-Meier analysis and Cox proportional hazards models were used for the association between patient characteristics and survival.
RESULTS RESULTS
About 61,940 patients with mCRC were identified. Mean age = 63.4 years (SD ± 14). About 69% had a colon primary and 32% had only one metastatic site. Only 49% of those who underwent surgery for both primary and metastatic sites received postoperative chemotherapy (p < .001). Negative prognostic factors included no chemotherapy received (hazard ratio [HR], 2.32; 2.27-2.37; p < .001), more than three metastatic sites (HR, 2.28; 2.09-2.48; p < .001), year of diagnosis between 2004 and 2008 (HR, 1.71; 1.15-1.20; p < .001) and colon tumor location with right worse than left-sided (HR, 1.21; 1.19-1.24; p < .001). Five-year overall survival for resection of the primary and metastatic site (28.2%) was higher than for no surgical treatment (4.7%).
CONCLUSION CONCLUSIONS
Perioperative therapy was associated with improved survival, following resection of metastatic sites or primary tumor.

Identifiants

pubmed: 33125756
doi: 10.1002/jso.26278
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

596-605

Informations de copyright

© 2020 Wiley Periodicals LLC.

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Auteurs

Olatunji B Alese (OB)

Department of Hematology and Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.

Katerina Zakka (K)

Department of Hematology and Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.

Xingyue Huo (X)

Winship Research Informatics, Emory University, Atlanta, Georgia, USA.

Renjian Jiang (R)

Winship Research Informatics, Emory University, Atlanta, Georgia, USA.

Walid L Shaib (WL)

Department of Hematology and Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.

Mehmet Akce (M)

Department of Hematology and Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.

Madhusmita Behera (M)

Department of Hematology and Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.
Winship Research Informatics, Emory University, Atlanta, Georgia, USA.

Patrick Sullivan (P)

Division of General and GI Surgery, Department of Surgery, Emory University School of Medicine, Atlanta, Georgia, USA.

Christina Wu (C)

Department of Hematology and Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.

Bassel F El-Rayes (BF)

Department of Hematology and Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.

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