Contribution of Immunoscore and Molecular Features to Survival Prediction in Stage III Colon Cancer.


Journal

JNCI cancer spectrum
ISSN: 2515-5091
Titre abrégé: JNCI Cancer Spectr
Pays: England
ID NLM: 101721827

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 21 10 2019
revised: 17 01 2020
accepted: 24 03 2020
entrez: 27 5 2020
pubmed: 27 5 2020
medline: 27 5 2020
Statut: epublish

Résumé

The American Joint Committee on Cancer staging and other prognostic tools fail to account for stage-independent variability in outcome. We developed a prognostic classifier adding Immunoscore to clinicopathological and molecular features in patients with stage III colon cancer. Patient (n = 559) data from the FOLFOX arm of adjuvant trial NCCTG N0147 were used to construct Cox models for predicting disease-free survival (DFS). Variables included age, sex, T stage, positive lymph nodes (+LNs), N stage, performance status, histologic grade, sidedness, Poorer DFS was found for tumors that were T4 vs T3 (hazard ratio [HR] = 1.76, 95% confidence interval [CI] = 1.19 to 2.60; The Immunoscore can enhance the accuracy of survival prediction among patients with stage III colon cancer.

Sections du résumé

BACKGROUND BACKGROUND
The American Joint Committee on Cancer staging and other prognostic tools fail to account for stage-independent variability in outcome. We developed a prognostic classifier adding Immunoscore to clinicopathological and molecular features in patients with stage III colon cancer.
METHODS METHODS
Patient (n = 559) data from the FOLFOX arm of adjuvant trial NCCTG N0147 were used to construct Cox models for predicting disease-free survival (DFS). Variables included age, sex, T stage, positive lymph nodes (+LNs), N stage, performance status, histologic grade, sidedness,
RESULTS RESULTS
Poorer DFS was found for tumors that were T4 vs T3 (hazard ratio [HR] = 1.76, 95% confidence interval [CI] = 1.19 to 2.60;
CONCLUSIONS CONCLUSIONS
The Immunoscore can enhance the accuracy of survival prediction among patients with stage III colon cancer.

Identifiants

pubmed: 32455336
doi: 10.1093/jncics/pkaa023
pii: pkaa023
pmc: PMC7236783
doi:

Types de publication

Journal Article

Langues

eng

Pagination

pkaa023

Subventions

Organisme : NCI NIH HHS
ID : U10 CA180868
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180835
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA210509
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA232760
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180882
Pays : United States
Organisme : NCI NIH HHS
ID : U24 CA196171
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180820
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180888
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180821
Pays : United States
Organisme : NCI NIH HHS
ID : U24 CA114740
Pays : United States

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press.

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Auteurs

Frank A Sinicrope (FA)

Division of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.

Qian Shi (Q)

Alliance Statistics and Data Center, Rochester, MN, USA.

Tyler J Zemla (TJ)

Alliance Statistics and Data Center, Rochester, MN, USA.

Bernhard Mlecnik (B)

INSERM, UMRS 1138, Laboratory of Integrative Cancer Immunology, Université Paris Descartes, Paris, France.
Inovarion, Paris, France.

Al B Benson (AB)

Northwestern University, Chicago, IL, USA.

Sharlene Gill (S)

British Columbia Cancer Agency- Vancouver Cancer Centre, Vancouver, BC, Canada.

Richard M Goldberg (RM)

West Virginia Cancer Institute, Morgantown, WV, USA.

Morton S Kahlenberg (MS)

Surgical Oncology Associates of South Texas, San Antonio, TX, USA.

Suresh G Nair (SG)

Lehigh Valley Hospital, Allentown, PA, USA.

Anthony F Shields (AF)

Karmanos Cancer Institute, Detroit, MI, USA.

Thomas C Smyrk (TC)

Division of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.

Jerome Galon (J)

INSERM, UMRS 1138, Laboratory of Integrative Cancer Immunology, Université Paris Descartes, Paris, France.

Steven R Alberts (SR)

Division of Oncology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.

Classifications MeSH