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PMID: 24691640 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Prognostic and predictive values of the immunoscore in patients with rectal cancer.

Anitei MG, Zeitoun G, Mlecnik B, Marliot F, Haicheur N, Todosi AM, Kirilovsky A, Lagorce C, Bindea G, Ferariu D, Danciu M, Bruneval P, Scripcariu V, Chevallier JM, Zinzindohoué F, Berger A, Galon J, Pagès F

Abstract

To determine whether the tumor immune infiltrate, as recently evaluated with the Immunoscore methodology, could be a useful prognostic marker in patients with rectal cancers. The influence of the immune infiltrate on patient's outcome was investigated in patients with or without preoperative chemoradiation therapy (pCRT). The density of total (CD3(+)) and cytotoxic (CD8(+)) T lymphocytes was evaluated by immunohistochemistry and quantified by a dedicated image analysis software in surgical specimens of patients with rectal cancer (n = 111) who did not receive pCRT and in tumor biopsies performed before pCRT from additional 55 patients. The results were correlated with tumor recurrence, patient's survival, and response to pCRT. The densities of CD3(+) and CD8(+) lymphocytes and the associated Immunoscore (from I0 to I4) were significantly correlated with differences in disease-free and overall survival (HR, 1.81 and 1.72, respectively; all P < 0.005). Cox multivariate analysis supports the advantage of the Immunoscore compared with the tumor-node-metastasis (TNM) staging in predicting recurrence and survival (all P < 0.001). Lymph node ratio added information in a prognostic model (all P < 0.05). In addition, high infiltration of CD3(+) and CD8(+) lymphocytes in tumor biopsies was associated with downstaging of the tumor after pCRT (CD3(+) cells; Fisher exact test P = 0.01). The Immunoscore could be a useful prognostic marker in patients with rectal cancer treated by primary surgery. The determination of the immune infiltrate in biopsies before treatment could be a valuable information for the prediction of response to pCRT.

MeSH Terms
Aged Aged, 80 and over Biopsy CD3 Complex/immunology CD8-Positive T-Lymphocytes/immunology Combined Modality Therapy Female Humans Lymphatic Metastasis/immunology,pathology Male Middle Aged Neoplasm Recurrence, Local/drug therapy,immunology,pathology,radiotherapy Neoplasm Staging Prognosis Radiotherapy Dosage Rectal Neoplasms/drug therapy,immunology,pathology,radiotherapy Treatment Outcome
Chemicals
CD3 Complex
Authors & Affiliations
18 authors, click to expand affiliations / ORCID
Anitei Maria-Gabriela
Authors' Affiliations: Department of Surgery, University of Medicine and Pharmacy "Gr T Popa"; Departments of Pathology and Surgical Oncology, Regional Institute of Oncology; Department of Pathology St. Spiridon Hospital, Iasi, Romania; Department of General and Digestive Surgery of the Georges Pompidou European Hospital and Department of Pathology of the Georges Pompidou European Hospital, Laboratory of Immunology, Immunomonitoring platform of the Georges Pompidou European Hospital, AP-HP; Laboratory of Integrative Cancer Immunology, Institut national de la santé et de la recherche medicale (INSERM) U872, Cordeliers Research Center; Paris-Descartes University; Pierre et Marie Curie-Paris 6 University, Paris; and Department of Pathology, Avicenne Hospital, Bobigny, France.
Zeitoun Guy
Mlecnik Bernhard
Marliot Florence
Haicheur Nacilla
Todosi Ana-Maria
Kirilovsky Amos
Lagorce Christine
Bindea Gabriela
Ferariu Dan
Danciu Mihai
Bruneval Patrick
Scripcariu Viorel
Chevallier Jean-Marc
Zinzindohoué Franck
Berger Anne
Galon Jérôme
Pagès Franck
Article Info
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
Abbr.
Clin Cancer Res
ISSN
1557-3265
Published
2014-04-01
Pages
1891-9
Language
English
Region
United States
NLM ID
9502500
Subset
IM
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