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Expression of Programmed Cell Death Protein 1 by Tumor-Infiltrating Lymphocytes and Tumor Cells is Associated with Advanced Tumor Stage in Patients with Esophageal Adenocarcinoma.
Kollmann, Dagmar; Ignatova, Desislava; Jedamzik, Julia; Chang, Yun-Tsan; Jomrich, Gerd; Paireder, Matthias; Kristo, Ivan; Kazakov, Dmitry; Michal, Michal; Cozzio, Antonio; Hoetzenecker, Wolfram; Schatton, Tobias; Asari, Reza; Preusser, Matthias; Guenova, Emmanuella; Schoppmann, Sebastian F.
Afiliación
  • Kollmann D; Department of Surgery, Comprehensive Cancer Center Vienna, Upper-GI-Service, GET-Unit, Medical University of Vienna, Vienna, Austria.
  • Ignatova D; Department of Dermatology, University Hospital Zürich, University of Zurich, Zurich, Switzerland.
  • Jedamzik J; Department of Surgery, Comprehensive Cancer Center Vienna, Upper-GI-Service, GET-Unit, Medical University of Vienna, Vienna, Austria.
  • Chang YT; Department of Dermatology, University Hospital Zürich, University of Zurich, Zurich, Switzerland.
  • Jomrich G; Department of Surgery, Comprehensive Cancer Center Vienna, Upper-GI-Service, GET-Unit, Medical University of Vienna, Vienna, Austria.
  • Paireder M; Department of Surgery, Comprehensive Cancer Center Vienna, Upper-GI-Service, GET-Unit, Medical University of Vienna, Vienna, Austria.
  • Kristo I; Department of Surgery, Comprehensive Cancer Center Vienna, Upper-GI-Service, GET-Unit, Medical University of Vienna, Vienna, Austria.
  • Kazakov D; Department of Pathology, Faculty of Medicine in Plzen and Charles University Hospital Plzen, Biomedical Center, Charles University, Pilsen, Czech Republic.
  • Michal M; Department of Pathology, Faculty of Medicine in Plzen and Charles University Hospital Plzen, Biomedical Center, Charles University, Pilsen, Czech Republic.
  • Cozzio A; Department of Dermatology, Kantonspital St. Gallen, University of Zurich, Zurich, Switzerland.
  • Hoetzenecker W; Department of Dermatology, University Hospital Zürich, University of Zurich, Zurich, Switzerland.
  • Schatton T; Department of Dermatology, Kantonspital St. Gallen, University of Zurich, Zurich, Switzerland.
  • Asari R; Department of Dermatology, Kepler University Hospital, Linz, Austria.
  • Preusser M; Department of Dermatology, Harvard Skin Disease Research Center, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Guenova E; Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Schoppmann SF; Department of Surgery, Comprehensive Cancer Center Vienna, Upper-GI-Service, GET-Unit, Medical University of Vienna, Vienna, Austria.
Ann Surg Oncol ; 24(9): 2698-2706, 2017 Sep.
Article en En | MEDLINE | ID: mdl-28429196
ABSTRACT

BACKGROUND:

Despite recent advances in the therapy for adenocarcinoma of the esophagogastric junction (AEG), overall prognosis remains poor. Programmed cell death protein 1 (PD1) is a co-inhibitory receptor primarily expressed by T-cells. Tumor cells can escape anticancer immune responses by triggering the PD1 pathway. Moreover, PD1 receptor engagement on cancer cells may trigger tumor-intrinsic growth signals. This study aimed to evaluate the potential clinical relevance of PD1 expression by tumor-infiltrating lymphocytes (TILs) and cancer cells in the AEG.

METHODS:

Patients with AEG who underwent esophagectomy from 1992 to 2011 were included in the study. Expression of PD1was evaluated by immunohistochemistry and correlated with long-term overall survival (OS), disease-free survival (DFS), and various clinicopathologic parameters.

RESULTS:

Tumor biospecimens from 168 patients were analyzed. In the analysis, 81% of the patients showed high tumoral frequencies (>5%) of PD1-expressing TILs (TIL-PD1+), and 77% of patient tumors harbored high levels (>5%) of PD1+ cancer cells (cancer-PD1+). Expression of PD1 by TILs and cancer cells correlated significantly (p < 0.05) with patients' tumor stage and lymph node involvement. Compared with the patients who had low tumoral frequencies of PD1+ TILs or cancer cells, the TIL-PD1+ and cancer-PD1+ patients demonstrated significantly reduced DFS in the univariate analysis (5-year DFS 73.3 vs. 41.9%, log-rank 0.008 and 71.3 vs. 41.6%, p = 0.008, respectively). Additionally, the cancer-PD1+ patients showed significantly decreased OS in the univariate analysis compared with the cancer-PD1- patients (5-year OS 68.8 vs. 43.5%; p = 0.047). However, these correlations did not reach significance in the multivariate analysis.

CONCLUSIONS:

The PD1 receptor is expressed by both TILs and cancer cells in AEG. High expression of PD1 is associated with advanced tumor stage and lymph node involvement, but not with survival.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Esofágicas / Adenocarcinoma / Linfocitos Infiltrantes de Tumor / Unión Esofagogástrica / Receptor de Muerte Celular Programada 1 Tipo de estudio: Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Surg Oncol Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Esofágicas / Adenocarcinoma / Linfocitos Infiltrantes de Tumor / Unión Esofagogástrica / Receptor de Muerte Celular Programada 1 Tipo de estudio: Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Surg Oncol Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article País de afiliación: Austria