Prognostic markers for patient outcome following vaccination with multiple MHC Class I/II-restricted WT1 peptide-pulsed dendritic cells plus chemotherapy for pancreatic cancer

Anticancer Res. 2015 Jan;35(1):555-62.

Abstract

Background/aim: Treatment combining dendritic cells (DCs) pulsed with three types of major histocompatibility complex (MHC) class I and II (DC/WT1-I/II)-restricted Wilms' tumor 1 (WT1) peptides with chemotherapy may stabilize disease in pancreatic cancer patients.

Materials and methods: Laboratory data from seven patients with pancreatic cancer who underwent combined DC/WT1-I/II vaccination and chemotherapy were analyzed. The DC phenotypes and plasma cytokine profiles were analyzed via flow cytometry.

Results: The post-treatment neutrophil to lymphocyte (N/L) ratio was a treatment-related prognostic factor for better survival. Moreover, the mean fluorescence intensities (MFIs) of human leukocyte antigen (HLA)-DR and cluster of differentiation (CD)83 on DCs were significantly increased after chemoimmunotherapy. Interestingly, interleukin (IL)-6 level in plasma was significantly increased after chemoimmunotherapy in non-super-responders.

Conclusion: An increased N/L ratio, as well as HLA-DR and CD83 MFI levels may be prognostic markers of longer survival in patients with advanced pancreatic cancer who undergo chemoimmunotherapy.

Keywords: Cytokine; MHC class II; WT1; chemoimmunotherapy; dendritic cell; pancreatic cancer; vaccine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / immunology
  • Adenocarcinoma / mortality
  • Adenocarcinoma / secondary
  • Adenocarcinoma / therapy*
  • Adult
  • Aged
  • Antimetabolites, Antineoplastic / therapeutic use
  • Biomarkers, Tumor
  • Cancer Vaccines / administration & dosage
  • Cancer Vaccines / immunology*
  • Cells, Cultured
  • Combined Modality Therapy
  • Cytokines / blood
  • Dendritic Cells / immunology
  • Dendritic Cells / transplantation
  • Deoxycytidine / analogs & derivatives
  • Deoxycytidine / therapeutic use
  • Female
  • Gemcitabine
  • Histocompatibility Antigens Class I / immunology*
  • Histocompatibility Antigens Class II / immunology*
  • Humans
  • Lymphocyte Count
  • Male
  • Middle Aged
  • Neutrophils / immunology
  • Pancreatic Neoplasms / immunology
  • Pancreatic Neoplasms / mortality
  • Pancreatic Neoplasms / pathology
  • Pancreatic Neoplasms / therapy*
  • Peptide Fragments / immunology
  • Prognosis
  • Treatment Outcome
  • Vaccination
  • WT1 Proteins / immunology*

Substances

  • Antimetabolites, Antineoplastic
  • Biomarkers, Tumor
  • Cancer Vaccines
  • Cytokines
  • Histocompatibility Antigens Class I
  • Histocompatibility Antigens Class II
  • Peptide Fragments
  • WT1 Proteins
  • WT1 protein, human
  • Deoxycytidine
  • Gemcitabine