Prognostic and predictive value of immunological parameters for chemoradioimmunotherapy in patients with pancreatic adenocarcinoma
Background: Chemoradioimmunotherapy of patients with pancreatic adenocarcinoma from the CapRI trial did not show any benefit of interferon- α in addition to a 5-fluorouracil (5FU)-based treatment. The aim of this study was to identify immunological parameters in patients from this trial to be used f...
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Veröffentlicht in: | British journal of cancer 2015-03, Vol.112 (6), p.1027-1036 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background:
Chemoradioimmunotherapy of patients with pancreatic adenocarcinoma from the CapRI trial did not show any benefit of interferon-
α
in addition to a 5-fluorouracil (5FU)-based treatment. The aim of this study was to identify immunological parameters in patients from this trial to be used for predictive and/or prognostic purposes.
Methods:
The following methods were used: tumour immunohistology, FACS analyses, cytokine measurement, as well as cytotoxicity and ELIspot. Immunological parameters were correlated with patients’ survival using the Kaplan–Meier method.
Results:
Irrespective of therapy type, high lymphocyte accumulation in tumours and frequencies of NK cells and effector (eff) CD8
+
T cells in peripheral blood of the patients were associated with patients’ survival. Amount of CD3
+
and effector-memory CD8
+
blood lymphocytes, expression of CD152 and interleukin (IL)-2 serum level showed a predictive value for chemoradioimmunotherapy. Tumoural accumulation of CD3
+
and CD8
+
cells was predictive for outcome of chemotherapy alone. Besides, we identified the frequencies of CD3
+
lymphocytes, effCD8
+
T cells and NK cells in the peripheral blood of the patients, and IL-10 amount in serum, to be predictive values for 5FU-based chemotherapy.
Conclusions:
Immunological parameters, identified in this trial as possible markers, may be of interest in personalized medicine towards the improvement of the treatment and prognosis of pancreatic carcinoma patients. |
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ISSN: | 0007-0920 1532-1827 |
DOI: | 10.1038/bjc.2015.72 |