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Long-term immune-modulatory side effects of radiofrequency ablation in patients with liver metastases and hepatocellular carcinoma
Author(s) -
Pietro Di Fazio,
ThaddeusTill Wissniowski,
Thomas M. Gress
Publication year - 2015
Publication title -
hepatoma research
Language(s) - English
Resource type - Journals
eISSN - 2454-2520
pISSN - 2394-5079
DOI - 10.4103/2394-5079.158024
Subject(s) - medicine , hepatocellular carcinoma , radiofrequency ablation , pathogenesis , immune system , cancer research , gastroenterology , ablation , oncology , pathology , immunology
92 Address for correspondence: Dr. Pietro Di Fazio, Department of Visceral, Thoracic and Vascular Surgery, Philipps University of Marburg, Baldingerstrasse, 35041 Marburg, Germany. E-mail: difazio@med.uni-marburg.de Received: 12-02-2015, Accepted: 20-05-2015 ABSTRACT Aim: Used as a palliative therapy for unresectable liver cancer, radiofrequency ablation (RFA) is associated with the induction of immunological responses. Here, we show strong evidence of tumor-specifi c peripheral blood mononuclear cells (PBMCs) 12 months after RFA. Methods: Three patients with colorectal cancer (CRC) metastases to the liver and two patients with primary hepatocellular carcinoma (HCC) were enrolled in this study. PBMC, isolated 12 months after RFA, were stimulated with normal and tumor tissue lysate. Interferon gamma secretion was evaluated by fl ow cytometry and indirectly, by luciferase assay for adenylate kinase activity in PBMC-stimulated lysates of target cells. Baseline data were detected before RFA and 4 weeks after treatment. Results: Two CRC patients and one HCC patient had recurrence-free survival. One patient with CRC developed secondary metastases; one patient with HCC developed a local recurrence. Recurrence-free patients showed a signifi cantly higher cytolytic activity of PBMC against matched tumor cells 12 months after RFA treatment. Interestingly, patients with malignant recurrence showed a decreased cytolytic activity. Conclusion: RFA seems to overcome immune-tolerance toward tumor antigens and/or presents new tumor antigens. Patients seem to benefi t from a prolonged increase in cytolytic activity. The immune-modulatory effects of RFA need further investigations in multimodality anticancer therapies.

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