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Poster Display session 1

3583 - Immune microenvironment modulation by p14/ARF in Malignant Pleural Mesothelioma


28 Sep 2019


Poster Display session 1


Tumour Site



Giulia Pasello


Annals of Oncology (2019) 30 (suppl_5): v747-v755. 10.1093/annonc/mdz266


G. Pasello1, L. Urso2, A. Boscolo2, F. Pezzuto3, M. Silic-Benussi4, S. Vuljian5, S. Frega1, L. Bonanno1, M. Schiavon3, F. Rea6, V. Ciminale4, P.F. Conte7, F. Calabrese3

Author affiliations

  • 1 Oncology 2, Istituto Oncologico Veneto IRCCS, 35128 - Padova/IT
  • 2 Department Of Surgery, Oncology And Gastroenterology, University of Padova, 35128 - Padova/IT
  • 3 Pathology Unit, Department Of Cardiac,thoracic, Vascular Sciences And Public Health, University of Padova, 35128 - Padova/IT
  • 4 Immunology And Molecular Oncology Unit, Istituto Oncologico Veneto IRCCS, 35128 - Padova/IT
  • 5 Pathology Unit, Department Of Cardio-thoracic And Vascular Sciences, University of Padova, 35128 - Padova/IT
  • 6 Thoracic Surgery Unit, Department Of Cardiac,thoracic, Vascular Sciences And Public Health, University of Padova, 35128 - Padova/IT
  • 7 Surgery Oncology And Gastroenterology, Università degli Studi di Padova, 35128 - Padova/IT


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Abstract 3583


Tumor Associated Macrophages (TAMs) and ARF-MDM2 pathway seem to be interconnected actors in malignant pleural mesothelioma (MPM) pathogenesis, treatment outcome and prognosis. On the basis of such evidence, this prospective study aims at comparing tumor immune microenvironment (TME) and checkpoint expression (PD-L1) in naïve tumor samples and immune cells in blood samples of ARF+ vs. ARF- MPM.


Tumor samples were collected at the baseline (T0) in all enrolled patients and at the time of surgery (T1) in resectable patients. Immunohistochemistry was carried out to evaluate p14/ARF, PD-L1, CD3+, CD4+, CD8+ T lymphocytes; CD20+ B-lymphocytes; CD68+ macrophages. Blood samples were collected in a subset of patients at T0 and T1 and analyzed for CD3+CD4+, CD3+CD8+, CD4+CD25+FoxP3+ peripheral T lymphocytes, CD68 + (total) and CD163 + (M2-like) peripheral monocytes by flow cytometry analysis.


Preliminary data on the first 52 chemonaive MPM samples (32 epithelioid, 16 biphasic and 4 sarcomatoid) were evaluated. P14/ARF was detected in 11 patients (21%). P14/ARF+ cases were characterized by higher CD4+ T-lymphocyte percentage (median value 10% vs 1%, p = 0.05), mainly in peritumoral areas, while p14/ARF – cases were characterized by higher CD163+ M2 macrophages percentage (50% vs 40% in p14/ARF+ cases) and higher CD163+/CD68+ ratio (1.3 vs. 1 in p14/ARF+ cases), even though without statistical significance. Paired (T0 and T1) blood samples of five patients were also assessed for CD8+ and CD4+CD25+FoxP3+ T-reg lymphocytes levels change before and after chemotherapy. We observed a T-reg decrease in 2 patients achieving a disease control to first-line platinum-based chemotherapy, while an increase in 3 progressing patients, without major difference between p14/ARF + and p14/ARF- cases.


p14ARF+ MPM samples seem to be characterized by lower CD163+ M2-polarized macrophages and higher CD4+ T lymphocytes. The amount of T-reg in blood samples may be useful to anticipate radiological and/or clinical progression to chemotherapy. Larger case series and wider TME characterization in tissue and immune cells quantification in blood samples are needed to validate our preliminary findings and will be presented at the conference.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Istituto Oncologico Veneto IRCCS.


Has not received any funding.


All authors have declared no conflicts of interest.

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