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Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

3029 - Alterations in peripheral T cell subsets, T cell Activation Markers and Immune Checkpoint Molecules in advanced Pancreatic Cancer Patients Receiving FOLFIRINOX or Gemcitabine + Nab-Paclitaxel

Date

20 Oct 2018

Session

Poster display session: Biomarkers, Gynaecological cancers, Haematological malignancies, Immunotherapy of cancer, New diagnostic tools, NSCLC - early stage, locally advanced & metastatic, SCLC, Thoracic malignancies, Translational research

Topics

Tumour Site

Pancreatic Adenocarcinoma

Presenters

Lauren Sams

Citation

Annals of Oncology (2018) 29 (suppl_8): viii400-viii441. 10.1093/annonc/mdy288

Authors

L.E. Sams1, S. Kruger1, V. Heinemann1, D. Bararia2, S. Haebe1, S. Alig1, B. Westphalen1, M. Haas1, T. Kirchner3, S. Ormanns4, S. Endres5, O. Weigert2, M. von Bergwelt-Baildon1, S. Kobold5, F. Rataj5, S. Boeck1

Author affiliations

  • 1 Medizinische Klink Und Poliklinik Iii Großhadern, LMU Klinikum der Universität München, 81377 - Munich/DE
  • 2 Experimentelle Leukämie- Und Lymphom-forschung (ellf), Medizinische Klinik und Poliklinik III Ludwigs Maximilians Universität, 81377 - Munich/DE
  • 3 Pathologisches Institut, Ludwig Maximilians Universität - Campus Innenstadt, 80377 - Munich/DE
  • 4 Pathologisches Institut, Ludwig Maximilians Universität - Campus Innenstadt, 80337 - Munich/DE
  • 5 Abteilung Für Klinische Pharmakologie, Medizinische Klinik Iv, Ludwig Maximilians Universität - Campus Innenstadt, 80336 - Munich/DE

Resources

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Abstract 3029

Background

Efforts to develop successful immunotherapeutic treatments in pancreatic cancer have failed so far. One possible strategy might be the combination of established chemotherapeutic regimens (FOLFIRINOX or gemcitabine plus nab-paclitaxel [gem/nab-pac]) with checkpoint inhibitors. The goal of the present pilot study is to provide a better understanding of alterations in the expression of T cell activation markers and immune checkpoint molecules in patients with advanced pancreatic cancer receiving FOLFIRINOX or gem/nab-pac.

Methods

We conducted a prospective single-center study with selected advanced pancreatic cancer patients who received FOLFIRINOX or gem/nab-pac between 2015 and 2017. Blood samples (15 ml heparinized blood, 10 ml serum) were taken at day 1 and 30 of first-line chemotherapy. Ficoll density gradient separation was used to isolate peripheral blood mononuclear cells (PBMCs). After short-term storage at -80 °C, flow cytometry was performed using a LSR Fortessa flow cytometer (BD Biosciences). CD3+ CD4+ and CD3+ CD8+ T cell count as well as the expression of FoxP3, PD-1, CTLA4, CCR7, CD62L, CD69, Tim3 and LAG 3 on CD3+ T cells was analyzed.

Results

25 eligible patients were included in the study. Two consecutive blood samples were available for 21 of these patients (FOLFIRINOX: n = 18, gem/nab-pac: n = 3). We found a broad variability within T cell subsets and change of expression in T cell activation/immune checkpoint molecules during therapy. While the majority of patients (n = 13/21, 62%) is still in follow-up, first results indicate a correlation of an increase of FOXP3+ T cells in peripheral blood during chemotherapy and worse outcome. No correlation between increase of PD-1 on peripheral T cells and prognosis was observed.

Conclusions

A comprehensive RNA based (nanostring nCounter®) analysis of intratumoral immune cell infiltration of all included patients is currently ongoing. It will provide further insights on the interplay between tumoral and peripheral (T cell) immunity during chemotherapy in advanced pancreatic cancer.

Clinical trial identification

Legal entity responsible for the study

Stefan Böck.

Funding

Friedrich-Baur-Stiftung.

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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