Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster Display session

92P - Exploring immune dysfunction in surgically treated early stage NSCLC

Date

03 Apr 2022

Session

Poster Display session

Topics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Laura Sellmer

Citation

Annals of Oncology (2022) 33 (suppl_2): S71-S78. 10.1016/annonc/annonc857

Authors

L. Sellmer1, J. Kovács2, J. Walter3, J. Kumbrink4, J. Neumann1, D. Kauffmann-Guerrero3, R. Kiefl1, C. Schneider2, A. Jung1, J. Behr1, A. Tufman5

Author affiliations

  • 1 University Hospital LMU Munich, Munich/DE
  • 2 University Hospital, LMU Munich, Munich/DE
  • 3 LMU Klinikum der Universität München, Munich/DE
  • 4 University Hospital LMU Munich, 80337 - Munich/DE
  • 5 LMU Klinikum der Universität München, 80336 - Munich/DE

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 92P

Background

Tumor tissue as well as regional lymph nodes are removed during curative surgery for early-stage non-small cell lung cancer (NSCLC). These tissues provide a snapshot of the patient's immune system at the time of surgery. We performed immune cell transcriptomics in matched tumor tissue, tumor bearing (tb) and non-tumor bearing (ntb) N1 as well as N2 lymph nodes (LNs) in patients with NSCLC and investigated their relation to survival.

Methods

Hospital databases were screened for surgically treated NSCLC patients for whom tumor tissue, tbLNs as well as N1 and N2 ntbLNs were available. Clinical as well as demographic data were extracted from hospital records. Expression profiling of 770 immune-related genes was performed using the PanCancer IO 360 panel by NanoString Technologies. We analyzed association between transciptomics data and overall survival (OS) and progression-free survival (PFS) using stepwise Cox regression.

Results

We identified 190 surgically treated patients in hospital databases. 16 of these patients fulfilled inclusion criteria and had sufficient archived tissue available. The Tumor Immune Dysfunction and Exclusion (TIDE) score in N1 and N2 tumor-free lymph nodes was associated with OS (p=0.009, HR=0.64) as well as PFS (p=0.026, HR=0.68). Of the 16 patients in this study, only four patients (25%) showed consistently positive or negative TIDE scores across all four examined tissues. Five patients (31%) showed discrepancies in only one tissue and the remaining seven (44%) patients showed two negative and two positive scores. Cytotoxic T-cells were the only cell type to differ between TIDE Low and TIDE High patients in more than one tissue.

Conclusions

TIDE scores in tumor and regional lymph nodes may indicate a dysfunctional immune status and can predict postoperative survival in NSCLC.

Legal entity responsible for the study

Medizinische Klinik V, University Hospital Munich.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.