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Poster session 07

29P - Dynamic NK cell activity as a prognostic biomarker in non-small cell lung cancer treated with curative surgery

Date

10 Sep 2022

Session

Poster session 07

Topics

Clinical Research;  Tumour Immunology;  Translational Research;  Molecular Oncology

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Sara Wen

Citation

Annals of Oncology (2022) 33 (suppl_7): S4-S18. 10.1016/annonc/annonc1035

Authors

S.W.C. Wen1, L. Nederby2, T.F. Hansen3, A. Jakobsen3, O. Hilberg4

Author affiliations

  • 1 Department Of Oncology, Vejle Hospital, part of University Hospital of Southern Denmark, 7100 - Vejle/DK
  • 2 Department Of Biochemistry, Vejle Hospital, part of University Hospital of Southern Denmark, 7100 - Vejle/DK
  • 3 Department Of Oncology, Vejle Hospital, part of University Hospital of Southern Denmark, 5500 - Middelfart/DK
  • 4 Department Of Medicine, Vejle Hospital, part of University Hospital of Southern Denmark, 7100 - Vejle/DK

Resources

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Abstract 29P

Background

Surgery holds curative potential in non-small cell lung cancer (NSCLC), but around 50% of the patients will still experience disease recurrence. Natural Killer (NK) cells are important as a part of the host immune defense against cancer, and NK cell activity (NKA) has been suggested as a prognostic biomarker.

Methods

Patients with NSCLC eligible for surgery with curative intent were prospectively enrolled. Blood was sampled at baseline, 2-7 weeks post-operatively, and at the first follow-up. Interferon gamma (IFNg) as a surrogate for NKA was measured using the NK Vue® assays (NKMAX, Seongnam-si, South Korea). A cutoff of >250 pg/mL was used to define a normal test according to the manufacturer’s instructions.

Results

We enrolled 78 patients, who received curatively intended surgery for NSCLC. The median NKA was 569 pg/mL, 357 pg/mL, and 784 pg/mL, respectively, at baseline, 2-7 weeks post-surgery, and follow-up (1-10 months). There was no significant difference in NKA between the time-points. A division of the patients into two groups according to NKA cut-off at baseline resulted in a difference in overall survival (OS) (p=0.014) but not in recurrence free survival (RFS) (p=0.548). A further division according to NKA dynamics resulted in three groups: The NKA-low group had NKA <250 pg/mL at all available time-points (n=19). The NKA-mixed group had NKA of varying levels (n=21). The NKA-high group had NKA >250 pg/mL at all available time-points (n=38). This grouping had a statistically significant prognostic impact on OS (p=0.027), but not on RFS (p=0.728). The hazard ratio was 5.36 (95% CI 1.39-20.64) for the NKA-low group compared to the NKA-high group. Table: 29P

Patient characteristics

Patient characteristics Total n=78 n (%) or median (range)
Sex, male 37 (47%)
Age, years 69 (44-85)
Histology, adenocarcinoma 47 (60%)
Histology, squamous cell carcinoma 25 (32%)
Histology, other 6 (8%)
Stage I 39 (50%)
Stage II 23 (29%)
Stage III 16 (21%)
Post-operative complications 21 (27%)
Adjuvant chemotherapy 23 (29%)

Conclusions

The dynamics of NK cell activity may be used for a prognostic subclassification of NSCLC patients undergoing surgery with curative intent.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Thora og Viggo Groves Mindelegat, AP Møller Fonden, Kleins Mindelegat, and grants within the Department of Oncology, Vejle Hospital.

Disclosure

S.W.C. Wen, L. Nederby, T.F. Hansen, A. Jakobsen, O. Hilberg: Other, Institutional, Product Samples: NK Max.

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