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Poster Display session

764P - Neutrophil to lymphocyte ratio (NLR) as a prognostic biomarker in melanoma patients treated with immune checkpoint inhibitors

Date

07 Dec 2024

Session

Poster Display session

Presenters

Oliver Oey

Citation

Annals of Oncology (2024) 35 (suppl_4): S1679-S1697. 10.1016/annonc/annonc1699

Authors

O. Oey1, W. Wijaya2, M.A. Khattak3, A. Abed4, T. Meniawy5, A. Reid6, L. Calapre6, M. Millward7, E.S. Gray8

Author affiliations

  • 1 Medicine Department, University of Western Australia, 6009 - Perth/AU
  • 2 Oncology, University of Oxford, OX3 7DQ - Oxford/GB
  • 3 Department Of Medical Oncology, Fiona Stanley Hospital, WA 6009 - Nedlands , Australien/AU
  • 4 Oncology Department, Peel Health Campus, 6210 - Mandurah/AU
  • 5 Oncology, Sir Charles Gairdner Hospital, 6009 - Nedlands/AU
  • 6 Centre For Precision Health, School Of Medical And Health Sciences, Edith Cowan University, 6027 - Perth/AU
  • 7 School Of Medicine, University of Western Australia, 6009 - Perth/AU
  • 8 School Of Medical And Health Sciences, Edith Cowan University, 6027 - Perth/AU

Resources

This content is available to ESMO members and event participants.

Abstract 764P

Background

Systemic inflammation has been shown to promote tumorigenesis, tumour progression and confers poorer survival. An elevated neutrophil to lymphocyte ratio (NLR), a marker of systemic inflammation, has been linked to inferior patient outcomes in various solid malignancies. Real-world data on the relationship between NLR with survival outcomes in melanoma patients who are receiving immune-checkpoint inhibitors (ICI) remains scarce. We aim to investigate the role of NLR as a prognostic biomarker in metastatic melanoma patients treated with ICI (either pembrolizumab or nivolumab).

Methods

We retrospectively reviewed the records of 118 metastatic melanoma patients treated with either pembrolizumab or nivolumab between August 2014 to January 2020 at our institution. NLR values were grouped into two categories: ≤5 and >5. Median overall survival (OS) and progression free survival (PFS) were obtained. Univariate analyses were performed using Cox regression model. Multivariate analyses were performed while controlling for age, gender, prior therapy, BRAF mutation status, ECOG performance status and presence of liver and brain metastases.

Results

The mean age was 68±12. Majority (66.9%) were female, had only one line of treatment (72.9%) and were BRAF wild type (66.9%). Most did not have brain metastases (80.5%) and liver metastases (86.4%). Most were ECOG 0 or 1 (69.5%). The median OS for patients in the NLR>5 and NLR≤5 group was 12.2 months and undefined (more than 50% of patients were still alive at end of study) respectively. The median PFS for patients in the NLR>5 and NLR≤5 group was 6.0 months and 28.1 months respectively. On univariate analysis, patients with baseline NLR >5 had significantly worse OS (HR 3.07; 95% CI 1.61-5.82; P=0.001) and PFS (HR 1.91; 95% CI 1.06-3.45; P=0.031) than patients with NLR≤5. On multivariate analyses, the prognostic value of NLR significantly improved for both OS (HR 5.69; 95% CI 2.31-14.04; P≤0.0001) and PFS (HR 2.77; 95% CI 1.32-5.80; P=0.007).

Conclusions

Our study suggests that pretreatment NLR>5 is associated with worse survival outcomes. NLR is a cheap and readily-available biomarker which could be used to prognosticate metastatic melanoma patients who are receiving ICI.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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