Wijaya Wynne, Khattak Muhammad Adnan, Abed Afaf, Meniawy Tarek, Millward Michael, Gray Elin, Oey Oliver
Department of Oncology, University of Oxford, Oxford, United Kingdom.
Department of Medical Oncology, Fiona Stanley Hospital, Murdoch, Perth, Australia.
Cancer Invest. 2025 Nov;43(10):945-957. doi: 10.1080/07357907.2025.2586257. Epub 2025 Nov 13.
Metastatic melanoma carries a poor prognosis. Immune checkpoint inhibitors (ICIs) have improved outcomes, but responses remain variable, highlighting the need for simple prognostic biomarkers. Inflammatory markers such as neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and lactate dehydrogenase (LDH) reflect tumour burden and inflammation, though their clinical utility is unstandardised.
We retrospectively analysed 103 metastatic melanoma patients treated with anti-PD-1 monotherapy at two centres in Western Australia (2014-2020). Baseline NLR, PLR, and LDH were assessed within 30 days pre-treatment. Outcomes included clinical benefit, progression-free survival (PFS), and overall survival (OS).
Poor ECOG performance status (PS ≥2) (RR 2.39, 95% CI 1.48-3.86) and elevated LDH (≥250 U/L) (RR 1.68, 95% CI 1.21-2.31) were associated with no clinical benefit ( < 0.001). NLR ≥5 predicted significantly worse OS (9.1 vs 28.2 months; HR 8.54, 95% CI 2.58-28.32; < 0.001). Elevated LDH predicted shorter OS (6.0 vs 50.3 months; HR 3.68, 95% CI 1.65-8.21; = 0.002) and PFS (19.0 months vs not reached; HR 2.51, 95% CI 1.37-4.72; = 0.004).
ECOG PS ≥2 and elevated NLR were associated with no clinical benefit, while elevated NLR and LDH independently predicted poorer survival. These markers may serve as practical prognostic tools in metastatic melanoma treated with ICIs.