Abstract 1122P
Background
Immune checkpoint inhibitors (ICI) targeting cytotoxic T-lymphocyte-associated protein 4 and programmed cell death protein 1 are now the standard of care for patients with advanced melanoma, with an improvement in overall survival (OS) and quality of life. Elevated neutrophil to lymphocyte ratio (NLR) and systemic inflammatory index (SII) have been reported associated with poor survival in cancer patients, including those with ICI. The aim of this study was to determine the clinical significance of pre-treatment NLR and SII as prognostic indicator in metastatic melanoma patients treated with ICI.
Methods
Retrospective, multicentric study of metastatic melanoma patients who received ICI between 2016-2022 in two hospitals in Portugal. The SII [platelets x neutrophil/lymphocyte ratio] and NLR were calculated before the beginning of ICI. SII was considered high if > 572 and NLR was considered high if >5. Data was collected from clinical records. Statistical analysis was performed with SPSSv26. Progression free survival (PFS) and OS were assessed using Kaplan-Meier plots and log-rank testing.
Results
Eighty-nine patients were enrolled, 57 were male, mean age 68 years old. Seventy-six patients had cutaneous, 10 mucosal and 3 uveal melanoma. The type of ICI was nivolumab in 36 patients, ipilimumab/nivolumab in 34 and pembrolizumab in 19. With a median follow-up of 19 months, the median PFS and OS was 11 and 15 months, respectively. NLR was high in 12 patients. The median PFS was 3 months in NLR high vs 25 months in NLR low patients and OS was 13 months in NLR high vs 32 months. However, these differences were not statistically significant. A total of 53 patients were presented with SII high. In this group, the median PFS was 10 months vs 22 months in SII low patients (p=0.017) and the median OS was 17 months vs 32 months (p=0.032).
Conclusions
The present study suggests that elevated SII may be associated with a worse PFS and OS in metastatic melanoma patients, however, this association was not demonstrated for NLR. Thus, SII could be a prognostic value on advanced/metastatic melanoma in patients under ICI and could be an important tool in the management of these patients.
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.
Resources from the same session
1130P - Tebentafusp (tebe) in an ongoing cohort of 72 French patients (pts) with metastatic uveal melanoma (mUM)
Presenter: Leah Mailly-Giacchetti
Session: Poster session 13
1131P - Management of metastatic uveal melanoma (MUM) patients on tebentafusp in a real-world setting
Presenter: Mauricio Fernando Ribeiro
Session: Poster session 13
1132P - Chemokine expression in uveal melanoma and association with tumor genetics and response to immunotherapy
Presenter: Aparna Nallagangula
Session: Poster session 13
1133P - SF3B1 mutation predicts improved overall survival in metastatic uveal melanoma patients: Molecular and clinical correlates
Presenter: Luis del Carpio Huerta
Session: Poster session 13
1134P - Safety and efficacy of low dose (LD) ipilimumab (Ipi) + pembrolizumab (pem) in checkpoint inhibitor (CPI) naïve patients (pts) with melanoma brain metastases (MBM)
Presenter: Isabella Glitza
Session: Poster session 13
1135P - Comparison of intracranial (IC) response assessment criteria in patients (pts) with melanoma brain metastases (MBM) treated with combination nivolumab (NIVO) plus ipilimumab (IPI) in CheckMate 204
Presenter: Raymond Huang
Session: Poster session 13
1136P - Regorafenib combined with BRAF-/MEK-inhibitors for the treatment of refractory melanoma brain metastases
Presenter: Iris Dirven
Session: Poster session 13
1138P - Intralesional administration of L19IL2/L19TNF in difficult-to-treat non-melanoma skin cancer shows a favorable safety profile and preliminary clinical activity
Presenter: Lukas Flatz
Session: Poster session 13
1139P - Final results of a phase II study of pembrolizumab as first-line treatment in advanced cutaneous squamous cell carcinomas (CSCCs)
Presenter: Eve Maubec
Session: Poster session 13