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
1171P - Evaluation of the transcriptomic presence of tumor associated antigens (TAAs) from antibody drug conjugates (ADCs) and PD-L1 in melanoma: Options for new clinical opportunities
Presenter: Jorge Bartolome
Session: Poster session 13
1172P - Analysis of the microbiome of metastatic melanoma patients with complete response to immunotherapy
Presenter: Marin Golcic
Session: Poster session 13
1173P - NRAS mutation as an independent prognostic factor for resectable Chinese acral melanoma
Presenter: Yu Xu
Session: Poster session 13
1174P - Sex differences in advanced melanoma in Spain: Results from the prospective real-world study GEM 1801
Presenter: Eva Muñoz Couselo
Session: Poster session 13
1175P - Return to work after neoadjuvant versus adjuvant immunotherapy in stage III melanoma patients
Presenter: Judith Lijnsvelt
Session: Poster session 13
1176P - Planned drug holidays during immunotherapy in advanced and metastatic melanoma patients: A nation-wide study
Presenter: Anna Czarnecka
Session: Poster session 13
1177P - Assessment of tumour burden reduction per photography vs magnetic resonance imaging in patients with locally advanced basal cell carcinoma receiving sonidegib 200 mg
Presenter: Ralf Gutzmer
Session: Poster session 13
1178P - Melanoma incidence rises for pediatrics: 15-year nationwide retrospective cohort study in Korea (2004-2019)
Presenter: Jisu Oh
Session: Poster session 13
1179P - The underestimated skin cancer risk after liver transplantation: A meta-analysis of 147154 patients
Presenter: Amr Ehab El-Qushayri
Session: Poster session 13