Abstract 38P
Background
Immune Checkpoint Inhibitors (ICIs) have substantially improved the prognosis of metastatic melanoma. However, not all patients benefit equally. To optimize patient selection for ICIs and minimize immune-related toxicity in those with a low likelihood of response, it is essential to identify predictive biomarkers. Our study assessed the association between certain patient characteristics and response to ICIs, progression-free survival (PFS), and overall survival (OS).
Methods
In this retrospective, observational study, we included 49 patients with metastatic melanoma treated with Pembrolizumab or with Nivolumab + Ipilimumab. Collected parameters included sex, age, BRAF V600E mutation status, localization of metastases, baseline lactate dehydrogenase (LDH) and neutrophil to lymphocyte ratio (NLR), best overall response (bOR) achieved, development and type of immune related adverse events (irAEs), dates of progression and death. All statistical analyses were performed using Jamovi, version 2.5.4.
Results
Most patients (57.1%) received Nivolumab + Ipilimumab, with an Overall Response Rate (ORR) of 35.7%, while ORR for Pembrolizumab was 28.5%. For the entire cohort, median PFS and OS were 9.1 months and 21 months, respectively. We found a significant association between the response to ICIs and irAEs, with a relative risk (RR) of 2.93 (p= 0.01). Cutaneous irAEs, including vitiligo, occurred in 52.4% of patients and were associated with a higher RR of 3.45 (p = 0.003). There was no association between response to ICIs and LDH, NLR, sex, age or BRAF status. Patients with elevated LDH (>245 U/L) had significantly shorter OS than those with normal LDH, with HR: 3.26 (95% CI: 1.16-9.17), p < 0.05. Similarly, patients with elevated NLR (cut-off values: 3.46 for PFS, 4.13 for OS) had significantly shorter PFS and OS than those with low NLR (p < 0.05), with corresponding hazard ratios of 1.23 (95% CI: 1.03-1.47) for PFS and 1.34 (95% CI: 1.09-1.64) for OS.
Conclusions
The development of irAEs, particularly cutaneous irAEs, may serve as an indicator of response to ICIs in metastatic melanoma patients. Baseline LDH and NLR levels have prognostic significance, but are not predictive of response to ICIs.
Editorial acknowledgement
During the preparation of this work the author(s) used ChatGPT in order to rephrase sentences, make them shorter/ more concise in order to better express the meaning and fit inside the character limit. After using this tool/service, the author(s) reviewed and edited the content as needed and take(s) full responsibility for the content of the publication.
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
195P - Anti-CTLA4 therapy leads to early expansion of peripheral Th17 population and induction of Th1 cytokines
Presenter: Mari Nakazawa
Session: Poster Display session
Resources:
Abstract
196P - Single-cell analysis of stage-I high-grade serous ovarian carcinoma reveals the essential role of regulatory T cells in early tumor establishment
Presenter: Joanna Mikulak
Session: Poster Display session
Resources:
Abstract
197P - Comprehensive immunoprofiling of the intratumoral and peripheral T cell receptor gene repertoire in triple-negative breast cancer patients
Presenter: Antonios Mingos
Session: Poster Display session
Resources:
Abstract
198P - Association of types of treatment modalities with expression of T Lymphocytes (CD4, CD8, Treg) in breast cancer patients and their clinical outcome
Presenter: Arshi Rizwan
Session: Poster Display session
Resources:
Abstract
199P - Cancer neutrophil encyclopedia: A deep dive into antigen-presenting warriors
Presenter: Yingcheng Wu
Session: Poster Display session
Resources:
Abstract
200P - CXCR1+ neutrophil infiltration orchestrates response to third-generation EGFR-TKI in EGFR mutant NSCLC
Presenter: Haowei Wang
Session: Poster Display session
Resources:
Abstract
201P - Underlying mechanisms of neutrophil-mediated immunosuppression and resistance to treatment in breast cancer: Further evidence that these cells matter
Presenter: Bruna Filipa Correia
Session: Poster Display session
Resources:
Abstract
202P - Mining tumor infiltrating B cells to discover antibody-target pairs and develop novel therapies
Presenter: Matthieu Delince
Session: Poster Display session
Resources:
Abstract
203P - Targeting IL-33 reprograms tumor microenvironment and potentiates antitumor response to anti-PD-L1 immunotherapy
Presenter: Xuyao Zhang
Session: Poster Display session
Resources:
Abstract
204P - Deciphering the crosstalk between tumor and circulating immune microenvironment in advanced NSCLC patients undergoing immunotherapy
Presenter: Prisca Tamarozzi
Session: Poster Display session
Resources:
Abstract