Abstract 2204P
Background
Malignant pleural mesothelioma (MPM) is a rare thoracic malignancy with bad prognosis. Asbestos exposure has been described as the main risk factor with a key role in its pathogenesis. The aim of this study is to identify the impact of systemic inflammation biomarkers as clinical prognostic factors for MPM.
Methods
Patients (pts) diagnosed of MPM from 2004 to 2023 from a Medical Oncology Intercenter Unit in Malaga (Spain) were enrolled. We analyzed epidemiologic, clinical and pathological characteristics and correlated them with survival outcomes.
Results
Among the 140 pts, median age was 70 years (range 23-94), ECOG 0-1 in 76,4% (n=104), mainly males (70,7%, n=99). 95 pts (67,9%) were epithelioid subtype. Median follow up was 21,6 months (mo) (range 1-217). Median overall survival (OS) 13,5 mo (CI 95% 9,6-17,4), progression-free survival (PFS) 10,1 mo (CI 95% 7,2-13). 19 pts (13,6%) were considered for surgery. In non-resectable pts (n=121, 86,4%), age over 65, malnutrition and ECOG 2-4 at diagnosis were associated to poor OS (21,6 mo CI95% 14,4-28,8; 7,1 mo, CI95% 5,8-8,2; 4,7 mo, CI95% 3-6,5 respectively). Inflammatory biomarkers including high LDH or CRP, neutrophilia, Lung Immune Prognostic Index (LIPI) intermediate-poor, and high dNLR suggested a trend towards poor survival (9,5 mo CI 95% 3,5-15,4; 8,5 mo CI 95% 4,5-12,5; 7,1 mo CI 95% 1,5-3,9; 9,5 mo CI95% 4,5-14,4; 9,5 mo CI95% 4,8-14, respectively; p>0.5). Anemia, moderate-to-severe value of neutrophil to lymphocyte ratio (NLR≥6) and not receiving immunotherapy were significantly associated with worse prognosis. Multivariate analysis showed age and NLR value as independent prognostic factors (p<0.01).
Conclusions
Host inflammation status at diagnosis may be a subrogate biomarker of survival for MPM, even for pts not receiving immunotherapy. Modulating the immune system and inflammatory pathways appear as promising strategies for increasing effectiveness in MPM treatment. Table: 2204P
Univariate analysis | Multivariate analysis | |||||
HR | CI 95% | P | HR | CI 95% | P | |
Age ≤65 | 0,56 | 0,36-0,88 | 0,01 | 0,44 | 0,23-0,82 | 0,01 |
ECOG | 1,65 | 1,3-2,6 | 0,00 | - | - | 0,37 |
Malnutrition | 0,47 | 0,29-0,74 | 0,00 | - | - | 0,78 |
Anemia | 9,86 | 0,76-0,96 | 0,01 | - | - | 0,29 |
High C reactive protein | 1,87 | 0,77-4,52 | 0,16 | - | - | - |
Neutrophilia | 2,38 | 0,31-18,41 | 0,40 | - | - | - |
High LDH | 1,47 | 0,93-2,34 | 0,09 | - | - | - |
NLR (absent-mild vs moderate severe) | 0,5 | 0,28-0,90 | 0,02 | 0,30 | 0,14-0,61 | 0,00 |
dLNR (high vs normal) | 0,91 | 0,58-1,42 | 0,69 | - | - | - |
LIPI score (good vs intermediate-poor) | 1,47 | 0,96-2,27 | 0,07 | - | - | - |
Immunotherapy | 0,48 | 0,24-0,96 | 0,04 | - | - | 0,62 |
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
2203P - Uncovering prognostic transcriptomic differences in epithelioid malignant pleural mesothelioma
Presenter: Mario Occhipinti
Session: Poster session 07
2205P - Tumor-infiltrating lymphocytes score possesses a relation with adjuvant chemo-immunotherapy benefit and cellular morphology in large-cell neuroendocrine carcinoma
Presenter: Zhiwen Luo
Session: Poster session 07
2207P - Mainstream germline genetic testing in routine oncological care of EGFR mutant non-small cell lung cancer in the United Kingdom
Presenter: Hazel O'Sullivan
Session: Poster session 07
2208P - The single-cell proteomic landscape of pulmonary lymphoepithelioma-like carcinoma
Presenter: Chi Cho
Session: Poster session 07
2209P - Mutational status of non-small cell lung cancer in Portugal: A multicentric study
Presenter: Joana Duarte
Session: Poster session 07
2210P - Reprogramming of pyrimidine metabolism drives tumorigenesis in NF2-deficient malignant pleural mesothelioma
Presenter: Duo Xu
Session: Poster session 07
2234P - Local immune-related adverse events (irAEs) are more common in tumor-bearing organs
Presenter: Steve Blum
Session: Poster session 07
2235P - Chemotherapy priming leads to hypermutability and immune surveillance in colorectal cancer
Presenter: Pietro Paolo Vitiello
Session: Poster session 07
2236P - MHC-II neoantigens and copy number alterations (CNA) drive immune checkpoint inhibitor (ICI) response in metastatic melanoma (MM)
Presenter: Benjamin Shum
Session: Poster session 07