Abstract 92P
Background
The relative lymphocyte count (RLC) is a simple and widely available host-related biomarker. RLC is explored as a potential marker of immune checkpoint inhibitor therapy outcomes in patients with non-small-cell lung cancer (NSCLC). The objective of this study was to investigate the predictive value of RLC reduction for occurrence of serious immune-related adverse events (sirAEs) in patients with metastatic NSCLC, treated in the clinic of Medical oncology of Military Medical Academy in Sofia, Bulgaria.
Methods
The information was obtained retrospectively from the medical documentation of the pts with metastatic NSCLC, treated with immunotherapy (mono or in a combination with chemotherapy) in our institution in the period from m.05.2018 to m.05.2023. Descriptive statistical analysis was used. The RLC is measured at the onset of treatment and compared with the RLC at the time of diagnosis of irAEs. For the pts without irAEs the comparison is made between the initial RLC, normal or abnormal, and the occurrence of reduction in RLC during the course of treatment. As a reduction in RLC is defined as the drop of the lymphocyte count with more than 50% of the initial value if the lower RLC value is under 20% of the WBC.
Results
Thirty four pts with metastatic NSCLC were treated with immunotherapy (first, second or consecutive line) in our institution during the last 5 years. 3/34 (9%) were diagnosed with grade 1 or 2 irAEs, 5/34 (15%) with sirAEs (grade 3 to 5). In 4/5 (80%) of the cases with sirAEs we observed a reduction in RLC. 0/3 (0%) of the pts with grade 1 or 2 irAEs and 9/26 (35%) of the pts without immune-related toxicities met the criteria for RLC reduction. The pts with sirAEs had significantly higher RLC reduction rate than the pts with low grade or without immune-related toxicities. The χ2 statistic was 8.6595, leading to a p-value of 0.03745.
Conclusions
Our data suggest that RLC reduction is a strong predictive biomarker for sirAEs (p<0.05). The underlying pathophysiologic mechanism of this observation remains to be determined.
Editorial acknowledgement
N/A
Clinical trial identification
N/A
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
20P - Effects of <italic>Apis dorsata</italic> honey on the expression of selected CYP450, pro-apoptotic, and anti-apoptotic genes during induced cytotoxicity in cyclophosphamide-treated human lung carcinoma (A549) cells
Presenter: Jose Kenneth Narag
Session: Cocktail & Poster Display session
Resources:
Abstract
21P - Hsa_circ_0009061 inhibits the progression of bladder cancer through the miR-889-3p/CPEB3 axis
Presenter: Minkang Wu
Session: Cocktail & Poster Display session
Resources:
Abstract
22P - Exploring exportin-1 as a therapeutic vulnerability in lung squamous cell carcinoma
Presenter: Vidushi Durani
Session: Cocktail & Poster Display session
Resources:
Abstract
23P - Identification of HPSE as potential novel therapeutic target for lung adenocarcinoma patients
Presenter: Samuel Doré
Session: Cocktail & Poster Display session
Resources:
Abstract
24P - High-throughput plasma proteomics profiling in early breast cancer
Presenter: Isabella Lombardo
Session: Cocktail & Poster Display session
Resources:
Abstract
25P - Immunohistochemical analysis of ROR1 and BMI-1 expression in luminal breast cancer
Presenter: Sergey Vtorushin
Session: Cocktail & Poster Display session
Resources:
Abstract
26P - Associations between cancer stem cells (CSC) markers and androgen (AR) and estrogen (ER) receptors expression in prostate cancer (PCa)
Presenter: Marina Puchinskaya
Session: Cocktail & Poster Display session
Resources:
Abstract
27P - Proteomic profiling reveals organ-specific differences in metastases and identifies potential biomarkers for recurrence risk in localized colon cancer
Presenter: Blanca García-Micó
Session: Cocktail & Poster Display session
Resources:
Abstract
28P - Collagen-activated signalling pathway is significantly hypermethylated in high-grade serous ovarian cancer (HGSOC) patients treated with platinum-containing neoadjuvant chemotherapy (NACT)
Presenter: Jose Alejandro Perez Fidalgo
Session: Cocktail & Poster Display session
Resources:
Abstract
29P - Quantitative tissue analysis reveal adenylate kinase 2 protein signatures: Therapeutic target for meningioma
Presenter: Rashmi Rana
Session: Cocktail & Poster Display session
Resources:
Abstract