Abstract 109P
Background
BM significantly impacts the prognosis of patients (pts) with NSCLC. For pts without targetable gene mutations, treatment options are limited, and the roles of immunotherapy and brain radiotherapy remain controversial. This study aims to examine the effectiveness of first-line immune-based therapies and brain radiotherapy for these pts using real-world data.
Methods
Thirty-nine pts with BM from NSCLC harboring non-sensitizing mutations in EGFR, ALK, or ROS1 were enrolled. The study evaluated the efficacy of first-line immune-based combination therapy and brain radiotherapy. Additionally, it explored the relationship between PD-L1 expression levels in extracranial tissues and intracranial treatment outcomes.
Results
First-line systemic treatment had two groups: one group received immunotherapy plus chemotherapy (I+C, n=21), while the other group received immunotherapy plus antiangiogenic therapy, with or without chemotherapy (I+A±C, n=18). There was no significant difference in intracranial progression-free survival (icPFS), intracranial overall survival (icOS), progression-free survival (PFS), and overall survival (OS) between the two groups (all p > 0.05). Additionally, whether or not to receive brain radiotherapy had no significant effect on survival outcomes (all p > 0.05). There were no significant differences in the intracranial objective response rate (icORR) and intracranial disease control rate (icDCR) between different first-line treatment groups and between those receiving or not receiving brain radiotherapy (all p > 0.05). Analysis of survival results revealed statistically significant differences in icPFS, icOS, PFS, and OS between the PD-L1 high expression group (≥ 50%) and the low expression group (<50%), with p-values of 0.002, 0.003, 0.029, and 0.003, respectively.
Conclusions
Different first-line immunotherapy combinations had no significant effect on the survival outcomes of pts with driver gene-negative BM NSCLC, and brain radiotherapy did not bring additional survival benefits. The PD-L1 TPS expression level in extracranial tissues appears to be a prominent predictor of the efficacy of intracranial immunotherapy.
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
31P - Peripheral-blood Immune-predictors of pathological complete response in patients with triple-negative breast cancer undergoing neoadjuvant chemo-immunotherapy
Presenter: Celeste Santoro
Session: Poster Display session
Resources:
Abstract
32P - Immune T cell subsets dynamics in the early TNBC treatment setting
Presenter: Rocío Martín Lozano
Session: Poster Display session
Resources:
Abstract
33P - Tumor-specific CD4 Th1 responses in long-term responder melanoma patients treated with immune checkpoint inhibitors.
Presenter: Jessica Mathiot
Session: Poster Display session
Resources:
Abstract
34P - Linking early immunity changes to clinical outcomes in cutaneous squamous cell carcinoma following anti-programmed death cell-1 (PD-1) treatment
Presenter: Marcella Scala
Session: Poster Display session
Resources:
Abstract
36P - Exploring the role of soluble B7-H3 (sB7-H3) as a biomarker to predict the clinical benefit and/or the occurrence of immune related adverse events (irAEs) in advanced cancer patients treated with immune checkpoint inhibitors (ICIs)
Presenter: Luigi Liguori
Session: Poster Display session
Resources:
Abstract
37P - Lymphocyte Subpopulation Balances as a Blood Biomarker for Immune-Related Adverse Events in Patients Receiving Immune Checkpoint Inhibitors
Presenter: Mireille Langouo fontsa
Session: Poster Display session
Resources:
Abstract
38P - Biomarkers predictive of response to immune checkpoint inhibitor therapy in patients with metastatic melanoma
Presenter: Eliza Bob
Session: Poster Display session
Resources:
Abstract
39P - Analysis of the immune response patterns in localized prostate cancer
Presenter: Sara Merler
Session: Poster Display session
Resources:
Abstract
40P - MANIFEST: A Multiomic Profiling Platform for Immuno-Oncology Biomarker Discovery
Presenter: Zayd Tippu
Session: Poster Display session
Resources:
Abstract
41P - Total tumor burden and radiomics to evaluate response in dose escalation studies: Roginolisib (IOA-244), a highly selective PI3Kd inhibitor in metastatic uveal melanoma patients
Presenter: Anna Di Giacomo
Session: Poster Display session
Resources:
Abstract