Abstract 111P
Background
About one-third of newly diagnosed NSCLC was stage III unresectable and resectable patients (pts). Stage III NSCLC have high heterogeneity. Currently, real-world molecular testing pattern, treatment pattern and the associated survival outcomes are limited.
Methods
This prospective real-world study enrolled untreated stage III NSCLC pts from 28 hospitals in China. Unresectable and resectable pts were studied separately in cohort 1(C1) and cohort 2(C2). The primary endpoint was treatment pattern of C1, secondary endpoints included molecular testing pattern, progression-free survival (PFS), overall survival (OS) of C1 and treatment pattern of C2.
Results
From 2019 July to 2022 February, 486 pts were included, with 379 pts in C1 and 107 pts in C2. Median age was 63 years (range: 25-85), 82.9% were male. The testing/positive rates of EGFR, ALK, and PD-L1 (≥1%) were 20.0%/39.2%, 15.0%/23.3%, and 13.0%/73.0%, respectively. In C1, 201 (53.0%) pts received radiotherapy (RT), among whom 86.1% (173/201) were chemoradiotherapy (CRT), including 63.6% (110/173) concurrent CRT (cCRT) and 36.4% (63/173) sequential CRT (sCRT). Following CRT, 53.8% pts received consolidation therapy, among whom 58.1 % were immunotherapy-based (IO-based) therapy, of with 35.2% were durvalumab-based therapy. For pts without RT, chemotherapy only or chemotherapy plus anti-angiogenesis therapy, was most commonly used (60.1% [107/178]), followed by chemoimmunotherapy (27.0% [48/178]). In C2, 61.9% had neo-adjuvant treatment, with chemotherapy alone (40.0%) or combined with IO (40%) as the main regimens. Adjuvant treatment was planned for 71.4% pts. As of April 30, 2024 (data cut-off), for pts in C1, the overall median PFS (mPFS) and median OS (mOS) were 12.6 months (95% CI, 11.0-14.0) and 33.3 months (95% CI, 29.6-NE), respectively. For pts in C1 treated with CRT followed by IO-based consolidation therapy, mPFS and mOS were 15.1 months (95% CI, 12.7-28.5) and NE (95% CI, 30.5-NE), respectively. The 2-yr OS rate was 82.6% (95%CI, 69.2-90.6).
Conclusions
MOOREA study presents real-world testing and treatment patterns in stage III NSCLC and showed the effectiveness of CRT followed by IO-base consolidation therapy in this setting.
Clinical trial identification
NCT04023812.
Legal entity responsible for the study
AstraZeneca.
Funding
AstraZeneca.
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