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
43P - Machine learning radiomics based on CT to predict response to lenvatinib plus tislelizumab based therapy for unresectable hepatocellular carcinoma
Presenter: Gang Chen
Session: Poster Display session
Resources:
Abstract
44P - Machine learning-based prediction of survival in patients with metastatic renal cell carcinoma receiving first-line immunotherapy
Presenter: Ahmed Elgebaly
Session: Poster Display session
Resources:
Abstract
45P - Gut microbiome signatures for exploring the correlation between gut microbiome and immune therapy response using machine learning approach
Presenter: Han Li
Session: Poster Display session
Resources:
Abstract
46P - Abnormal gut microbiota may cause PD-1 inhibitor-related cardiotoxicity via suppressing regulatory T cells
Presenter: Zeeshan Afzal
Session: Poster Display session
Resources:
Abstract
47P - Correlation of clinical, genetic and transcriptomic traits with PD-L1 positivity in TNBC patients
Presenter: Anita Semertzidou
Session: Poster Display session
Resources:
Abstract
48P - The A2AR antagonist inupadenant promotes humoral responses in preclinical models
Presenter: Paola Tieppo
Session: Poster Display session
Resources:
Abstract
49P - Highly potent novel armoured IL13Ra2 CAR T cell targeting glioblastoma
Presenter: Maurizio Mangolini
Session: Poster Display session
Resources:
Abstract
50P - Phase I trial of P-MUC1C-ALLO1 allogeneic CAR-T cells in advanced epithelial malignancies
Presenter: David Oh
Session: Poster Display session
Resources:
Abstract
51P - Unlocking CAR-T cell potential: Lipid metabolites in overcoming exhaustion in ovarian cancer
Presenter: Xiangyu Chang
Session: Poster Display session
Resources:
Abstract
52P - Tumor-targeted cytokine release by genetically-engineered myeloid cells rescues CAR-T activity and engages endogenous T cells against high-grade glioma in mouse models
Presenter: Federico Rossari
Session: Poster Display session
Resources:
Abstract