Abstract 146P
Background
The CROSS and NEOCRTEC-5010 trials established neoadjuvant chemoradiotherapy (nCRT) as the standard for locally advanced esophageal cancer (EC). The ESCORT-NEO study showed the efficacy and safety of neoadjuvant immunotherapy combined with chemotherapy in locally advanced esophageal squamous cell carcinoma (LA-ESCC). However, reports on the combined approach in adenocarcinoma of the esophagogastric junction (AEG) are lacking. This phase II trial evaluates the efficacy and safety of neoadjuvant adebrelimab with nab-paclitaxel, lobaplatin, and S-1 in resectable locally advanced AEG.
Methods
Treatment-naive patients with cT3-4NanyM0 resectable locally advanced AEG and ECOG PS 0-1 received adebrelimab (1200 mg IV) on Day 1, nab-paclitaxel (180-200 mg IV) on Day 1, lobaplatin (50 mg IV 2h) on Day 1, and S-1 (40 mg, bid po) every 3 weeks for 2 cycles, followed by surgery and investigator's choice of adjuvant treatment. The primary endpoint was the pathologic complete response (pCR) rate; secondary endpoints included R0 resection rate, overall response rate (ORR), event-free survival (EFS), disease-free survival (DFS), safety.
Results
From November 2023 to June 2024, 15 patients were enrolled and completed neoadjuvant treatment; 2 patients were lost to follow-up, and 5 refused surgery. Among the 8 patients who underwent surgery, 1 (12.5%) achieved pCR, and all achieved R0 resection. Tumor regression grades (TRG) observed were TRG0 in 1 (12.5%), TRG2 in 5 (62.5%), and TRG3 in 2 (25.0%) patients. Of the 13 evaluable patients, 8 (62%) achieved partial response (PR) and 5 (38%) had stable disease (SD). ORR and DCR were 62% (8/13) and 100.0% (13/13), respectively. Treatment-related adverse events (TRAEs) occurred in 100% of patients, but no grade 3-5 TRAEs were observed. Toxicity and post-surgery complications were limited, and surgical feasibility was not impacted.
Conclusions
Neoadjuvant adebrelimab combined with chemotherapy, followed by surgery and adjuvant treatment, demonstrated good efficacy and safety in patients with resectable locally advanced AEG, offering a promising treatment option for this patient population.
Clinical trial identification
NCT06198465.
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