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
88P - Utilisation of the ESMO-MCBS in prioritising immune-checkpoint inhibitors for a WHO model list of essential medicines application
Presenter: Mario Csenar
Session: Poster Display session
Resources:
Abstract
89P - Safety and efficacy of rechallenge with immune checkpoint inhibitors in advanced solid tumor: A systematic review and meta-analysis
Presenter: Huijun Xu
Session: Poster Display session
Resources:
Abstract
90P - Meta-analysis of hypophysitis incidence in melanoma patients treated with immune checkpoint inhibitors
Presenter: Vincas Urbonas
Session: Poster Display session
Resources:
Abstract
91P - Territorial disparities in the use of hospitalization at home for immune checkpoint inhibitors infusion in France between 2021 and 2022
Presenter: Anne Claire Toffart
Session: Poster Display session
Resources:
Abstract
92P - An investigation on the differences between the pre-treatment nutritional and immunological status of nasopharyngeal carcinoma patients and the healthy population
Presenter: Qiao He
Session: Poster Display session
Resources:
Abstract
93P - Pseudoprogression in immunotherapy: Illusion or reality? P-PIT study
Presenter: Amelie Toulet
Session: Poster Display session
Resources:
Abstract
94P - Real-world characteristics, treatments and healthcare recourse utilization (HCRU) of patients (pts) with advanced/metastatic non-small cell lung cancer (mNSCLC) managed with first line (1L) immuno-oncology (IO) strategies in Greece: The IO-HORIZON study
Presenter: Dimitrios Ziogas
Session: Poster Display session
Resources:
Abstract
95P - Quality of life (QoL) and care pathway in patients with durable response to immune checkpoint inhibitors (ICI-DR) for advanced or metastatic non-small cell lung cancer (NSCLC) or melanoma: QUALICI study
Presenter: Nicolas Girard
Session: Poster Display session
Resources:
Abstract
96P - Comparative cardiovascular risks of PD-1 vs. PD-L1 inhibitors: A meta-analysis of incidence and severity of cardiotoxicity
Presenter: Mohammedbaqer Al-Ghuraibawi
Session: Poster Display session
Resources:
Abstract
97P - Cardiac risk stratification and serial monitoring during immune checkpoint inhibitor therapy: Prospective real-world experience
Presenter: James Knott
Session: Poster Display session
Resources:
Abstract