RecruitingNCT06662110

IMmune Proteomics to Predict neoAdjuvant Chemotherapy and immunoTherapy Response in Gastric Cancer

A Prospective Cohort Study on Serum Immune Protein Signature for Predicting Neoadjuvant Therapy Efficacy in Advanced Gastric Cancer


Sponsor

Shanghai Zhongshan Hospital

Enrollment

206 participants

Start Date

Aug 1, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

The overall efficacy of neoadjuvant treatment for advanced gastric cancer is limited due to significant heterogeneity in patient responses. While neoadjuvant therapy offers hope for improved clinical outcomes, the key challenge is accurately predicting individual treatment responses. Identifying reliable biomarkers to guide treatment decisions is therefore critical. Immune factors are pivotal in the efficacy of gastric cancer treatment, but most research has predominantly focused on the tumor immune microenvironment. This study aims to validate the predictive value of systemic immune markers in predicting neoadjuvant treatment responses in advanced gastric cancer. Building on our previous research, where we established a retrospective cohort of patients with advanced gastric cancer undergoing preoperative chemotherapy, we employed a novel serum proteomics platform based on proximity extension assays (PEA) to measure key immune protein levels in patient serum. This led to the development of the PSRscore system, a serum immune protein score that effectively predicted tumor regression after preoperative chemotherapy (published in Cell Reports Medicine, doi: 10.1016/j.xcrm.2023.100931). In this prospective cohort study, we will enroll 166 patients with resectable advanced gastric cancer undergoing neoadjuvant chemotherapy. Baseline serum samples will be collected prior to treatment, and the PSRscore will be used to predict tumor regression. Pathological evaluation post-chemotherapy will confirm tumor response, helping to further validate and refine the PSRscore system. Additionally, an exploratory cohort of 40 patients receiving combined neoadjuvant chemotherapy and immunotherapy will be included to evaluate the correlation between PSRscore and clinical benefit from immunotherapy. This research is expected to lead to the development of a predictive diagnostic kit based on the PSRscore for advanced gastric cancer patients undergoing neoadjuvant therapy, with the ultimate goal of improving clinical decision-making and enhancing treatment outcomes for gastric cancer patients.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study is looking at whether detailed protein analysis of tumor samples can predict how well chemotherapy — with or without immunotherapy — works before surgery in patients with locally advanced stomach cancer or cancer at the junction of the stomach and esophagus. **You may be eligible if...** - You are between 18 and 75 years old - You have been newly diagnosed with stomach cancer confirmed by a tissue biopsy - Your cancer is locally advanced (stage T3-T4, no distant spread) and is potentially removable with surgery after treatment - You have been recommended for chemotherapy (fluoropyrimidine plus platinum-based drugs), with or without an immune checkpoint inhibitor **You may NOT be eligible if...** - You have already received any cancer treatment for this diagnosis, or any cancer drug within the past 4 weeks - You have a second cancer at the same time - You have a serious medical condition expected to shorten your life to less than 5 years - You have had a blood transfusion in the past week - You have received steroids or immune-suppressing drugs in the past 2 weeks - You received a live vaccine in the past 4 weeks Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTPSRscore

PSRscore calculated based on baseline serum immune proteomics


Locations(1)

Zhongshan Hospital, Fudan University

Xuhui District, Shanghai Municipality, China

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NCT06662110


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