RecruitingPhase 2NCT05033392

PD-1 Blockade With JS001 Plus Neoadjuvant Chemotherapy for Gastric/Gastroesophageal Junction Cancer

An Open, Single-center, Phase II Clinical Trial Evaluating the Efficacy of PD-1 Antibody (JS001) in Combination With Neoadjuvant Chemotherapy for Gastric/Gastroesophageal Junction Cancer


Sponsor

Wan He

Enrollment

62 participants

Start Date

Sep 14, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

Gastric cancer (GC),including cardia and noncardia gastric cancer, is responsible for over 480,000 new cases in 2020 and an estimated 370,000 deaths, making it the third most frequently diagnosed cancer and the third leading cause of cancer death in China. Majority of patients(63%) are presented with locally advanced gastric cancer (stage Ⅱ/Ⅲ) and the prognosis is poor. Previous studies have shown that patients with pathological complete response(pCR) following neoadjuvant therapy have longer survival. In 2019, Lancet Oncology published the FLOT4-AIO study which testified that perioperative chemotherapy with FLOT (5-FU/LV, oxaliplatin and docetaxel) regimen has improved pCR rate and prolonged progression free survival(PFS) and overall survival(OS) in patients with stage II/III gastric cancer. Moreover, PD-1 blockade such as nivolumab or pembrolizumab in combination with chemotherapy has shown higher objective response rate(ORR) as compared to chemotherapy alone in advanced gastric cancer. The nanoparticle albumin-bound paclitaxel has been recommended as the second-line chemotherapy for unresectable or recurrent gastric cancer based on the Chinese Society of Clinical Oncology(CSCO) guideline. When PD-1 antibody is applied, albumin-bound paclitaxel is considered as a better partner since no pretreatment of corticosteroids is needed. Thus, the investigators plan to conduct a phase II clinical trial to evaluate the efficacy and safety of toripalimab (PD-1 antibody) combined with the FLOAP (albumin-bound paclitaxel, oxaliplatin, fluorouracil and leucovorin) regimen as the perioperative treatment of cT2-4 and/or N+ GC. The primary end point is pCR rate. The secondary end points include disease free survival(DFS), OS, ORR, R0 resection rate, incidence of adverse events(AE).


Eligibility

Min Age: 18 YearsMax Age: 79 Years

Plain Language Summary

Simplified for easier understanding

This Chinese trial tests adding an immunotherapy drug (JS001, a PD-1 blocker similar to pembrolizumab) to standard chemotherapy before surgery for stomach cancer or cancer of the junction between the stomach and esophagus. The goal is to shrink the tumor before removal and potentially improve long-term survival. **You may be eligible if...** - You are 18–79 years old - You have stomach or gastroesophageal junction cancer confirmed by biopsy - Your cancer is locally advanced (specific staging criteria met) but has not spread to other organs - You are in good overall health (ECOG 0–1) with adequate blood counts and organ function - Tumor tissue is available for biomarker testing (such as PD-L1 status) **You may NOT be eligible if...** - You have received prior treatment for this cancer - Your cancer has spread to distant organs (metastatic) - Your blood counts or organ function do not meet requirements - You have a history of severe immune-related conditions or prior immunotherapy 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

DRUGToripalimab Injection

A domestic PD-1 antibody


Locations(2)

Shenzhen People's Hospital

Shenzhen, Guangdong, China

Shenzhen People's Hospital

Shenzhen, Guangdong, China

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NCT05033392


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