About this trial

Neoadjuvant chemoimmunotherapy for locally advanced gastric and gastroesophageal junction (G/GEJ) cancer is currently under investigation. Most clinical studies have simply combined chemotherapy with anti-PD-1 therapy without considering the impact of chemotherapy drugs on activated immune cells. We designed this study to explore two different treatment regimens for neoadjuvant chemotherapy in patients with locally advanced G/GEJ cancer. One group received FLOT plus toripalimab on Day 1 of each cycle, every 2 weeks for 4 cycles, followed by surgery; the other group received FLOT plus toripalimab on Day 3 of each cycle, every 3 weeks for 3 cycles, followed by surgery. A total of 69 subjects were enrolled. Preliminary statistical analysis conducted one year after the last subject was enrolled revealed no statistically significant differences in pCR and MPR between the two regimens. The median DFS for both groups has not been reached, and there is no statistically significant difference in DFS between the two groups at present. Further subgroup analysis indicated that among subjects with PD-L1 CPS ≥1, the triweekly group achieved a rate of 42.1%, compared to 29.4% in the biweekly group, with no statistically significant difference between the two groups. However, the incidence of bone marrow suppression was lower in the triweekly group than in the biweekly group. Based on the preliminary findings, we plan to conduct an expanded study and transition to a multicenter clinical trial. This study aims to further validate the efficacy of the triweekly chemoimmunotherapy in patients with PD-L1 CPS ≥1 locally advanced G/GEJ cancer.

Eligibility criteria

Qualifiers

70 ≥ Age ≥ 18 years regardless of gender

Gastric adenocarcinoma confirmed by pathology

no distant metastasis and resectable or potentially resectable evaluated by general surgery experts

ECOG PS 0-1

Disqualifiers

Pregnant or lactating women

Suffered from severe infectious diseases within 4 weeks before entering the group

Bronchial asthma requires intermittent use of bronchodilators or medical intervention

Due to the use of immunosuppressants before coexisting diseases and the dosage of immunosuppressants ≥ 10mg/, the oral dose of prednisone lasted for more than 2 weeks

Trial design

Treatments tested in this trial

  • FLOT combined with toripalimab

Treatment groups

60 Participants
are divided into 1 treatment group

Locations

1
Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital450008, ZhengzhouHenan, China

Sponsors and collaborators

Henan Cancer Hospital

Lead sponsor