Efficacy and Safety of Serplulimab Combined With Chemotherapy as Neoadjuvant Treatment for Locally Advanced Gastric Cancer or Adenocarcinoma of Esophagogastric Junction

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorXijing Hospital

About this trial

This is a multicenter, double-blind, randomized, phase 2 trial to investigate the efficacy and safety of serlulimab combined with nab-paclitaxel plus SOX versus nab-paclitaxel plus SOX alone as neoadjuvant treatment for locally advanced GC or AEG.

The goal of this clinical trial is to learn if serlulimab combined with nab-paclitaxel plus SOX as neoadjuvant treatment for locally advanced AEG/GC. It will also learn about the safety of serlulimab combined with nab-paclitaxel plus SOX. The main questions it aims to answer are:

Does serlulimab increase the pCR of participants with locally advanced AEG/GC ? What medical problems do participants have when taking serlulimab? Researchers will compare to a placebo (a look-alike substance that contains no drug) to see if serlulimab combined with nab-paclitaxel plus SOX as neoadjuvant treatment for locally advanced AEG/GC.

Participants will:

Eligible patients were randomly assigned to receive serlulimab (4.5 mg intravenously on day 1) combined with chemotherapy (nap-paclitaxel 260 mg/m2 intravenously on days 1, OXA 130mg/ /m2, intravenously on days 1, and S-1 40 to 60 mg orally twice daily depending on BSA on days 1 to 14) or chemotherapy alone every 3 weeks for 3 preoperative cycles followed by 3 postoperative cycles. All patients will be followed for survival.

Eligibility criteria

Qualifiers

Age older than 18 and younger than 75 years

Primary GC or AEG (Siewert II/III)confirmed pathologically by endoscopic biopsy

Clinical stage T3/T4N+M0 disease as assessed by CT/MRI, PET-CT, and laparoscopy, if feasible

At least one measurable lesion according to the RECIST, version 1.1

Disqualifiers

Squamous cell carcinoma, adenosquamous cell carcinoma, small cell carcinoma, and undifferentiated gastric cancer were confirmed by pathology

Positive Her-2 detection (IHC3+ or IHC2+ amplified by FISH detection)

Prior chemotherapy, radiotherapy, hormone therapy, targeted therapy, or immunotherapy

Contraindications for surgical treatment or chemotherapy

Trial design

Treatments tested in this trial

  • Serplulimab Combined With Chemotherapy
  • Placebo combined with Chemotherapy

Treatment groups

116 Participants
are divided into 2 treatment groups

Locations

5
The fourth hospital of Hebei Medical University050000, ShijiazhuangHeibei Province, China
Department of Digestive surgery, Xijing Hospital of Digestive Diseases, Air Force Medical University, Xi' an, China710032, Xi'anShaanxi, China
Department of General Surgery, Tangdu Hospital, Air Force Medical University710032, Xi'anShaanxi, China
Department of General Surgery, The 986th Military Hospital, Air Force Medical University710032, Xi'anShaanxi, China

Sponsors and collaborators

Xijing Hospital

Lead sponsor

Tang-Du Hospital

Collaborator

Hebei Medical University Fourth Hospital

Collaborator

Tianjin Medical University Cancer Institute and Hospital

Collaborator