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Clinical Trials/NCT06341595
NCT06341595
Recruiting
Phase 2

Concurrent Chemoradiotherapy Combined With Sintilimab as Neoadjuvant Therapy for Advanced Gastric Cancer Patients With Para-aortic Lymph Node Metastasis: a Single-arm, Phase II, Exploratory Study.

The First Affiliated Hospital with Nanjing Medical University1 site in 1 country40 target enrollmentApril 1, 2024

Overview

Phase
Phase 2
Intervention
Sintilimab
Conditions
Gastric Cancer
Sponsor
The First Affiliated Hospital with Nanjing Medical University
Enrollment
40
Locations
1
Primary Endpoint
Recurrence free survival (RFS)
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

This trial is a prospective, single arm, single center, phase II clinical study aimed at subjects with advanced gastric cancer and para aortic lymph node metastasis, exploring the feasibility and safety of Sintilimab Injection combined with synchronous chemo-radiotherapy as neoadjuvant therapy.

Patients will receive sintilimab Injection (200mg iv q3w d1) combined with concurrent radiotherapy and chemotherapy. The chemotherapy regimen will use oxaliplatin 130mg/m2+S-1 40mg/m2 bid d1-14. Radiotherapy is performed using intraperitoneal radiation therapy, once a day, five times a week, at a dose of 1.8-2 Gy/f, for a total of 45-50.4 Gy (60-66 Gy for lymph node lesions). Radiation therapy starts from the second cycle of Sintilimab Injection combined with chemotherapy. The subjects underwent imaging evaluation after completing 4 cycles of combination chemotherapy and radiation therapy with Sintilimab Injection. Evaluated as a surgical subject (surgical conditions: imaging evaluation of enlarged lymph nodes adjacent to the abdominal aorta with PR or no significant activity), radical surgery will be performed within 4 weeks after the last study drug treatment. After surgery, the researcher will determine the necessity of adjuvant treatment and develop an adjuvant treatment plan based on the subject's condition. Subjects evaluated as inoperable will have their best follow-up treatment plan determined by the researcher.

Registry
clinicaltrials.gov
Start Date
April 1, 2024
End Date
December 31, 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

combination therapy

sintilimab combined with chemotherapy and radiotherapy

Intervention: Sintilimab

combination therapy

sintilimab combined with chemotherapy and radiotherapy

Intervention: Extraperitoneal radiation therapy

combination therapy

sintilimab combined with chemotherapy and radiotherapy

Intervention: Oxaliplatin

combination therapy

sintilimab combined with chemotherapy and radiotherapy

Intervention: S-1

Outcomes

Primary Outcomes

Recurrence free survival (RFS)

Time Frame: 24 months

Recurrence free survival of patients undergoing surgery after Sintilimab Injection combined with concurrent chemoradiotherapy

Secondary Outcomes

  • Adverse reactions(24 months)
  • Overall survival (OS)(24 months)
  • R0 resection rate(12 months)
  • Major pathological response rate (MPR)(12 months)
  • Objective response rate (ORR)(24 months)

Study Sites (1)

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