Sintilimab Combined With LDRT for Neoadjuvant Treatment of Locally Advanced dMMR/MSI-H Gastric Cancer

NCT ID: NCT06426654

Last Updated: 2024-05-23

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 45 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-06-10
• Study Completion Date: 2027-08-30

Brief Summary

Recently, growing evidences have suggested that immunotherapy represents a promising treatment option for the neoadjuvant treatment of locally advanced mismatch repair-deficient (dMMR)/microsatellite instability-high (MSI-H) gastric cancer. In this study, we will explore the efficacy and safety of sintilimab and LDRT in the neoadjuvant treatment for locally advanced dMMR/MSI-H G/GEJ cancer.

Detailed Description

This is a prospective, multicenter, single-arm, phase Ib/II trial. In the phase Ib, 4 cases will be enrolled in each treatment group. In the phase II study, a total of 33 patients will be enrolled. Eligible patients will be registered and receive four cycles of sintilimab. Simultaneously, LDRT will be planned and administered. Radical D2 gastric cancer resection will be performed 4-6 weeks after the last administration of sintilimab. The primary endpoint of phase Ib is to determine the optimal radiation dose for phase II study. The primary endpoint of phase II is the pathological complete response (pCR) rate. Secondary endpoints include R0 resection rate, major pathological response (MPR), objective response rate (ORR), 3-year event-free survival (EFS) rate, 3-year overall survival (OS) rate and safety profile of the neoadjuvant regimen.

Conditions

Gastric Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

sintilimab+LDRT

Laparoscopic exploration is required in all patients to detect occult peritoneal metastases.

All patients will start with one cycle of neoadjuvant therapy of sintilimab: 200 mg, iv drip, d1, q3w.

Then, LDRT will be performed in the target area (including the primary gastric lesion and positive/suspected positive lymph nodes).

After radiotherapy, patients will receive another three cycles of sintilimab. Radical D2 gastric cancer resection will be performed 4-6 weeks after the last administration of sintilimab.

The adjuvant therapy will start in 4-6 weeks after the surgery, and we recommend adjuvant treatment with sintilimab for up to 10 cycles.

Group Type: EXPERIMENTAL

sintiliman plus LDRT

Intervention Type: DRUG

All patients will start with one cycle of neoadjuvant therapy of sintilimab: sintilimab 200 mg, iv drip, d1, q3w.

LDRT will be performed in the target area. After radiotherapy, patients will receive another three cycles of sintilimab.

Radical D2 gastric cancer resection will be performed 4-6 weeks after the last administration of sintilimab.

The adjuvant therapy will start in 4-6 weeks after the surgery, and we recommend adjuvant treatment with sintilimab for up to 10 cycles.

Interventions

sintiliman plus LDRT

All patients will start with one cycle of neoadjuvant therapy of sintilimab: sintilimab 200 mg, iv drip, d1, q3w.

LDRT will be performed in the target area. After radiotherapy, patients will receive another three cycles of sintilimab.

Radical D2 gastric cancer resection will be performed 4-6 weeks after the last administration of sintilimab.

The adjuvant therapy will start in 4-6 weeks after the surgery, and we recommend adjuvant treatment with sintilimab for up to 10 cycles.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Age 18-80 years.

2. Histologically or cytologically confirmed diagnosis of locally advanced G/GEJ adenocarcinoma (cT2N+M0 or cT3-4aNanyM0) as assessed by exploratory laparoscopic surgery, ultrasonography and/or CT/MRI.

3. Resectable G/GEJ cancer, as judged by experienced surgeons.

4. dMMR and/or MSI-H.

4. Eastern Cooperative Oncology Group performance score (ECOG PS) ≤1. 5. Agree to provide blood, feces, and tissue specimens. 6. The expected survival is longer than 6 months. 7. There was no previous antitumor treatment (including chemotherapy, radiotherapy, targeted therapy, immunotherapy, interventional therapy, and other treatments with antitumor effects).

8. Adequate organ and hematological function. 9. Strict contraception. 10. Patients must be able to understand and be willing to sign the written informed consent form. A signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure.

Exclusion Criteria

1. Unable to comply with the research program or procedures.

2. Undergoing other drug clinical trials or having participated in any drug clinical trials one month before enrollment.

3. Active autoimmune disease or history of refractory autoimmune disease.

4. Receiving corticosteroids (> 10mg/d prednisone or equivalent dose of steroids) or other systematic immunosuppression therapies within 14 days before enrollment, excluding the following therapies: steroid hormone replacement therapy (≤10mg/d); local steroid therapy; and short-term, prophylactic steroid therapy for preventing allergies or nausea and vomiting.

5. Active or clinically significant cardiac disease:

1. Congestive heart failure > New York Heart Association (NYHA) class 2;

2. Active coronary artery disease;

3. Arrhythmias requiring treatment other than β-blockers or digoxin;

4. Unstable angina (with angina symptoms at rest), new angina within 3 months before enrollment, or new myocardial infarction within 6 months before enrollment

6. Other tumors that have not been treated or exist at the same time, except carcinoma in situ of the cervix, treated basal cell carcinoma or superficial bladder tumor. If the tumor was cured and no evidence of disease was found for more than 3 years, the patient can be enrolled. All other tumors must be treated at least 3 years before enrollment.

7. Patients with a history of HIV infection or active hepatitis B/C.

8. Ongoing > level 2 infection.

9. Symptomatic brain metastasis or meningioma.

10. Unhealed wounds, ulcers or fractures.

11. Renal failure patients requiring blood or peritoneal dialysis.

12. Epileptic that needs medication.

13. Active, symptomatic interstitial pneumonia, pleural or ascites that causes dyspnea (dyspnea ≥ 2 grade).

14. History of organ transplantation (including corneal transplantation).

15. Allergic to research drugs or similar drugs, or suspected allergies.

16. Pregnant or lactating women.

17. The investigator believes that patients who are not suitable for the study.

18. Medical, psychological or social conditions can affect the recruitment of patients and evaluation of study results.

19. Other antitumor therapy (chemotherapy, radiotherapy, surgery, immunotherapy, biotherapy, chemoembolization) other than investigator drugs. Palliative external irradiation for non-target lesions is allowed.

20. Previously used similar immune checkpoint inhibitors.

21. Major surgery 4 weeks before recruitment, open biopsy or major trauma surgery (excluding biliary stents, or percutaneous biliary drainage).

22. Treatment with antitumor Chinese herbal medicine.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

West China Hospital

OTHER

Sponsor Role: lead

Responsible Party

Ming Liu

Clinical Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Kun Yang, M.D.

Role: PRINCIPAL_INVESTIGATOR

West China Hospital

Central Contacts

Pengfei Zhang, M.D

Role: CONTACT

fly_121988@126.com

+86-17828163584

Ming Liu, M.D.

Role: CONTACT

mingliu721@aliyun.com

+86-18980606324

Other Identifiers

WCH242145

Identifier Type: -

Identifier Source: org_study_id