S-1 and Oxaliplatin (SOX) Plus Sintilimab in the Locally Advanced Esophagogastric Junction Adenocarcinoma

NCT04989985 | Recruiting Phase 2

• 1 other identifier: SOLAR
• Study Type: interventional
• Target: 302
• Locations: 1 country
• Sites: 1

Brief Summary

For locally advanced adenocarcinoma of esophagogastric junction(AEG) (cT3-4aN+M0), neoadjuvant chemotherapy was improved to downstage T and N stage, increase the resectability of tumor, and finally improve the long-term survival. Combination of perioperative PD-1 antibody and chemotherapy for locally advanced AEG could be a novel therapy to increase response rate and resectability and reduce recurrence rate. Sintilimab in this study is an anti-PD-1 monoclonal antibody for injection which has been approved for several malignant tumors. This study is a multi-center, open-label, randomized phase II clinical trial to evaluate tolerability, safety and efficacy of sintilimab in combination with perioperative chemotherapy in locally advanced AEG.

Conditions

Locally Advanced Gastroesophageal Junction Adenocarcinoma; Chemotherapy Effect

Keywords

Locally Advanced Gastroesophageal Junction Adenocarcinoma; sinitilimab; SOX; peri-operative chemotherapy

Outcome Measures

Primary Outcomes (1)

• pCR

  pathological complete response rate

  From the initiation date of first cycle (each cycle is 21 days) to the date of operation, an average of 12 weeks.

Secondary Outcomes (5)

• TRG0/1

  From the initiation date of first cycle (each cycle is 21 days) to the date of operation, an average of 12 weeks.

• R0 resection rate

  rom the initiation date of first cycle (each cycle is 21 days) to the date of operation, an average of 12 weeks.

• DFS

  From the initiation date of first cycle (each cycle is 21 days) to the date of first documented symptoms of cancer, assessed up to 3 years

• RFS

  From the initiation date of first cycle (each cycle is 21 days) to the date of first documented progression or date of death from any cause, whichever came first, assessed up to 3 years

• OS

  From the initiation date of first cycle (each cycle is 21 days) to the date of death from any cause, whichever came first, assessed up to 5 years

Study Arms (2)

Active Comparator

ACTIVE COMPARATOR

SOX: Oxaliplatin+S-1 Oxaliplatin: 130mg/m2, iv drip for 2h, d1, q3w; S-1:40\~60mg Bid, d1\~14, q3w; Neoadjuvant chemotherapy for 2-4 cycles, adjuvant chemotherapy for 4-6 cycles.

Drug: Oxaliplatin+S-1

Experimental

EXPERIMENTAL

Sinitlimab + SOX； SOX: Oxaliplatin+S-1 Sinitlimab: 200mg, ivdrip, d1, q3w; Oxaliplatin: 130mg/m2, iv drip for 2h, d1, q3w; S-1:40\~60mg Bid, d1\~14, q3w; Neoadjuvant chemotherapy for 2-4 cycles, adjuvant chemotherapy for 4-6 cycles.

Drug: Sinitilimab+oxaliplatin+S-1

Interventions

Oxaliplatin+S-1 DRUG

Drug: Oxaliplatin Oxaliplatin: 130mg/m2，iv drip for 2h，d1, q3w Drug: S-1 S-1: 40\~60mg Bid，d1\~14, q3w

Also known as: SOX

Active Comparator

Sinitilimab+oxaliplatin+S-1 DRUG

Drug: Sintilimab Sintilimab, recombinant humanized anti-PD-1 monoclonal antibody for injection; 200mg ivdrip, d1, q3w. Other Name: PD-1 antibody Drug: Oxaliplatin Oxaliplatin: 130mg/m2，iv drip for 2h，d1, q3w Drug: S-1 S-1: 40\~60mg Bid，d1\~14, q3w

Also known as: Sinitilimab+SOX

Experimental

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Written (signed) informed consent;
• Histologically CT/MRI confirmed cT3-4aN+M0 Esophagogastric Junction Adenocarcinoma;
• Consent to send tumor tissue from biopsy or resection for PD-L1, EBV, MSI detection;
• Female or male, 18-75 years;
• ECOG 0-1, no surgery contraindications;
• Physical condition and adequate organ function to ensure the success of abdominal and/or thoracic surgery;
• Expected survival ≥ 6 months;
• Adequate hematological, liver, renal and coagulation function; 1) Platelet (PLT) count ≥100,000 /mm3; 2) White Blood cell（WBC）count ≥4,000 /mm3 and ≤15,000 /mm3 ；Neutrophil count (ANC) ≥1,500 /mm3; 3) Hemoglobin (Hb) level ≥9.0 g/dl; 4) International normalized ratio (INR) ≤1.5; 5) Prothrombin time (PT) and activated partial thromboplastin time (APTT) ≤1.5×ULN; 6) Glycosylated hemoglobin (HbA1c) \<7.5%; 7) Total bilirubin (TBIL) level ≤1.5×ULN; 8) Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) level ≤2.5×ULN (≤5×ULN in case of liver metastasis); 9) Alkaline phosphatase level ≤2.5×ULN (≤5×ULN in case of liver metastasis); 10) Serum creatinine (Cr) level ≤1.5×ULN and creatinine clearance ≥60 ml/min;
• Patients with Good compliance, who can cooperate with the laboratory, auxiliary examinations and corresponding specimen collection of this program set;
• Females of child bearing age must have a negative pregnancy test, and have to take contraception measures and avoid breast feeding during the study and for 6 months after the last dose; male subjects must agree to taken contraception measures during the study and for 6 months after the last dose.

You may not qualify if:

• Suffer from other active malignant tumors within 5 years or at the same time. Cured localized tumors, such as skin basal cell carcinoma, skin squamous cell carcinoma, superficial bladder cancer, prostate carcinoma in situ, cervical carcinoma in situ, breast carcinoma in situ, etc. can be included in the group.
• Patients who are planning to undergo or have previously received organ or bone marrow transplantation.
• Myocardial infarction or poorly controlled arrhythmia (including QTc interval ≥ 450 ms for males and ≥ 470 ms for females) occurred within 6 months before the first medication (QTc interval is calculated by Fridericia's formula).
• There is NYHA standard grade III to IV cardiac insufficiency or color Doppler ultrasound examination: LVEF (left ventricular ejection fraction) \<50%.
• Human immunodeficiency virus (HIV) infection.
• Suffer from active tuberculosis.
• Past and present patients who have interstitial pneumonia, pneumoconiosis, radiation pneumonia, drug-related pneumonia, severely impaired lung function, etc., which may interfere with the detection and management of suspected drug-related lung toxicity.
• There is a known active or suspicious autoimmune disease. Except those who were in a stable state of the disease at the time of enrollment (no need for systemic immunosuppressive therapy).
• Received treatment with live vaccine within 28 days before the first administration; except for the treatment of seasonal influenza with inactivated viral vaccine.
• Patients who need to receive systemic corticosteroids (\> 10 mg/day curative dose of prednisone) or other immunosuppressive drugs within 14 days before the first medication or during the study period. However, the following conditions are allowed to enter the group: in the absence of active autoimmune diseases, patients are allowed to use topical or inhaled steroids, or adrenal hormone replacement therapy with a dose of ≤ 10 mg/day prednisone.
• Any active infection that requires systemic anti-infective treatment occurs within 14 days before the first administration of the drug; except for receiving preventive antibiotic treatment (such as prevention of urinary tract infection or chronic obstructive pulmonary disease).
• Have received other antibody/drug treatments for immune checkpoints in the past, such as PD-1, PD-L1, CTLA4 and other treatments.
• Are receiving other clinical research treatments, or the planned start of this research treatment is less than 14 days from the end of the previous clinical research treatment.
• Known to have a history of severe allergies to any monoclonal antibodies or study drug excipients.
• Known history of psychotropic drug abuse or drug use; patients who have stopped drinking can be included in the group.

Sponsors & Collaborators

• Sixth Affiliated Hospital, Sun Yat-sen University: lead
• Sun Yat-sen University: collaborator

Study Sites (1)

The sixth affiliated hospital of Sun Yat-sen University

Guangzhou, Guangdong, 510060, China

RECRUITING

Study Officials

• Jun-Sheng Peng, Dr

  Sixth Affiliated Hospital, Sun Yat-sen University

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Jun-Sheng Peng

CONTACT

+8613802963578; pengjsh@mail.sysu.edu.cn

Shi Chen

CONTACT

13828496699; chensh47@mail.sysu.edu.cn

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Chief, professor

Study Record Dates

• First Submitted: June 16, 2021
• First Posted: August 4, 2021
• Study Start: September 1, 2021
• Primary Completion: August 1, 2024
• Study Completion (Estimated): August 1, 2027
• Last Updated: August 4, 2021

Record last verified: 2021-07

Locations

CN (1)