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Toripalimab Combined With FLOT Neoadjuvant Chemotherapy in Patients With Resectable Gastric Cancer

Primary Purpose

Gastric Cancer

Status
Recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Toripalimab
Docetaxel
Fluorouracil
Leucovorin
Oxaliplatin
Sponsored by
Tianjin Medical University Cancer Institute and Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastric Cancer focused on measuring Gastric Cancer, Neoadjuvant Chemotherapy, Immunotherapy, Toripalimab, Pathological Remission

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. locally advanced (>T1) and/or nodal positive (N+) histologically proven adenocarcinoma of the gastric or gastroesophageal junction without distant metastases (M0)
  2. no previous surgical resection
  3. no previous cytostatic chemotherapy
  4. Age > 18 years, no more than 75 years (female and male)
  5. Karnofsky Performance Status score of physical condition is 80-100
  6. surgical resectability
  7. Exclusion of peritoneal carcinomatosis (if clinically suspected) via laparoscopy
  8. Leucocytes > 4.000/µl
  9. Platelets > 100.000/µl
  10. Serum creatinin ≤ 1.5x of normal value, or Creatinin-Clearance > 50 ml/min
  11. written informed consent.

Exclusion Criteria:

  1. Distant metastasis or local invasion of adjacent organs;
  2. Recurrent or residual gastric cancer;
  3. Having or having had autoimmune disease;
  4. Previous organ transplantation or HIV patients;
  5. Allergy or contraindications to Toripalimab, 5- Fluorouracil, Leucovorin, Oxaliplatin, and Docetaxel;
  6. Malignant secondary disease;
  7. Severe non-surgical disease or acute infection;
  8. Peripheral polyneuropathy > NCI grad I;
  9. Blood system, liver and kidney function were damaged;
  10. Symptomatic brain metastasis;
  11. Obvious arrhythmia, myocardial ischemia, severe atrioventricular block, cardiac insufficiency and severe gravity valve disease;
  12. Psychotic subjects who are not easy to control;
  13. Pregnant or lactating subjects.

Sites / Locations

  • Tianjin Medical University Cancer Institute & HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Toripalimab combined with FLOT

Arm Description

In the perioperative period, patients with resectable gastric cancer is treated with flot regimen combined with Toripalimab to observe whether the 3-year disease-free survival (DFS) rate, pathological remission rate, R0 resection rate, D2 radical resection rate, 5-year DFS rate and 5-year OS rate could be improved.

Outcomes

Primary Outcome Measures

3-year Disease-Free Survival Rate
The primary end point of the study is the effect of perioperative time flot regimen combined with Toripalimab and D2 radical operation on the 3-year disease-free survival time of resectable gastric cancer.
Pathological complete response rate (pCR)
Proportion of patients with gastric cancer who received Toripalimab combined with FLOT regimen after 4 cycles of neoadjuvant therapy and postoperative pathological examination TRG1a

Secondary Outcome Measures

Major pathological (complete and nearly complete) response (MPR)
Proportion of patients with gastric cancer who received Toripalimab combined with FLOT regimen after 4 cycles of neoadjuvant therapy and postoperative pathological examination TRG1a or 1b.
Adverse Events
For any adverse reactions, the researchers refer to the National Cancer Institute (NCI) standard of common toxicity (CTC)
5-year Disease-Free Rate
The proportion of patients with resectable gastric cancer who have no recurrence or metastasis after 5 years of perioperative treatment
5-year Survival Rate
Proportion of patients with resectable gastric cancer who survived 5 years after perioperative treatment

Full Information

First Posted
April 15, 2020
Last Updated
February 16, 2021
Sponsor
Tianjin Medical University Cancer Institute and Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04354662
Brief Title
Toripalimab Combined With FLOT Neoadjuvant Chemotherapy in Patients With Resectable Gastric Cancer
Official Title
Phase II Study of Toripalimab Combined With Fluorouracil, Leucovorin, Oxaliplatin and Docetaxel (FLOT) in Patients With Locally Advanced, Resectable Gastric Cancer or Gastroesophageal Junction Adenocarcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Recruiting
Study Start Date
September 26, 2019 (Actual)
Primary Completion Date
March 31, 2022 (Anticipated)
Study Completion Date
June 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tianjin Medical University Cancer Institute and Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Gastric cancer is one of the most common malignant tumors of the digestive tract. Gastric cancer patients diagnosed for the first time in China have a higher proportion of advanced stages and a higher postoperative metastasis rate. Studies have shown that patients with good pathological response after preoperative neoadjuvant therapy (such as tumor regression grade, TRG0 or 1) have a better prognosis. The AIO-FLOT4 study found that preoperative perioperative FLOT chemotherapy not only prolonged the progression-free survival (PFS) time and overall survival (OS) time of patients with advanced gastric cancer, but also increased postoperative pathological remission rate. How to further improve the efficacy of the perioperative treatment plan may be beneficial to improve the long-term survival of gastric cancer patients. Several clinical studies have also confirmed that PD-1 antibody significantly prolongs the life of gastric cancer patients who have failed advanced chemotherapy in the back-line treatment. Thus the investigators plan to conduct this clinical trials to evaluate the safety and efficacy of Toripalimab (PD-1 antibody) combined with FLOT regimen in the perioperative period.The secondary end points included pathological remission rate, resection rate, D2 radical resection rate, 5-year disease-free survival (DFS) rate and 5-year OS rate.
Detailed Description
Gastric cancer is one of the most common malignant tumors of the digestive tract, accounting for the second incidence of malignant tumors, and the third mortality factor related to malignant tumors. In China, most patients with gastric cancer diagnosed for the first time are already in the advanced stage, with stage II and III patients accounting for 63%, and the postoperative recurrence rate is higher. Studies have shown that patients with good pathological response after preoperative neoadjuvant therapy (such as TRG0 or 1) have a better prognosis. In recent years, the AIO-FLOT4 study have found that perioperative chemotherapy with FLOT regimen has prolonged the PFS and OS in patients with advanced gastric cancer. It is preferred to recommend perioperative chemotherapy with FLOT regimen for patients with advanced gastric cancer in the NCCN guidelines or Chinese CSCO guidelines. How to further improve the efficacy of the perioperative treatment plan may be beneficial to improve the long-term survival of gastric cancer patients. Several clinical studies have also confirmed that PD-1 antibody significantly prolongs the life of gastric cancer patients who have failed advanced chemotherapy in the back-line treatment. In the KEYNOTE-059 study, the effectiveness of chemotherapy combined with PD-1 antibody in gastric cancer patients newly treated reached 62%. It is necessary to explore the efficacy of PD-1 antibody combined with FLOT regimen in the perioperative period. Thus the investigators plan to conduct this clinical trials to evaluate the safety and efficacy of Toripalimab (PD-1 antibody) combined with FLOT regimen in the perioperative period.The secondary end points included pathological remission rate, resection rate, D2 radical resection rate, 5-year DFS rate and 5-year OS rate.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Cancer
Keywords
Gastric Cancer, Neoadjuvant Chemotherapy, Immunotherapy, Toripalimab, Pathological Remission

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
This is an open-label, non-randomized, phase II clinical trial
Masking
None (Open Label)
Allocation
N/A
Enrollment
35 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Toripalimab combined with FLOT
Arm Type
Experimental
Arm Description
In the perioperative period, patients with resectable gastric cancer is treated with flot regimen combined with Toripalimab to observe whether the 3-year disease-free survival (DFS) rate, pathological remission rate, R0 resection rate, D2 radical resection rate, 5-year DFS rate and 5-year OS rate could be improved.
Intervention Type
Drug
Intervention Name(s)
Toripalimab
Other Intervention Name(s)
JS001
Intervention Description
240mg d1
Intervention Type
Drug
Intervention Name(s)
Docetaxel
Intervention Description
50mg/m2, d1;
Intervention Type
Drug
Intervention Name(s)
Fluorouracil
Intervention Description
2600 mg/m², d1
Intervention Type
Drug
Intervention Name(s)
Leucovorin
Intervention Description
200 mg/m², d1
Intervention Type
Drug
Intervention Name(s)
Oxaliplatin
Intervention Description
85 mg/m², d1
Primary Outcome Measure Information:
Title
3-year Disease-Free Survival Rate
Description
The primary end point of the study is the effect of perioperative time flot regimen combined with Toripalimab and D2 radical operation on the 3-year disease-free survival time of resectable gastric cancer.
Time Frame
Up to 3 years
Title
Pathological complete response rate (pCR)
Description
Proportion of patients with gastric cancer who received Toripalimab combined with FLOT regimen after 4 cycles of neoadjuvant therapy and postoperative pathological examination TRG1a
Time Frame
Up to 6 months
Secondary Outcome Measure Information:
Title
Major pathological (complete and nearly complete) response (MPR)
Description
Proportion of patients with gastric cancer who received Toripalimab combined with FLOT regimen after 4 cycles of neoadjuvant therapy and postoperative pathological examination TRG1a or 1b.
Time Frame
Up to 6 months
Title
Adverse Events
Description
For any adverse reactions, the researchers refer to the National Cancer Institute (NCI) standard of common toxicity (CTC)
Time Frame
Up to 6 months
Title
5-year Disease-Free Rate
Description
The proportion of patients with resectable gastric cancer who have no recurrence or metastasis after 5 years of perioperative treatment
Time Frame
Up to 5 years
Title
5-year Survival Rate
Description
Proportion of patients with resectable gastric cancer who survived 5 years after perioperative treatment
Time Frame
Up to 5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: locally advanced (>T1) and/or nodal positive (N+) histologically proven adenocarcinoma of the gastric or gastroesophageal junction without distant metastases (M0) no previous surgical resection no previous cytostatic chemotherapy Age > 18 years, no more than 75 years (female and male) Karnofsky Performance Status score of physical condition is 80-100 surgical resectability Exclusion of peritoneal carcinomatosis (if clinically suspected) via laparoscopy Leucocytes > 4.000/µl Platelets > 100.000/µl Serum creatinin ≤ 1.5x of normal value, or Creatinin-Clearance > 50 ml/min written informed consent. Exclusion Criteria: Distant metastasis or local invasion of adjacent organs; Recurrent or residual gastric cancer; Having or having had autoimmune disease; Previous organ transplantation or HIV patients; Allergy or contraindications to Toripalimab, 5- Fluorouracil, Leucovorin, Oxaliplatin, and Docetaxel; Malignant secondary disease; Severe non-surgical disease or acute infection; Peripheral polyneuropathy > NCI grad I; Blood system, liver and kidney function were damaged; Symptomatic brain metastasis; Obvious arrhythmia, myocardial ischemia, severe atrioventricular block, cardiac insufficiency and severe gravity valve disease; Psychotic subjects who are not easy to control; Pregnant or lactating subjects.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hongli Li, Dr
Phone
8618622221233
Email
hongli@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Jinyu Deng, Dr
Phone
8618622228656
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hongli Li, Dr
Organizational Affiliation
Tianjin Medical University Cancer Institute & Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tianjin Medical University Cancer Institute & Hospital
City
Tianjin
State/Province
Tianjin
ZIP/Postal Code
300060
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shaohua Ge, Dr
Phone
8602223340123
Ext
1051
Email
hongli@126.com

12. IPD Sharing Statement

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Toripalimab Combined With FLOT Neoadjuvant Chemotherapy in Patients With Resectable Gastric Cancer

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