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Completed

NCT Number: NCT04354662

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

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.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Tianjin Medical University Cancer Institute & Hospital

Tianjin, Tianjin Municipality, 300060, China

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Toripalimab

Drug

240mg d1

Other names: JS001

docetaxel

Drug

50mg/m2, d1;

Fluorouracil

Drug

2600 mg/m², d1

Leucovorin

Drug

200 mg/m², d1

Oxaliplatin

Drug

85 mg/m², d1

Primary outcomes

  1. Pathological complete response rate (pCR)

    Time frame: Up to 6 months

    Proportion of patients with gastric cancer who received Toripalimab combined with FLOT regimen after 4 cycles of neoadjuvant therapy and postoperative pathological examination TRG 0

  2. 3-year Disease-Free Survival Rate

    Time frame: Up to 3 years

    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.

Secondary outcomes

  1. Major pathological (complete and nearly complete) response (MPR)

    Time frame: Up to 6 months

    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.

  2. Adverse Events

    Time frame: Up to 6 months

    For any adverse reactions, the researchers refer to the National Cancer Institute (NCI) standard of common toxicity (CTC)

  3. 5-year Disease-Free Rate

    Time frame: Up to 5 years

    The proportion of patients with resectable gastric cancer who have no recurrence or metastasis after 5 years of perioperative treatment

  4. 5-year Survival Rate

    Time frame: Up to 5 years

    Proportion of patients with resectable gastric cancer who survived 5 years after perioperative treatment

Sponsors and collaborators

Lead sponsor

Tianjin Medical University Cancer Institute and Hospital

Other

Registry information

Official study 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

Important dates

Study start
2020
Primary completion
2022
Study completion
2026
First posted
Apr 21, 2020
Registry last updated
Aug 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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