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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03646591
Other study ID # Dragon III- Pilot study
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 15, 2017
Est. completion date August 20, 2018

Study information

Verified date November 2020
Source Ruijin Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Neoadjuvant chemotherapy for advanced-stage gastric cancer is justified by various studies, however, there was not any large scale randomized controlled trial (RCT) to support it until German oncologist introduced a novel regimen(FLOT regimen) in 2017. Investigator assessed the FLOT regimen for safety and feasibility in Chinese gastric cancer patients.


Description:

Neoadjuvant chemotherapy for advanced-stage gastric cancer is justified by various studies, however, there was not any large scale RCT to support it until German oncologist introduced a novel regimen(FLOT regimen) in 2017. FLOT regimen was prescribed for German patients and various questions are raised by experts from Eastern countries. As the FLOT regimen was officially included in NCCN 2018 guidelines, the investigator used standard protocol of FLOT regimen on Chinese gastric cancer patients. Safety and feasibility were assessed carefully to provide basic data for further large scale studies in China.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date August 20, 2018
Est. primary completion date August 20, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Sex: all - Histology confirmed adenocarcinoma of the stomach or esophagogastric junction. - Clinical stage: Clinical Tumor-Node-Metastasis (cTNM): stage III,IVa - Performance status: Eastern Cooperative Oncology Group ECOG 0- 2 - Adequate renal, hepatic, hematologic, and pulmonary function. - Written informed consent Exclusion Criteria: - Uncontrolled cardiac disease, or other clinically significant uncontrolled comorbidities - Distant metastases - Prior chemo or radiotherapy - Inclusion in another clinical trial - Known contraindications or hypersensitivity for planned chemotherapy

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Chemotherapy
Patients will receive four cycles of the standard dose of FLOT chemotherapy prior to curative gastrectomy. And four cycles of the FLOT chemotherapy is recommended after surgery. Preventive antiemetic and dexamethasone are allowed before chemotherapy, growth factor, or other supportive medicines are allowed for treatment only. Surgical intervention is allowed for acute bleeding or other surgical emergencies.

Locations

Country Name City State
China Ruijin Hospital Shanghai Jiaotong University School of Medicine Shanghai Shanhgai

Sponsors (1)

Lead Sponsor Collaborator
Ruijin Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Completion rate of preoperative FLOT regimen How many patients completed the plan preoperative chemotherapy regimen upto 3 months
Secondary Adverse events Chemotherapy related adverse events according to the CTCAE version 3.0 Upto three months
Secondary Pathological response rate According to tumor regression grading(TRG) Upto three months
Secondary Postoperative morbidity Postoperative complications Upto one month after hospital discharge
Secondary Postoperative mortality Death due to surgical complication Upto one month after hospital discharge
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