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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03366961
Other study ID # ConGC-II
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date December 1, 2017
Est. completion date December 31, 2022

Study information

Verified date September 2019
Source Seoul St. Mary's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to identify the safety and the survival benefit of the conversion surgery in stage IV or unresectable gastric cancer. The study designed single-arm phase II trial. All the patients would undergo curative-intent radical gastrectomy after palliative chemotherapy if the tumor responded to the chemotherapy. Primary endpoint was three-year overall survival. Secondary endpoints included short-term postoperative outcomes within 30 days, three-year relapse free survival, and success rate of conversion surgery (rate of R0 resection).


Description:

The survival rate of patients with stage IV gastric cancer (GC) is very low. Recently, several retrospective studies about conversion surgery have been introduced. The results of the studies showed around 30~40% of three-year survival rate in conversion surgery group. Eight institutions in Catholic University of Korea analyzed 419 stage IV GC patients, and they had divided into four groups: chemotherapy only, chemotherapy followed by gastrectomy, gastrectomy followed by chemotherapy, and best supportive care group. The group of gastrectomy followed by chemotherapy, which is similar with conversion surgery, showed 40% of three-year survival rate. However, the study included only small number of patients who were in conversion surgery group, and had several biases. Thus, we planned multi-national, multi-center phase II trial for conversion surgery in stage IV or unresectable GC.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 31, 2022
Est. primary completion date December 31, 2019
Accepts healthy volunteers No
Gender All
Age group 19 Years to 80 Years
Eligibility Inclusion Criteria:

- Gastric adenocarcinoma

- Stage IV or unresectable gastric cancer was diagnosed by pre-operative evaluation including endoscopy, endoscopic ultrasound, Computed tomography (CT), Positron emission tomography-computed tomography (PET CT), or staging laparoscopy

- Partial or complete response to chemotherapy

- Eastern Cooperative Oncology Group (ECOG) score <3

- Who agreed to enroll the study

Exclusion Criteria:

- Synchronous or metachronous malignancy

- remnant gastric cancer

- BMI less than 18.5

- Pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Conversion surgery
Palliative chemotherapy followed by radical gastrectomy

Locations

Country Name City State
Korea, Republic of Seoul St. Mary's Hospital Seoul

Sponsors (3)

Lead Sponsor Collaborator
Cho Hyun Park Peking University, The Catholic University of Korea

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary 3-year overall survival 3-year overall survival after conversion surgery 3 years after the surgery
Secondary Complication Short-term complication rate after conversion surgery 30 days after the surgery
Secondary 3-year disease free survival 3-year disease free survival after conversion surgery 3 years after the surgery
Secondary Success rate of conversion surgery Rate of R0 resection 30 days after the surgery
Secondary Response rate of chemotherapy Response rate of chemotherapy Operation day