Gastric Cancer Clinical Trial
Official title:
Multicenter Randomized Controlled Trial for Application of Laparoscopic Total Gastrectomy With Lymph Node Dissection for Gastric Cancer (KLASS-06)
Although Laparoscopic gastrectomy for both early and locally advanced gastric cancer has
gained popularity, the use of laparoscopic total gastrectomy for proximal advanced gastric
cancer is still limited to some experienced surgeons, because of its technical difficulties
in D2 lymph node dissection and anastomoses.
Some retrospective and cohort studies regarding laparoscopic total gastrectomy with lymph
node dissection suggested the likelihood of application of laparoscopic surgery for proximal
gastric cancer. However, there has been no randomized clinical trial comparing results of
laparoscopic total gastrectomy with D2 lymph node dissection with open conventional surgery.
Therefore, we aimed to verify the efficacy of laparoscopic total gastrectomy with D2(D2-10)
lymph node dissection, technical and oncologic safety compared with open surgery via
multicenter randomized clinical trial.
Status | Recruiting |
Enrollment | 772 |
Est. completion date | December 31, 2027 |
Est. primary completion date | December 31, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Patients who are over 20 and below 80 years old - Patients who have performance status of ECOG 0 or 1 - Patients with American Society of Anesthesiology score of class I to III - Patients who are diagnosed with gastric adenocarcinoma not involving Z-line by endoscopy with biopsy - Patients with tumors which can be curatively resected by total gastrectomy with lymph node dissection based on preoperative study - Patients who have primary gastric carcinoma invaded into over muscle propria, and not into adjacent organ in preoperative studies (cT2 ~ cT4a) - Patients who have no metastasis to lymph nodes or limited metastasis to perigastric lymph node metastasis in preoperative studies (cN0 ~ cN2) - Patients who agree with participating in the clinical study with informed consents - Patients who can be followed for at least 3 years after study enrollment Exclusion Criteria: - Patients who have possibility of distant metastasis in preoperative studies - Patients who have history of gastric resection with any cause - Patients who have complications (bleeding or obstruction) of gastric cancer - Patients who are treated by chemo(radio)therapy or endoscopic submucosal dissection for gastric cancer - Patients who are diagnosed and treated with other malignancies within 5 years - Vulnerable patients - Patients who participating or participated in other clinical trial within 6 months |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Department of Surgery, Yonsei University College of Medicine, Seoul, Korea | Seoul |
Lead Sponsor | Collaborator |
---|---|
Yonsei University |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 3 year relapse-free survival | Non-inferiority of 3 year relapse-free survival rate after laparoscopic radical total gastrectomy and lymphadenectomy for locally advanced gastric cancer comparing with open conventional surgery. The "event" of relapse-free survival is defined as "recurrence" after 4 weeks of operation. The "censoring" is defined as non-traceable patient who cannot be confirmed with recurrence or patient who are alive without recurrence until follow-up. The "relapse-free survival time" is defined as the time from surgery to "event" or "censoring". |
3 years after surgery | |
Secondary | 3 year overall survival rate | 3 years after surgery | ||
Secondary | 5 year relapse-free and overall survival | 5 years after surgery | ||
Secondary | Morbidity (early period) | from Operation day until POD 21 | ||
Secondary | Morbidity (late period) | from POD (Post-Operative Day) 22 until 5 years after surgery | ||
Secondary | Mortality | death with any cause | at POD 30 | |
Secondary | Mortality | death with any cause | at POD 90 | |
Secondary | Quality of life(EORTC QLQ-C30) | Quality of life measured by EORTC QLQ-C30(Version 3) The questionnaire was designed to measure cancer patients' physical, psychological and social functions. The questionnaire is composed of 5 multiitem scales (physical, role, social, emotional and cognitive functioning) and 9 single items (pain, fatigue, financial impact, appetite loss, nausea/vomiting, diarrhea, constipation, sleep disturbance and quality of life). | at POD 21 | |
Secondary | Quality of life(EORTC QLC STO22) | Quality of life measured by EORTC QLC STO22. The EORTC QLQ-STO 22 module contains 22 items in a similar layout and response format to the EORTC QLQ-C30. The hypothesised scale structure of the module consists of five scales (dysphagia, eating restrictions, pain, reflux and anxiety) and three single items (dry mouth, body image and hair loss). | at POD 21 | |
Secondary | Quality of life(EORTC QLQ-C30) | Quality of life measured by EORTC QLQ-C30(Version 3) | 3 months after surgery | |
Secondary | Quality of life(EORTC QLC STO22) | Quality of life measured by EORTC QLC STO22. The EORTC QLQ-STO 22 module contains 22 items in a similar layout and response format to the EORTC QLQ-C30. The hypothesised scale structure of the module consists of five scales (dysphagia, eating restrictions, pain, reflux and anxiety) and three single items (dry mouth, body image and hair loss). | 3 months after surgery | |
Secondary | Quality of life(EORTC QLQ-C30) | Quality of life measured by EORTC QLQ-C30(Version 3) | 12 months after surgery | |
Secondary | Quality of life(EORTC QLC STO22) | Quality of life measured by EORTC QLC STO22. The EORTC QLQ-STO 22 module contains 22 items in a similar layout and response format to the EORTC QLQ-C30. The hypothesised scale structure of the module consists of five scales (dysphagia, eating restrictions, pain, reflux and anxiety) and three single items (dry mouth, body image and hair loss). | 12 months after surgery |
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