Gastric Cancer Clinical Trial
Official title:
Prospective Multicenter Randomized Controlled Clinical Trial for Comparison Between Laparoscopic and Open Subtotal Gastrectomy With D2 Lymph Node Dissection for Locally Advanced Gastric Cancer
- It was confirmed that the laparoscopic surgery decreases the postoperative pain and
reduces the recovery periods in the various surgical fields such as cholecystectomy and
colectomy etc. Also, there are clinical evidences that the laparoscopic surgery is
applicable to malignant tumor according to the development of surgical techniques and
medical instruments.
- In case of early stage of gastric cancer, as the diverse clinical evidences, the
gastrectomy has been commonly applied, however, the opening surgery is still applied for
advanced gastric cancer due to lack of clinical evidence.
- In Korea, approximately 38% of patients who undergo surgery for gastric cancer are
diagnosed by T2-T3 (AJCC 6th edition) (www.i-kgca.or.kr, National gastric cancer
registration business in 2009). There are various clinical evidences to apply
laparoscopic surgery to the patients, however, most of them are retrospective or cohort
study results.
- For the clinical application of surgical treatment regarding locally advanced gastric
cancer using laparoscopic surgical technique, it requires the confirmation of definite
execution for laparoscopic gastrectomy and D2 lymph node dissection and the safety of
surgery and oncological usefulness should be verified.
- In order for this, it is only possible to confirm through the comparison of short-term
surgical results (complications, mortalities, operative time and duration of
hospitalization etc) and long-term results (survival rates and recurrence rates etc)
between laparoscopic surgery and opening surgery based on the multicenter large-sized
randomized prospective study with current standard treatment.
Participating Surgeons
- Prior to this clinical trial, only the surgeons who are considered to have the
standardization by participating the assignment entitled with "KLASS-02-QC:
Standardization of D2 Lymphadenectomy and Surgical Quality Control for KLASS-02
Trial"(ClinicalTrials.gov No: NCT01283893).
Patients Registration
- It is required to ensure that the patients meet the inclusion criteria for this clinical
trial, are free from any items of exclusion criteria, are explained about the
participation in the clinical trial along with the informed consent forms.
- After rechecking the patients with the registration check list by accessing the
web-based randomized program provided from Ajou University clinical trial center.
Randomization
- The registration randomization should be done with 1:1 ratio for each researcher.
- Baseline number (BN) should be provided to the subjects in the order of acquisition of
informed consent form. Based on the subjects who are selected as the appropriate
subjects in the end, the allocation number (AN) shall be provided in the order of
randomized allocation table.
Procedure
- Operations are performed according to the allocated group.
Adjuvant Treatment
- If it is under Stage II and Stage III in the final postoperative pathology, the adjuvant
chemotherapy based on 5-FU.
Evaluation of efficacy and safety
- 3-year Relapse free survival rate and overall survival rate of the patients who undergo
laparoscopic and open subtotal gastrectomy and D2 lymph node dissection.
- Analysis of recovery after laparoscopic and open subtotal gastrectomy and D2 lymph node
dissection.
- Postoperative complications of the patients who undergo laparoscopic and open subtotal
gastrectomy and D2 lymph node dissection within postoperative 3 weeks and later.
- The quality of life at preoperative, postoperative 25 days and 1 years using recovery
index such as recovery of postoperative intestinal hypermotility, meals and duration of
hospitalization, EORTC-C30 and STO22 questionnaire between the patients who underwent
laparoscopic and open subtotal gastrectomy and D2 lymph node dissection.
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