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Clinical Trial for Laparoscopic D2 Gastrectomy (NCC181)

Primary Purpose

Gastric Cancer

Status
Completed
Phase
Phase 2
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Laparoscopic D2 distal gastrectomy
Sponsored by
National Cancer Center, Korea
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastric Cancer focused on measuring D2 lymph node dissection

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Histologically confirmed adenocarcinoma of the stomach,
  • Age between 18 and 75 years, performance status of ECOG 0-1
  • Signed informed consent
  • Location of the primary tumor in the antrum, angle and lower body
  • No evidence of distant metastasis or invasion to adjacent organs or serosal infiltration,
  • Enlarged lymph node size 2 cm or less on CT and no conglomerate nodes or regional
  • Lymph node metastasis confined to perigastric nodes (N1) as shown on by CT and EUS

Exclusion Criteria:

  • Metastatic disease, previous history of malignancy in any organ, any co-morbidity
  • Obviating major surgery, contraindication to laparoscopy such as severe cardiac disease
  • Abdominal wall hernias, diaphragmatic hernias, uncorrected coagulopathies, portal hypertension, pregnancy, previous upper abdominal surgery, complicated cases requiring emergency surgery, and an accompanying surgical condition requiring surgery at the same time

Sites / Locations

  • National Cancer Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Laparoscopic D2 gastrectomy

Arm Description

Outcomes

Primary Outcome Measures

Compliance of lymph node dissection
noncompliance : if two or more nodal station is vacant, it is a noncompliant D2 gastrectomy.

Secondary Outcome Measures

Proportion of patients with retrieved lymph nodes less than 26
operative complications
intra, and postopertive complications related to operation.
operative time
estimated blood loss
blood loss during operation.
amount of administered analgesics
time to diet
time to return of bowel movement
hospital stay
distance to resection margin and number of harvested lymph nodes

Full Information

First Posted
July 15, 2010
Last Updated
July 16, 2010
Sponsor
National Cancer Center, Korea
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1. Study Identification

Unique Protocol Identification Number
NCT01163812
Brief Title
Clinical Trial for Laparoscopic D2 Gastrectomy
Acronym
NCC181
Official Title
A Phase-II Clinical Trial of Laparoscopy-Assisted Distal Gastrectomy With D2 Lymph Node Dissection for Gastric Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
July 2010
Overall Recruitment Status
Completed
Study Start Date
April 2006 (undefined)
Primary Completion Date
October 2006 (Actual)
Study Completion Date
October 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National Cancer Center, Korea

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Objectives of this study was to determine whether laparoscopy-assisted distal gastrectomy (LADG) with complete D2 lymph node dissection for gastric cancer is a safe and effective surgical option. Methods: total 64 patients, who are diagnosed preoperatively as having T1-2, N0-1 or M0 gastric cancer, will be prospectively enrolled to undergo LADG with D2 lymph node dissection; two surgeons with experience of over 50 cases of laparoscopic gastrectomy performed the procedures. The compliance rate, defined as cases with no more than one missing lymph node station according to the Japanese Research Society of Gastric Cancer (JRSGC) lymph node grouping, for the open gastrectomy with D2 lymph node dissection was 66.0% in a pilot study and was used for calculations of sample size. Compliance rate and other surgical outcomes, including the number of retrieved lymph nodes from each lymph node station, morbidities, mortalities and conversion rate will be analyzed.
Detailed Description
Gastric cancer is the most common cancer in Korea; the overall age-standardized incidence rates of gastric cancer in Korea have been reported to be 69.6 per 100,000 among males and 26.8 per 100,000 among females in 2000. Treatment modalities for resectable gastric cancer include endoscopic mucosal resection (EMR), laparoscopy-assisted gastrectomy (LAG) and conventional open gastrectomy. Laparoscopic cancer surgery has been reported to be an acceptable alternative to open surgery in patients with colorectal cancer. However, in gastric cancer, laparoscopic surgery has not yet been validated and, thus, is performed only in a limited number of patients with early gastric cancer; this is due to the technical difficulty in systematic lymph node dissection. For the treatment of advanced gastric cancer (AGC), in countries including Korea and Japan, gastrectomy with D2 lymph node dissection has been the standard operation. With the recent progress in diagnostic techniques, accumulation of experience with laparoscopy-assisted distal gastrectomy (LADG) for early gastric cancer and the increasing interest in a better quality of life, there has been an effort to apply minimally invasive techniques to the treatment of AGC. However, there has been no clinical trial to test the oncological feasibility of LADG with D2 lymph node dissection. There is only one phase-II study that evaluated whether the morbidity associated with LADG was higher than that of open gastrectomy. Before the indications for LADG can be extended to include patients with advanced cancer, the status of surgical expertise for complete D2 lymph node dissection requires investigation using a prospective clinical study design. If this approach is shown to be feasible, a randomized prospective clinical trial, to compare survival and other surgical outcomes, would be the next step in validating this technique for this group of patients. This study is to be performed according to the Helsinki Declaration. The study was approved by the Ethics Subcommittee at the National Cancer Center for Research Involving Human Subjects (no. NCCCTS-2005181). All patients will be provided written informed consent before entering the study. Sample size The sample size was based on the alpha error at 0.05 and 90% of power and the accepted margin of the difference in the compliance rate at 10% based on a non-inferiority test. The target was chosen from the primary end point of the study. For the patients who underwent LADG with D2 lymph node dissection, the compliance rate-defined as cases in which there was no more than one missing lymph node station according to the guidelines of "The Japanese Research Society for Gastric Cancer" (JRSGC) lymph node grouping,11,12-was set up to 55%; for the patients with open distal gastrectomy with D2 lymph node dissection, it was 66%, based on a pilot study. We performed a pilot study to determine the compliance rate in 100 cases of open distal gastrectomy with D2 lymph node dissection before enrollment started. When the data was used for the formula, the total sample size required was determined to be 60 patients. When we added 10% for expected follow-up loss, the total sample size was calculated to be 66 patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Cancer
Keywords
D2 lymph node dissection

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
64 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Laparoscopic D2 gastrectomy
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic D2 distal gastrectomy
Other Intervention Name(s)
LADG
Intervention Description
Under general endotracheal anesthesia, Five or six ports are used. Lymph node dissection and ligation of vessels are carried out in the laparoscopic field. A partial omentectomy encompassing perigastric nodes is performed laparoscopically. D2 lymphadenectomy is carried out according to the guidelines of the "The Japanese Research Society for Gastric Cancer" for the corresponding location of the primary tumor. A 5- to 6-cm small incision is made transversely in RUQ of the abdomen. Through the incisional window, the stomach is removed from the abdominal cavity and resected. A Billroth-I gastroduodenostomy using an EEA stapler and GIA or a Billroth-II gastrojejunostomy with a hand-sewing technique is performed. The abdomen is then closed after hemostasis is achieved.
Primary Outcome Measure Information:
Title
Compliance of lymph node dissection
Description
noncompliance : if two or more nodal station is vacant, it is a noncompliant D2 gastrectomy.
Time Frame
immediate postoperative 1 week
Secondary Outcome Measure Information:
Title
Proportion of patients with retrieved lymph nodes less than 26
Time Frame
Postoperative 1 week
Title
operative complications
Description
intra, and postopertive complications related to operation.
Time Frame
Postoperative 1 month
Title
operative time
Time Frame
postoperative 1 day
Title
estimated blood loss
Description
blood loss during operation.
Time Frame
postoperative 1 day
Title
amount of administered analgesics
Time Frame
Postoperative 1 week
Title
time to diet
Time Frame
postoperative 1 week
Title
time to return of bowel movement
Time Frame
postoperative 1 week
Title
hospital stay
Time Frame
postoperative 1 week
Title
distance to resection margin and number of harvested lymph nodes
Time Frame
postoperative 1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically confirmed adenocarcinoma of the stomach, Age between 18 and 75 years, performance status of ECOG 0-1 Signed informed consent Location of the primary tumor in the antrum, angle and lower body No evidence of distant metastasis or invasion to adjacent organs or serosal infiltration, Enlarged lymph node size 2 cm or less on CT and no conglomerate nodes or regional Lymph node metastasis confined to perigastric nodes (N1) as shown on by CT and EUS Exclusion Criteria: Metastatic disease, previous history of malignancy in any organ, any co-morbidity Obviating major surgery, contraindication to laparoscopy such as severe cardiac disease Abdominal wall hernias, diaphragmatic hernias, uncorrected coagulopathies, portal hypertension, pregnancy, previous upper abdominal surgery, complicated cases requiring emergency surgery, and an accompanying surgical condition requiring surgery at the same time
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Young-Woo Kim, MD, PhD
Organizational Affiliation
NCC Korea
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Cancer Center
City
Goyang
State/Province
Gyeonggido
ZIP/Postal Code
411-769
Country
Korea, Republic of

12. IPD Sharing Statement

Citations:
PubMed Identifier
18340493
Citation
Ryu KW, Kim YW, Lee JH, Nam BH, Kook MC, Choi IJ, Bae JM. Surgical complications and the risk factors of laparoscopy-assisted distal gastrectomy in early gastric cancer. Ann Surg Oncol. 2008 Jun;15(6):1625-31. doi: 10.1245/s10434-008-9845-x. Epub 2008 Mar 14.
Results Reference
background
PubMed Identifier
17705092
Citation
Lee JH, Kim YW, Ryu KW, Lee JR, Kim CG, Choi IJ, Kook MC, Nam BH, Bae JM. A phase-II clinical trial of laparoscopy-assisted distal gastrectomy with D2 lymph node dissection for gastric cancer patients. Ann Surg Oncol. 2007 Nov;14(11):3148-53. doi: 10.1245/s10434-007-9446-0. Epub 2007 Aug 20.
Results Reference
result
PubMed Identifier
19430842
Citation
Lee SE, Kim YW, Lee JH, Ryu KW, Cho SJ, Lee JY, Kim CG, Choi IJ, Kook MC, Nam BH, Park SR, Kim MJ, Lee JS. Developing an institutional protocol guideline for laparoscopy-assisted distal gastrectomy. Ann Surg Oncol. 2009 Aug;16(8):2231-6. doi: 10.1245/s10434-009-0490-9. Epub 2009 May 9.
Results Reference
result

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Clinical Trial for Laparoscopic D2 Gastrectomy

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