Stomach Neoplasm
Conditions
Keywords
Stomach Neoplasm, Elderly Patients, Laparoscopic D1 Lymphadenectomy
Brief summary
The purpose of this study is to explore the clinical outcomes of laparoscopic D1 lymphadenectomy for elderly patients with advanced gastric adenocarcinoma（cT2-4a, N-/+, M0）
Detailed description
Gastrectomy with D2 lymphadenectomy is considered the gold standard treatment for advanced gastric cancer. However, some studies show that age or comorbidities is the relevant predictor of postoperative complications, conditioning the safety of the surgical procedure itself, thus affect the survial. Even with the advances in surgical techniques and care, age still is a significant risk for postoperative morbidity and mortality. Therefore, elderly patients with gastric cancer could receive minimally invasive surgery with reduced nodal dissection, i.e., D1 lymphadenectomy, in order to prevent postoperative complications. Laparoscopic surgery is a minimally invasive operation and is proved to be an acceptable alternative to open surgery. At present, there is no RCTs to confirm the safety and effectiveness of laparoscopic D1 lymphadenectomy for elderly patients with advanced gastric adenocarcinoma. This study is to compare the clinical outcomes of laparoscopic D1 versus D2 lymphadenectomy for elderly patients with advanced gastric adenocarcinoma（cT2-4a, N-/+, M0）to evaluate the safety of laparoscopic D1 lymphadenectomy, and to verify its results in terms of survival in elderly patients with advanced gastric adenocarcinoma.
Interventions
PROCEDURELaparoscopic D1 Lymphadenectomy
After exclusion of T4b, bulky lymph nodes, or distant metastasis case, laparoscopic D1 Lymphadenectomy will be performed in the experimental group.
PROCEDURELaparoscopic D2 Lymphadenectomy
After exclusion of T4b, bulky lymph nodes, or distant metastasis case, laparoscopic D2 Lymphadenectomy will be performed in the comparator group.
Sponsors
Fujian Medical University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
75 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Age over or equal to 75 years 2. Primary gastric adenocarcinoma (papillary, tubular, mucinous, signet ring cell, or poorly differentiated) confirmed pathologically by endoscopic biopsy, including gastric multiple primary carcinoma 3. cT2-4a(clinical stage tumor), N-/+, M0 at preoperative evaluation according to the American Joint Committee on Cancer (AJCC) Cancer Staging Manual 8th Edition 4. expected to perform distal, total or proximal gastrectomy to obtain R0 resection sugicall results. 5. Performance status of 0 or 1 on ECOG (Eastern Cooperative Oncology Group) scale 6. ASA (American Society of Anesthesiology) class I to III 7. Written informed consent
Exclusion criteria
1. Severe mental disorder 2. History of previous upper abdominal surgery (except laparoscopic cholecystectomy) 3. History of previous gastric surgery (including ESD/EMR (Endoscopic Submucosal Dissection/Endoscopic Mucosal Resection )for gastric cancer) 4. Enlarged or bulky regional lymph node （diameter over 3cm）supported by preoperative imaging 5. History of other malignant disease within the past 5 years 6. History of previous neoadjuvant chemotherapy or radiotherapy 7. History of unstable angina or myocardial infarction within the past 6 months 8. History of cerebrovascular accident within the past 6 months 9. History of continuous systematic administration of corticosteroids within 1 month 10. Requirement of simultaneous surgery for other disease 11. Emergency surgery due to complication (bleeding, obstruction or perforation) caused by gastric cancer 12. FEV1\<50% of the predicted values
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 3-year disease specific survival rate | 36 months | the rate of 3-year disease specific survival |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| 3-year disease free survival rate | 36 months | the rate of 3-year disease free survival |
| number of retrieved lymph nodes | 1 day | number of retrieved lymph nodes |
| number of positive lymph nodes | 1 day | number of positive lymph nodes |
| intraoperative blood loss | 1 day | intraoperative blood loss |
| the rate of conversion to laparotomy | 1 day | the rate of conversion to laparotomy |
| overall postoperative morbidity rate | 30 days | Refers to the incidence of early postoperative complications. The early postoperative complication are defined as the event observed within 30 days after surgery. |
| overall postoperative mortality rate | 30 days | the rate of surgical mortality |
| Time to first ambulation | 30 days | Time to first ambulation in hours is used to assess the postoperative recovery course. |
| 3-year overall survival rate | 36 months | the rate of 3-year overall survival rate |
| Time to first liquid diet | 30 days | Time to first liquid diet in days is used to assess the postoperative recovery course. |
| Time to first soft diet | 30 days | Time to first soft diet in days is used to assess the postoperative recovery course. |
| Duration of postoperative hospital stay | 30 days | Duration of postoperative hospital stay in days is used to assess the postoperative recovery course. |
| The variation of white blood cell count | Preoperative 3 days and postoperative 1, 3, and 5 days | The values of white blood cell count from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded to access the inflammatory and immune response. |
| The variation of hemoglobin | Preoperative 3 days and postoperative 1, 3, and 5 days | The values of hemoglobin in gram/liter from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded to access the inflammatory and immune response. |
| The variation of C-reactive protein | Preoperative 3 days and postoperative 1, 3, and 5 days | The values of C-reactive protein IN milligram/liter from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded to access the inflammatory and immune response. |
| The variation of prealbumin | Preoperative 3 days and postoperative 1, 3, and 5 days | The values of prealbumin in gram/liter from peripheral blood before operation and on postoperative day 1, 3, 5 are recorded to access the inflammatory and immune response. |
| operation time | 1 day | operation time |
| Time to first flatus | 30 days | Time to first flatus in days is used to assess the postoperative recovery course. |
Countries
China
Outcome results
None listed