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Robotic Versus Laparoscopic Distal Gastrectomy With D2 Lymphadenectomy for Locally Advanced Gastric Cancer

Not Applicable
Conditions
Gastric Cancer
Interventions
Procedure: Robotic distal gastrectomy with D2 nodal dissection
Procedure: Laparoscopic distal gastrectomy with D2 nodal dissection
Registration Number
NCT03273920
Lead Sponsor
Southwest Hospital, China
Brief Summary

This study is an investigator-initiated, randomized, controlled, parallel group, and non-inferiority trial comparing robot-assisted gastrectomy with D2 nodal dissection for locally advanced gastric cancer patients with laparoscopic procedure.

Detailed Description

Since the first case of laparoscopy-assisted distal gastrectomy was reported in 1994, the number of patients undergoing the laparoscopic procedure has gradually increased. The latest Japanese gastric cancer treatment guideline recommends laparoscopic gastrectomy (LG) as an optional treatment for cStage I gastric cancer (GC). Based on the experience of early GC, most experienced surgeons have applied the laparoscopic procedure in patients with locally advanced gastric cancer (AGC). According to the results of large-scaled retrospective studies and ongoing randomized controlled trials (RCTs), LG treating AGC can gain better short-term outcomes and comparable long-term oncologic results.

To minimize the limitations of laparoscopic surgery, robot systems have been introduced to treat GC providing technical advantages. Though the feasibility and safety of robotic gastrectomy (RG) have been well accepted, the benefits of RG remain controversial. A recent meta-analysis including eleven studies of 3503 patients demonstrated that RG indicated potentially favorable outcomes in terms of blood loss compared with LG. Furthermore, it has been confirmed that robotic system could provide an advantage over LG in the dissection of the N2 area lymph nodes, especially around the splenic artery area. Our previous study demonstrated that the RG had less intraoperative blood loss and more lymph nodes dissection compared with the laparoscopic procedure. However, the only prospective study reported that RG is not superior to LG in terms of perioperative surgical outcomes. Nevertheless, the following subgroup analysis found that patients with GC undergoing D2 lymph node dissection can benefit from less blood loss when a robotic surgery system is used. Take together, RG with D2 nodal dissection may be superior laparoscopic surgery in terms of blood loss and retrieved lymph nodes. However, lack of high-level evidence-based medical researches, we can't drew a conclusion that patients with AGC may benefit from RG with D2 nodal dissection.

With regard to a new surgical approach, oncologic safety has attracted more attention. Although some retrospective studies have demonstrated that RG with lymphadenectomy for GC had non-inferior oncologic outcome relative to LG, there is no prospective RCT to evaluate the long-term outcomes of RG. Therefore, the Chinese Robotic Gastrointestinal Surgery Study (CRASS) Group launched a multicenter prospective RCT to verify the short-term and long-term outcomes of RG in AGC. The primary objective of this study is to assess whether robot-assisted distal gastrectomy is comparable to laparoscopic approach in terms of long-term oncologic outcomes without compromising relapse-free survival. The secondary research objectives are to compare robotic and laparoscopic approach in terms of morbidity, mortality, quality of life, cost-effectiveness, and overall survival.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
1110
Inclusion Criteria
  1. Pathologically proven gastric adenocarcinoma.
  2. Tumor located in the lower third of the stomach, and is possible to be curatively resected by subtotal gastrectomy.
  3. Preoperative stage of cT2-4aN0-3M0 according to American Joint Committee on Cancer/Union for International Cancer Control 8th edition
  4. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  5. American Society of Anesthesiology (ASA) score of class I to III
  6. Patients who freely give informed consent to participate in the clinical study
Exclusion Criteria
  1. Previous upper abdominal surgery (except laparoscopic cholecystectomy)
  2. Previous gastric resection (gastrectomy, endoscopic mucosal resection, or endoscopic submucosal dissection)
  3. Gastric cancer-related complications (complete obstruction or perforation)
  4. Enlarged or bulky regional lymph node diameter larger than 3 cm based on preoperative imaging
  5. Previous neoadjuvant chemotherapy or radiotherapy for gastric cancer
  6. Patients diagnosed with other malignancy within 5 years
  7. Severe mental disorder
  8. Unstable angina or myocardial infarction within the past 6 months
  9. Cerebrovascular accident within the past 6 months
  10. Severe respiratory disease (FEV1< 50%)
  11. Continuous systemic steroid therapy within 1 month before the study
  12. Pregnant or breast-feeding women

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Robotic gastrectomyRobotic distal gastrectomy with D2 nodal dissectionRobotic distal gastrectomy with D2 nodal dissection
Laparoscopic gastrectomyLaparoscopic distal gastrectomy with D2 nodal dissectionLaparoscopic distal gastrectomy with D2 nodal dissection
Primary Outcome Measures
NameTimeMethod
3-year relapse-free survival3 years

Relapse-free survival is defined as days from surgery to recurrence or death from any cause, and it is censored at the latest day when the patient is alive without any evidence of recurrence.

Secondary Outcome Measures
NameTimeMethod
Mortality30 days

Postoperative mortality is defined to death that occurs within 30 days.

3-year overall survival3 years

Overall survival is defined as days from surgery to death from any cause, and it is censored at the last day when the patient was alive.

Postoperative recovery course15 days

Time to first ambulation, flatus, liquid diet, soft diet, and duration of hospital stay are used to assess the postoperative recovery course.

Morbidity30 days

Early postoperative morbidity confined to events that occur within 30 days after surgery. The complications that occur after postoperative day 30 belong to late postoperative morbidity

3-year recurrence pattern3 years

Recurrence patterns are classified into five categories at the time of first diagnosis: locoregional, hematogenous, peritoneal, distant lymph node, and mixed type.

Immune response7 days

The values of relevant immune cytokines from peripheral blood before operation and on postoperative day 1, 3, 5, 7 are recorded.

Inflammatory response7 days

The daily highest body temperature before discharge and the values of white blood cell count (10\^9/L), hemoglobin (g/L), C-reactive protein (mg/L) and prealbumin (mg/L) from peripheral blood before operation and on postoperative day 1, 3, 5, 7 are recorded.

Trial Locations

Locations (14)

The Second Xiangya Hospital of Central South University

🇨🇳

Changsha, Hunan, China

Wuhan Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

🇨🇳

Wuhan, Hubei, China

Jilin Cancer Hospital

🇨🇳

Changchun, Jilin, China

Xijing Hospital of Digestive Dieases

🇨🇳

Xi'an, Shanxi, China

West China Hospital, Sichuan University

🇨🇳

Chengdu, Sichuan, China

Chinese PLA general hospital

🇨🇳

Beijing, Beijing, China

Department of General Surgery and Center of Microinvasive Gastrointestinal Surgery, Southwest Hospital

🇨🇳

Chongqing, Chongqing, China

Peking University Cancer Hospital

🇨🇳

Beijing, Beijing, China

Fujian Medical University Union Hospital

🇨🇳

Fuzhou, Fujian, China

Lanzhou PLA General Hospital

🇨🇳

Lanzhou, Gansu, China

Sun Yat-sen University Cancer Center

🇨🇳

Guangzhou, Guangdong, China

Nanjing General Hospital

🇨🇳

Nanjing, Jiangsu, China

The First Affiliated Hospital of Nanchang University

🇨🇳

Nanchang, Jiangxi, China

The Affiliated Hospital of Qingdao University

🇨🇳

Qingdao, Shandong, China

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