Short-term Outcomes of Laparoscopic Versus Open Gastrectomy With Lymph Node Dissection for Early Gastric Cancer :a Randomized Controlled Study

Aim of the work

a prospective randomized controlled trial comparing laparoscopic and open gastrectomy with D2 lymph node dissection for EGC to evaluate technical safety and oncologic feasibility.

The postoperative morbidity and mortality rates will be based on the modified intention-to-treat analysis.

The aim of this study is to compare the operative and short-term oncologic outcomes of laparoscopic versus open resections.

Patients and methods

The study design: : prospective randomized comparative clinical trial study analyzing outcomes of gastrectomy for early gastric cancer using laporoscopy versus open approach. This will be a prospective comparative study at Sohag University Hospital, Egypt and National Cancer Institute(NCI), Cairo university ,Egypt.

Patients were divided randomizly into two groups; the first group included patients who will have laparoscopic gastrectomy (Lap group), and the second group included patients will receive open gastrectomy (Open group).

Study population

The study included patients complaining of gastric cancer stage (T1-T2N0M0).The study will start from december 2022 .

Inclusion criteria: Inclusion criteria were as follows: histologically confirmed adenocarcinoma of the stomach; pathologically confirmed stage T1-T2; no evidence of distant metastasis by means of abdominal computed tomography(CECT) and CT chest ; D2 lymphadenectomy with curative R0

according to pathological diagnosis after the operation . patients with N1 confirmed pathologically after operation also will be included in the study.

The exclusion criteria:

1. pregnancy
2. an American Society of Anesthesiologists (ASA) score > 3,
3. severe mental disorders
4. prior upper abdominal surgery except laparoscopic cholecystectomy,
5. presence of other malignancies
6. a history of chemotherapy or radiation therapy.
7. unstable angina or myocardial infarction within the past 6 months, severe respiratory disease (forced expiratory volume in 1 s, FEV1 < 50%)
8. abdominal wall hernia
9. diaphragmatic hernia
10. coagulation disorder
11. portal hypertension
12. Advanced gastric cancer (stage;T3,T4,N1 to 3 ,M1) based on preoperative diagnosis.

Approvals and consents

This study will be done after obtaining approval from the research ethics committee of the Sohag faculty of medicine. A written Informed consent will be obtained from all participants before being enrolled in the study and before performing the procedure after receiving an explanation of the study protocol, including both types of operation and possible complications. The study will be registered at www.clinicaltrials.gov.

Data collection:

Registered data will be collected from the hospital databases, clinical data.

Randomization

Randomization was performed by closed envelopes and was balanced and stratified for proposed type of resection.