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Extensive Intraoperative Peritoneal Lavage After Curative Gastrectomy for Locally Advanced Gastric Cancer (SEIPLUS)

A Prospective, Multicentral, Open-label, Randomized, Controlled Clinical Trial to Investigation the Value of Extensive Intraoperative Peritoneal Lavage After Curative Gastrectomy for Locally Advanced Gastric Cancer

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02745509
Acronym
SEIPLUS
Enrollment
508
Registered
2016-04-20
Start date
2016-03-31
Completion date
2017-11-30
Last updated
2019-02-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastric Cancer

Keywords

Extensive Intraoperative Peritoneal Lavage, EIPL, Gastric Cancer

Brief summary

The investigators study aims to explore the potential function of extensive intraoperative peritoneal lavage in improving the overall survival and progression-free survival for locally advanced gastric cancer after curative resection. Hypothesis: Overall survival and progression-free survival of locally advanced gastric cancer are improved by extensive intraoperative peritoneal lavage.

Detailed description

Gastric cancer has been one of the most frequently common cancers and remains the third leading cause of death among malignant tumors all over the world. Surgery has always been considered as the most effective treatment. While significant surgical technique and perioperative management have dramatically improved the survival of patients with advanced gastric cancer, patients with T4 stage or serosal-positive gastric cancer often suffer from recurrence as peritoneal dissemination, and the prognosis of those patients is extremely poor. Despite curatively resected, Peritoneal metastasis is completed by the implantation of peritoneal free cancer cells exfoliated from serosa-invasive tumors. Therefore, things need to be done to eliminate the free exfoliated cancer cells on the peritoneal lining in order to reduce the risk of peritoneal recurrence. A multi-institutional prospective, randomized trial has been launched by Kuramoto recently. The trail was intended to demonstrate the superiority in overall survival of addition of Extensive Intraoperative peritoneal Lavage (EIPL) to standard treatment in patients with≥T3 carcinoma of stomach. Based on the'limiting dilution theory', after total or distal gastrectomy with D2 lymphadenectomy, the peritoneal cavity is extensively rinsed 10 times with 1 L physiological saline at a time, followed by complete aspiration of the fluid. In total, 10 L saline is to be used. In this study, the EIPL-IPC group had a significantly lower incidence of peritoneal recurrence. Furthermore, the 5-year overall survival rate of the patients in the EIPL-IPC group (43.8%) was significantly better than that of the intraperitoneal chemotherapy (IPC) group (4.6%) and the surgery-alone group (0%). All in all, EIPL is easy to carry out, safe and inexpensive. Therefore, gastrectomy with EIPL will be a new standard treatment of gastric cancer. To ensure the quality of the study, two interim analyses will be planned at the half and the completion of the study respectively. The Data and Safety Monitoring Committee will independently review the interim analysis and stop the study ahead of schedule if necessary. Furthermore, to improve the study progress and quality, the in-house interim monitoring will be performed.

Interventions

OTHERExtensive Intraoperative Peritoneal Lavage

Extensive Intraoperative Peritoneal Lavage

Sponsors

Anhui Provincial Hospital
CollaboratorOTHER_GOV
The First Affiliated Hospital of Anhui Medical University
CollaboratorOTHER
Anqing Municipal Hospital
CollaboratorOTHER
Yuebei People's Hospital
CollaboratorOTHER
The First Affiliated Hospital of Guangdong Pharmaceutical University
CollaboratorOTHER
Guangdong Provincial Hospital of Traditional Chinese Medicine
CollaboratorOTHER
Jiangsu Cancer Institute & Hospital
CollaboratorOTHER
Jiangxi Provincial Cancer Hospital
CollaboratorOTHER
Tianjin Medical University Cancer Institute and Hospital
CollaboratorOTHER
First Affiliated Hospital of Wannan Medical College
CollaboratorOTHER
Lishui hospital of Zhejiang University
CollaboratorUNKNOWN
Second Affiliated Hospital, School of Medicine, Zhejiang University
CollaboratorOTHER
Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Lower age limit of research subjects 18 years old and upper age limit of 80 years old. 2. ECOG score standard (ECOG)performance status of 0 or 1 and expected to survive more than 6 months. 3. Without any other malignancies. 4. Written informed consent from the patient. 5. Histologically proven primary gastric adenocarcinoma. 6. Patients planned for open gastrectomy. 7. Patients who have T3 (subserosal) or T4 (serosal) disease based on Ultrasound gastroscopy and intra-operative inspection with any N staging and M0 gastric cancer. 8. No preoperative neoadjuvant chemotherapy. 9. Length of esophageal invasion≤3cm and no need of thoracotomy for resection. 10. Intraoperative inclusion criteria: 1. Clinically T3, T4a or T4b. 2. Clinically H0 and M0. No peritoneal dissemination or Distant metastases. 3. Possible for R0 surgery.

Exclusion criteria

1. Female in pregnancy or lactation. 2. Supraclavicular lymph nodes metastases,pelvis or ovarian implantation,peritoneal dissemination,liver,lung and bone metastases. 3. Massive ascites or cachexia. 4. Patients participating in any other clinical trails currently,or participated in other trails within 1 months. 5. Without a history of stomach or esophageal cancers, including stromal tumor,sarcoma,lymphoma and carcinoid. 6. Suffering from other serious diseases, including cardiovascular, respiratory, kidney, or liver disease, complicated by poorly controlled hypertension, diabetes, mental disorders or diseases. 7. Patients with poor compliance or considered to be poor compliance.

Design outcomes

Primary

MeasureTime frameDescription
Overall survival3-yearThe survival rate between the surgery to the 3rd year due to all-cause death or last follow-up.

Secondary

MeasureTime frameDescription
Disease-free survival3-yearThe progression-free or all-cause death rate between the surgery and the 3rd year.
Peritoneal recurrence3-yearThe Peritoneal recurrence rate between the surgery and the 3rd year
Postoperative complicationsan average of 10 dayscomplications such bleeding, infection, obstruction and leakage
Post-operative quality of lifean average of 10 daysThe postoperative quality of life will be assessed by factors such as Swallowing,Pain and discomfort,Dietary restrictions, Upper gastrointestinal symptoms, mental status and others.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026