Trans-Pacific Multicenter Collaborative Study of Minimally Invasive Proximal Versus Total Gastrectomy for Proximal Gastric and Gastroesophageal Junction Cancers
Launched by M.D. ANDERSON CANCER CENTER · Jan 11, 2022
Trial Information
Current as of July 23, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying two surgical methods for treating certain types of stomach cancer: minimally invasive proximal gastrectomy (MIPG) and minimally invasive total gastrectomy (MITG). The goal is to compare how these two procedures affect patients' symptoms after surgery. Researchers want to find out which method might lead to better outcomes for patients diagnosed with non-metastatic gastric cancer or gastroesophageal junction (GEJ) adenocarcinoma who are planning to have surgery to try to cure their cancer.
To participate in the trial, patients need to be at least 18 years old and able to read and speak English, Spanish, Korean, or Japanese, depending on where they are enrolled. They must have a confirmed diagnosis of stomach cancer and be scheduled for one of the surgical procedures. Participants can expect to be monitored closely during and after their surgery to assess their symptoms and recovery. It’s important to note that some patients, such as those with certain health issues or who are pregnant, may not be eligible to join the study.
Gender
ALL
Eligibility criteria
- Inclusion:
- • 1. Able to speak and read English, Spanish, Japanese or Korean
- • 2. Participants with a biopsy-confirmed diagnosis of non-metastatic gastric or GEJ adenocarcinoma, who are scheduled to undergo MIPG or MITG for curative-intention
- • 3. Age ≥ 18
- Exclusion:
- • 1. Participants with known malabsorption syndromes or a lack of physical integrity of the upper gastrointestinal tract
- • 2. Participants with known narcotic dependence, with average daily dose \> 5 mg oral morphine equivalent
- • 3. Participants deemed unable to comply with study and/or follow-up procedures, at investigators' discretion
- • 4. Participants who are pregnant (since are excluded from receiving standard-of-care MIPG or MITG)
About M.D. Anderson Cancer Center
The University of Texas MD Anderson Cancer Center is a leading institution dedicated to cancer care, research, education, and prevention. As one of the world’s most respected cancer centers, MD Anderson focuses on innovative treatment approaches and groundbreaking clinical trials aimed at improving patient outcomes. With a multidisciplinary team of experts and state-of-the-art facilities, the center is committed to advancing cancer research and providing comprehensive, personalized care to patients. MD Anderson's clinical trials play a pivotal role in translating scientific discoveries into effective therapies, positioning the center at the forefront of cancer treatment and research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
New York, New York, United States
Houston, Texas, United States
Rochester, Minnesota, United States
New York, New York, United States
Tokyo, , Japan
Soeul, , Korea, Democratic People's Republic Of
Soeul, , Korea, Republic Of
Patients applied
Trial Officials
Naruhiko Ikoma, MD
Principal Investigator
M.D. Anderson Cancer Center
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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