Clinical trial Recruiting at 1 site Observational Ages 18 and up

Evaluating outcomes in gastric cancer patients before and after a Tumor Board implementation

Official title: Gastric Cancer' Textbook Oncological Outcome and Tumor Board Performance - The Experience of a High-volume Italian University Hospital

Run by Fondazione Policlinico Universitario Agostino Gemelli IRCCS · NCT06923449 · Data updated 2026-11-12

This study is trying to see if having a team of experts work together improves the surgery and treatment results for people with gastric cancer.

More Stomach Neoplasm trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment250 (estimated)
SponsorFondazione Policlinico Universitario Agostino Gemelli IRCCS
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Rome, IT)
StatusRecruiting
StartedMay 16, 2024
Main results expectedApril 30, 2025
Study endsJune 30, 2025
Registry record updatedApril 11, 2025
Trial IDNCT06923449 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults aged 18 and older with a confirmed diagnosis of gastric adenocarcinoma who are surgical candidates.

Probably not a fit

Patients with non-adenocarcinoma histologies, those requiring emergency treatment, or those under 18 years old may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to compare surgical and oncologic outcomes in gastric cancer patients before and after the establishment of a Multidisciplinary Tumor Board at Fondazione Policlinico Gemelli. It will assess the Textbook Outcome (TO) and Textbook Oncological Outcome (TOO) of patients undergoing surgical treatment with curative intent. The study will analyze data from 2018 to the present to evaluate the impact of the Tumor Board on patient outcomes, including treatment allocation and adherence to guidelines. The hypothesis is that the implementation of the Tumor Board will lead to improved outcomes for gastric cancer patients.

Why it matters

Potential benefit: If successful, this study could enhance the quality of care and outcomes for patients with gastric cancer.

How similar studies have gone: Previous studies have shown that structured multidisciplinary approaches can improve surgical outcomes in cancer care, suggesting potential success for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* pathology-confirmed diagnosis of gastric adenocarcinoma
* age 18 years or older
* surgical candidates with curative intent

Exclusion Criteria:

* Endoscopic Mucosal Resection (EMR) or Endoscopic Submucosal Dissection (ESD)
* previous EMR or ESD (salvage surgery)
* histologies other than adenocarcinoma (no squamous cell carcinomas, GISTs, sarcomas, lymphomas, etc)
* unsufficient staging (unclear clinical stage at diagnosis)
* emergency presentation (obstrucetd, significantly bleeding, perforated gastric cancer)
* synchronous tumors affecting survival
* pregnant patients
* age \<18years

Where it's running

  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS
    Rome, It, Italy
    Recruiting

Study contacts

  • Principal investigator: Alberto Biondi, Prof. — Fondazione Policlinico Agostino Gemelli IRCCS
  • Study coordinator: Laura Antolino, MD, PhD
  • Email: laura.antolino@gmail.com
  • Phone: +393470409876

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.