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NCT07241715Active, not recruitingPhase 2/3

Conversion Surgery for Gastric Cancer With Peritoneal Metastases (CONVERGENCE)

Source: ClinicalTrials.gov · Last updated 14 May 2026

Brief summary (registry, in English)

The goal of this clinical trial is to evaluate the impact of conversion surgery on overall survival (OS) in patients with gastric cancer peritoneal metastases (GCPM) who show a good response to preoperative systemic therapy (including first-line chemotherapy with or without targeted therapy and/or immunotherapy) with or without peritoneal-directed chemotherapy.\]. The main question it aims to answer is: (i) Will Conversion surgery be associated with improved overall survival (OS) in patients with GCPM who respond well to preoperative systemic therapy, compared to patients who do not undergo surgery? (ii) Will Quality of life be comparable or improved in patients who undergo conversion surgery compared to patients receiving palliative chemotherapy as measured by the QLQ-C30 questionnaire? If there is a comparison group: Researchers will compare Arm 1 (Conversion surgery with systemic therapy (including 1L chemotherapy +/- targeted therapy +/- immunotherapy) +/- peritoneal directed chemotherapy) to Arm 2 (systemic therapy alone (including 1L chemotherapy +/- targeted therapy +/- immunotherapy) +/- peritoneal directed chemotherapy) to see if the conversion surgery will be associated with improved overall survival (OS) in Arm 1. Participants will be randomized to either Arm 1 or Arm 2. * For Arm 1, participants will go for conversion surgery then continue systemic therapy. * For Arm 2, participants will continue systemic therapy. Radiological assessment will be performed every 6 months or upon progression of disease, whichever comes earlier.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
300 (estimated)
First submitted
7 Oct 2024
Start date
21 Feb 2026
Primary completion date
Jan 2034
Lead sponsor
National University Hospital, Singapore
NCT number
NCT07241715

What you commit to

  • Study type: Interventional · Phase 2/3
  • Planned participants: 300
  • From 21 Feb 2026 to the primary completion date, Jan 2034
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior surgical treatment for GC involving resection

Other

  • Pregnant and lactating females
  • Clinical or radiological progression during 1st line systemic treatment

Who the study is looking for

  • GCPM detected on surgical exploration and demonstrated by histology or cytology
  • Primary GC not resected
  • Age \> 21 (or \> 18 as allowed by individual institution review boards)

Age in the registry: 21 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
National University Hospital
Coordinator of this site? Confirm its status
SingaporeSingaporeUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.