Actively Recruiting

Age: 18Years - 85Years
All Genders
NCT04842916

InteGRAtive Analysis of TuMor, Microenvironment, ImmunitY and Patient Expectation for Personalized Response Prediction in Gastric Cancer

Led by Istituto Romagnolo per lo Studio dei Tumori Dino Amadori IRST S.r.l. IRCCS · Updated on 2024-11-21

250

Participants Needed

5

Research Sites

347 weeks

Total Duration

On this page

Sponsors

I

Istituto Romagnolo per lo Studio dei Tumori Dino Amadori IRST S.r.l. IRCCS

Lead Sponsor

E

ERA PERMED

Collaborating Sponsor

AI-Summary

What this Trial Is About

Multicentric, exploratory, non-pharmacologic, retrospective/prospective, translational study aiming to identify the molecular, cellular and psychological-sociological variables predictive of response to chemotherapy in gastric cancer patients.

CONDITIONS

Official Title

InteGRAtive Analysis of TuMor, Microenvironment, ImmunitY and Patient Expectation for Personalized Response Prediction in Gastric Cancer

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with diagnosis of histologically confirmed, potentially resectable adenocarcinoma of the stomach or gastric-esophageal junction treated with standard chemotherapy regimens (5-Fluoro-Uracil or Capecitabine + Oxaliplatin +/- Docetaxel)
  • Participants willing and able to give informed consent or with substitutive consent by the investigator for unreachable patients
  • Male or female aged over 18 years
  • Availability of tissue samples and clinical-pathological data for retrospective cohort
Not Eligible

You will not qualify if you...

  • Age under 18 years
  • Early gastric cancer and T2 stage if no lymph node involvement
  • Linitis plastica
  • Positive peritoneal cytology or peritoneal involvement
  • Distant metastases
  • Patient refusal to participate
  • Patient refusal to allow use of their samples for research
  • Withdrawal from treatment due to co-morbidities or non-compliance
  • Underlying conditions making biological sampling unsafe or unusable
  • Mental illness impairing ability to provide accurate information or follow recommendations

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 5 locations

1

Centre Hospitalier Regional et Universitaire (CHRU)

Brest, France, 29200

Not Yet Recruiting

2

INSERM, Faculty of Medicine (UMR1078)

Brest, France, 29200

Active, Not Recruiting

3

1st Department of Propaedeutic Surgery, National & Kapodistrian University of Athens (NKUA)

Athens, Greece, 11527

Not Yet Recruiting

4

IRST IRCCS UO Oncologia

Meldola, Italy, 47014

Actively Recruiting

5

AUSL Romagna, UO Oncologia

Ravenna, Italy, 48121

Active, Not Recruiting

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Research Team

C

Chiara Molinari

CONTACT

C

Chiara Zingaretti

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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