Actively Recruiting

All Genders
ID04654975

Risk Factors and Treatment Options for Metachronic Brain Metastases After Esophagectomy for Esophageal Cancer: a Multicentric Retrospective Cohort Study (METABREC)

Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2024-07-03

10000

Participants Needed

8

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying brain metastases that occur after esophagectomy, a key surgical treatment for esophageal cancer. This study aims to understand how often brain metastases happen and what risk factors may contribute to them, especially comparing patients who had primary surgery to those who underwent neoadjuvant treatment followed by surgery. The focus is on patients treated between 2000 and 2019, as brain metastases, though rare, can seriously affect survival and treatment options are often challenging. The study involves analyzing medical records of patients who had esophagectomy for esophageal cancer, including those who received various types of neoadjuvant therapies or primary surgery. Researchers will look at factors such as the number, characteristics, and timing of brain metastases, and compare the odds of developing brain metastases between different treatment approaches. This is a retrospective observational study without any new treatment being administered. Participants' data from 2000 to 2019 will be reviewed to determine outcomes like overall survival, time to cancer recurrence, and specific risk factors for brain metastases. The main measurement is the odds ratio for brain metastasis during this period. The study will also assess the number and features of brain metastases. Since this is a retrospective study, there are no visits or procedures for participants, and no direct interventions or follow-up required.

CONDITIONS

Brief Title

Metachronic Brain Metastases After Esophagectomy for Esophageal Cancer (METABREC)

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients receiving surgical treatment for esophageal cancer between 1 januari 2000 and 31 december 2019
  • Patients who had any neoadjuvant treatment followed by surgery, primary surgery, or salvage surgery
  • Diagnosis of adenocarcinoma or squamous cell carcinoma of the esophagus
Not Eligible

You will not qualify if you...

  • Other histology types besides adenocarcinoma or squamous cell carcinoma
  • Hypopharyngeal carcinoma extending to the esophagus requiring total laryngo-pharyngo-esophagectomy
  • Early esophageal carcinoma classified as cT IS-1a N0 M0
  • Palliative esophagectomy procedures

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

Duration - Up to 20 years (from 2000 to 2020)

Participants who underwent esophagectomy for esophageal cancer are observed to study risk factors and outcomes related to brain metastases.

Visits as per routine clinical follow-up

Trial Site Locations

Total: 8 locations

1

MD Anderson Cancer Center

Houston, Texas, United States, 77030

Not Yet Recruiting

2

Universitair ziekenhuis Gent

Ghent, Belgium

Not Yet Recruiting

3

Centre Hospitalier régional Universitaire de Lille

Lille, France

Not Yet Recruiting

4

Saint James Hospital

Dublin, Ireland

Not Yet Recruiting

5

Amsterdam UMC

Amsterdam, Netherlands

Actively Recruiting

6

Zuyderland MC

Heerlen, Netherlands

Not Yet Recruiting

7

Erasmus MC

Rotterdam, Netherlands

Not Yet Recruiting

8

Karolinska Institutet

Stockholm, Sweden

Actively Recruiting

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Research Team

L

Lieven P Depypere, PhD

J

Johnny Moons, Msc

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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