Actively Recruiting

Phase 2
Phase 3
Age: 18Years +
All Genders
NCT04143516

Tissue Analysis After Tumor Ablation for Liver Metastases Leading to Immediate Retreatment

Led by Memorial Sloan Kettering Cancer Center · Updated on 2026-03-19

200

Participants Needed

1

Research Sites

361 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will see whether collecting and analyzing needle biopsy samples from cancer liver metastases after a tumor ablation procedure will be able to identify cancer cells that are still alive. The results of these biopsies could help determine the next treatment for your cancer, but the biopsies could cause side effects.

CONDITIONS

Official Title

Tissue Analysis After Tumor Ablation for Liver Metastases Leading to Immediate Retreatment

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of liver metastases from various primary tumors
  • Confined liver disease or limited extrahepatic disease stable or controlled for at least 4 months
  • Lesions 3 cm or smaller in maximum diameter
  • At least one FDG-avid lesion to be treated
  • INR less than 1.5
  • Platelet count of 50,000 or higher
Not Eligible

You will not qualify if you...

  • Age under 18 years
  • Less than 5 mm distance to a structure (GI or biliary tract) that cannot be protected from ablation injury
  • INR greater than 1.5 that cannot be corrected with fresh frozen plasma
  • Platelet count under 50,000 that cannot be corrected with transfusion
  • More than 3 tumors in the liver
  • More than 5 tumors of extrahepatic disease
  • Presence of any peritoneal carcinomatosis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Memorial Sloan Kettering Cancer Center

New York, New York, United States, 10065

Actively Recruiting

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Research Team

C

Constantinos Sofocleous, MD, PhD

CONTACT

E

Efsevia Vakiani, MD,PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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