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Search / Trial NCT04143516

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

Launched by MEMORIAL SLOAN KETTERING CANCER CENTER · Oct 28, 2019

Trial Information

Current as of July 23, 2025

Recruiting

Keywords

Optimizing Tumor Ablation Rapid Tissue Analysis Metabolic Imaging Biomarker Validation Predictive Genetic Signatures 19 332

ClinConnect Summary

This clinical trial is looking at how doctors can better understand liver cancer that has spread from other parts of the body. After a procedure to remove tumors in the liver, the researchers will take small samples of the remaining tissue to check for any living cancer cells. By analyzing these samples, the study aims to find out if they can identify the best next steps for treating the cancer. It’s important to know that while these needle biopsies can provide valuable information, they may also have some side effects.

To participate in this trial, you must be between 65 and 74 years old and have liver metastases from different types of cancer. You should have stable liver disease and not have too many tumors in your liver or other parts of your body. If you join the study, you’ll undergo a biopsy after your tumor ablation, and the results could help guide your future treatment. This trial is currently recruiting participants, and everyone is welcome regardless of gender.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Diagnosis of liver metastases from various primary tumors
  • Confined liver disease or limited extrahepatic disease stable/controlled for at least 4 months (extrahepatic disease amenable to treatment is allowed)
  • Lesions of ≤3 cm in maximum diameter
  • At least one FDG-avid lesion to be treated\*\*\*
  • INR \< 1.5\*
  • Platelet count ≥ 50,000
  • Exclusion Criteria:
  • Age \< 18
  • Less than 5 mm distance to a structure (GI or biliary tract), that cannot be protected from ablation injury with technical modifications such as hydro or air dissection
  • INR \> 1.5 that cannot be corrected with fresh frozen plasma \*\*
  • Platelet count of \<50,000 that cannot be corrected with transfusion
  • More than 3 tumors in the liver
  • More than 5 tumors of extrahepatic disease (including mediastinal nodes and pulmonary nodules, abdominal or other lymph nodes, and bone metastasis)
  • Presence of any peritoneal Carcinomatosis
  • For patients on Coumadin, general clinical guidelines for IR ablation will be followed.
  • For patients with no FDG-PET avid tumors aim 2 of the protocol will not be assessed

About Memorial Sloan Kettering Cancer Center

Memorial Sloan Kettering Cancer Center (MSKCC) is a world-renowned institution dedicated to cancer treatment, research, and education. As a leading clinical trial sponsor, MSKCC focuses on advancing innovative cancer therapies through rigorous scientific investigation and collaboration. The center's multidisciplinary team of experts employs cutting-edge methodologies to design and conduct trials that aim to improve patient outcomes and enhance understanding of cancer biology. With a commitment to translating research findings into clinical practice, MSKCC plays a pivotal role in shaping the future of oncology care and ensuring that patients have access to the latest therapeutic advancements.

Locations

New York, New York, United States

Patients applied

0 patients applied

Trial Officials

Constantinos Sofocleous, MD, PhD

Principal Investigator

Memorial Sloan Kettering Cancer Center

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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