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NCT Number: NCT07586046

Defining the Ablative Dose for Y-90 TARE

This study is being done to help doctors improve how they treat liver tumors that cannot be removed by surgery or treated with standard ablation techniques. The researchers want to find out the best amount of radiation that needs to be delivered to completely destroy (or ablate) parts of the liver that have cancer.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Northwestern University

Chicago, Illinois, 60611, United States

Location contact

Amir A Borhani, MD

SUB_INVESTIGATOR

Andrew C Gordon, MD, PhD

CONTACT

[email protected]

(561)703-0134

Andrew C Gordon, MD, PhD

PRINCIPAL_INVESTIGATOR

Cameron Khakpour, BA

CONTACT

[email protected]

312-926-5509

Robert J Lewandowski, MD, FSIR

SUB_INVESTIGATOR

Saad E Abu Zahra, MD

SUB_INVESTIGATOR

About this study

Currently, doctors use Yttrium-90 (Y90) radiation segmentectomy, a treatment that delivers tiny radioactive beads into the blood vessels feeding the liver tumor. These beads give off radiation that helps kill the cancer cells from the inside, right where the tumor is located. This approach allows doctors to target the tumor very precisely, while keeping the rest of the liver as healthy as possible. However, the exact dose needed to fully ablate a tumor without damaging healthy liver tissue is not well established.

To answer this, the study team will use specialized imaging before and after treatment to evaluate how the radiation is distributed in the liver and how the liver responds over time. These include PET/CT or PET/MRI scans, which are standard medical imaging tests that are not considered experimental. During these scans, a small amount of a safe radioactive substance is injected into their vein. This helps show where the Y90 beads are in their liver.

In a PET/CT scan, two types of imaging are performed during the same session. The PET scan detects signals from the radioactive substance and shows how your liver is functioning at a molecular level. The CT scan, which uses x-rays to create detailed cross-sectional images of the body, provides a precise anatomical map that helps localize these functional signals. Together, they give a clear picture of both the structure and activity within the liver.

PET/MRI works similarly but uses magnetic fields and radio waves instead of x-rays. It combines the functional information from the PET scan with the highly detailed soft-tissue images from MRI, which can be especially useful in evaluating the liver. Both imaging techniques are done during a single visit, with the PET component typically performed at the same time as the CT or MRI, depending on which machine is used. They will also have a liver MRI with dual contrast (Eovist and extracellular gadolinium), another standard imaging procedure. MRI uses magnets and radio waves to take detailed pictures of your liver. Eovist is a special dye injected into their vein during the scan that helps highlight liver tissue and shows how well different parts of their liver are functioning. Extracellular gadolinium is a more general contrast agent that enhances blood vessels and tissues, providing complementary information. This helps the doctors confirm whether the tumor area was completely treated.

The goal is to determine the safest and most effective dose of radiation to fully treat cancer while preserving healthy liver tissue. This information may help doctors treat future patients more precisely and safely.

Yttrium-90 and the imaging methods used in this study, including PET/CT, PET/MRI, and dual contrast MRI, are FDA-approved.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of hepatocellular carcinoma (HCC), cholangiocarcinoma, or liver-dominant metastatic disease not amenable to surgical resection or ablation.
  • Age ≥18 years.
  • Tumor size ≤5 cm requiring treatment of ≤2 Couinaud segments.
  • Child-Pugh class A or B liver function
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
  • Adequate organ and bone marrow function as defined below:
  • Leukocytes (WBC) ≥ 3,000/mcL
  • Absolute neutrophil count (ANC) ≥ 1,500/mcL
  • Hemoglobin ≥ 9 g/dL
  • Platelets ≥ 50,000/mcL
  • Total bilirubin ≤ 3.0 mg/dL
  • AST ≤ 100 U/L, ALT ≤ 120 U/L
  • Creatinine ≤ 2.0 mg/dL or estimated GFR ≥ 40 mL/min/1.73 m²
  • Ability to undergo imaging and laboratory evaluations required by the study.
  • Ability to understand and willingness to sign a written informed consent document.

Exclusion criteria

  • Extrahepatic metastases.
  • Pregnant or breastfeeding individuals.
  • Tumors requiring treatment of more than two Couinaud segments.
  • Known hypersensitivity to gadolinium-based contrast agents.
  • Contraindications to MRI (e.g., incompatible pacemakers, claustrophobia unresponsive to sedation).
  • Coagulopathy or clinical instability precluding angiographic intervention.
  • Prisoners or individuals under legal custody.
  • Adults unable to consent.
  • Individuals under 18 years of age.

Treatment and study plan

Yttrium-90 Radiation Segmentectomy (Y90 RS) using glass microspheres

Other

The objective of this study is to define an optimal "ablative dose" range for Y90 Radiation Segmentectomy that achieves complete sectoral ablation detectable on dual contrast MRI and to determine whether this dose-response relationship differs between cirrhotic and non-cirrhotic patients.

Primary outcomes

  1. Ablative Dose Threshold for Y90 Radiation Segmentectomy

    Time frame: From enrollment to the end of post-treatment Y90 12 month follow up visit

    To prospectively define the "ablative dose" threshold for Y90 Radiation Segmentectomy (RS) using post-treatment PET dosimetry and hepatobiliary phase MRI

  2. Impact of Cirrhosis on Ablative Dose Requirements

    Time frame: From enrollment to enrollment to post-treatment Y-90 12 month follow-up visit

    To determine whether cirrhotic patients require a higher threshold dose for ablation compared to non- cirrhotic patients

Secondary outcomes

  1. Correlation of Y90 Dose with Imaging Biomarkers

    Time frame: Assessed at 1, 4-9, and 12 month follow up visits

    To evaluate the correlation between delivered Y90 dose and imaging biomarkers, including signal loss on hepatobiliary phase MRI, ablative margins, extracellular volume fraction, and perfusion changes

  2. Tumor Response and Time-to-Progression Assessment

    Time frame: From enrollment to end of post-treatment Y-90 12 month follow up visit

    To assess tumor response by mRECIST and determine time to progression (TTP)

  3. Safety and Tolerability of Escalating Y90 Doses

    Time frame: From enrollment to end of post-treatment Y90 12 month follow up visit

    To assess the safety and tolerability of escalating segmental Y90 doses (200- 500 Gy) using Bayesian optimal interval (BOIN) dose-escalation design under Data and Safety Monitoring Committee (DSMC) oversight

Other outcomes

  1. Pathologic Necrosis in Explanted Tumors

    Time frame: From enrollment to end of post-treatment Y90 12 month follow-up visit

    To evaluate complete pathological necrosis in explanted tumors from patients who undergo liver resection or transplantation

  2. Early Imaging Biomarkers for Ablation Success

    Time frame: From enrollment to post-treatment Y90 12 month follow-up visit

    To identify novel early imaging biomarkers (Eovist hepatobiliary phase defects, extracellular volume mapping, perfusion changes) that may serve as surrogates for ablation success

Study contacts

Contact information is provided by the study sponsor or research team.

Andrew C Gordon, MD, PhD

CONTACT

[email protected]

(561)703-0134

Cameron Khakpour, BA

CONTACT

[email protected]

312-926-5509

Sponsors and collaborators

Lead sponsor

Northwestern University

Other

Collaborators

  • Radiological Society of North America
  • Robert H. Lurie Cancer Center

Registry information

Official study title

A Prospective Dose-Escalation Study to Define an Ablative Dose of Yttrium-90 Transarterial Radioembolization Using Advanced Dosimetry and Functional MRI (MARGIN Study)

Acronym: MARGIN

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
May 14, 2026
Registry last updated
May 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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