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Completed

NCT Number: NCT05250895

BOLD MRI and FMISO PET for the Assessment of Hypoxic Tumor Microenvironment in Patients with Oligometastatic Liver Cancer Undergoing Yttirum-90 Selective Internal Radiation Therapy

This early phase I trial evaluates the use of hypoxia (lack of oxygen) as a measure in determining the outcome of Y90 selective internal radiation therapy in patients with liver cancer that has spread to a limited number of sites (oligometastatic). Radioembolization with Y90 is a minimally invasive procedure that combines embolization and radiation therapy to treat metastatic liver cancer. Tiny beads filled with radioactive isotope Y-90 are placed inside the blood vessel that provide blood supply to the tumor. This will block the blood flow to the tumor cells while providing a high radiation dose without harming healthy normal tissue.

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Key information

About this study

PRIMARY OBJECTIVE:

I. To investigate the variability of hypoxia in hepatocellular carcinoma (HCC) as quantified by blood oxygen level-dependent (BOLD) magnetic resonance imaging (MRI) and dynamic 18F-Fluoromisonidazole (FMISO) positron emission tomography (PET).

SECONDARY OBJECTIVES:

I. Investigate whether hypoxia, as quantified by BOLD MRI, dynamic FMISO PET, HIF-1alpha and VEGF expression, predicts HCC response to yttrium-90 (Y90) selective internal radiation therapy (SIRT).

II. Assess whether hypoxia quantification by BOLD MRI, dynamic FMISO, HIF-1alpha or VEGF expression individually or in combination more accurately predict the degree of HCC tumor response to Y90 SIRT.

III. Compare the tumor dose response threshold between hypoxic and non-hypoxic HCCs treated with Y90 SIRT.

OUTLINE:

Patients receive 18F-fluoromisonidazole intravenously (IV) and undergo PET and dynamic contrast enhanced (DCE) MRI within 30 days before beginning Y90 SIRT. Patients undergo Y90 SIRT per standard of care.

After completion of study intervention, patients are followed up at 90 days, and then every 12 weeks thereafter.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age >= 18 years
  • Established HCC diagnosis, unilobar or bilobar disease
  • At least 1 tumor >= 3 cm
  • Oligometastatic disease
  • Barcelona Clinic Liver Cancer (BCLC) stage A, B or C
  • Eastern Cooperative Oncology Group (ECOG) performance status =< 2 (Karnofsky >= 60%)
  • Life expectancy > 12 weeks as determined by the Investigator
  • The effects of Y90 Radioembolization on the developing human fetus are unknown. For this reason, female of child-bearing potential (FCBP) must have a negative serum or urine pregnancy test prior to starting therapy
  • FCBP and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately
  • A female of childbearing potential (FCBP) is a sexually mature woman who: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months

Exclusion criteria

  • Patients who are definite transplant candidates
  • Concurrent second malignancy outside of the liver
  • Infiltrative liver tumor
  • Previous liver-directed therapy to targeted tumors
  • BCLC stage D
  • Bilirubin > 2 mg/dL for lobar treatment and bilirubin > 3 mg/dL for segmental or bi-segmental Y90-SIRT
  • Albumin < 3 g/dL
  • Projected lung dose of > 30 Gy in a single session to the liver after prospective treatment planning
  • Body mass index (BMI) > 40

Treatment and study plan

18F-fluoromisonidazole

Other

Given IV

Other names: 18F-MISO, 18F-Misonidazole, FMISO

Biopsy

Procedure

Undergo biopsy

Other names: BIOPSY_TYPE, Bx

Dynamic Contrast-Enhanced Magnetic Resonance Imaging

Procedure

Undergo DCE MRI

Other names: DCE, DCE MRI, DCE-MRI, DYNAMIC CONTRAST ENHANCED MRI

Positron Emission Tomography

Procedure

Undergo PET

Other names: Medical Imaging, Positron Emission Tomography, PET, PET Scan, Positron Emission Tomography Scan, Positron-Emission Tomography, proton magnetic resonance spectroscopic imaging

Primary outcomes

  1. To investigate the variability of hypoxia in HCC at baseline as quantified by BOLD MRI

    Time frame: From weeks 1-2 up to 1 year

    Threshold <1.0 R2 tumor to normal ratio (no unit) as a cutoff for hypoxia

  2. To investigate the variability of hypoxia in HCC at baseline as quantified by immunohistochemistry

    Time frame: From weeks 1-2 up to 1 year

    The staining intensity will be measured and scored with four scales: no staining=0, weak staining=1, moderate staining=2, and strong staining=3. The final staining score will be obtained by stained stumor area% x positive tumor cells % x staining intensity. The tumors will be then categorized as hypoxic (scores 8 to 16) vs. non-hypoxic (scores 0 to 7) (no units).

Secondary outcomes

  1. Determine whether hypoxia is predictor of response in HCC treated with Y90 SIRT

    Time frame: From week 0 up to 1 year

    Treatment Response Assessment using mRECIST

  2. Treatment response

    Time frame: From week 0 Up to 1 year

    Assessed using modified Response Evaluation Criteria in Solid Tumors.

Sponsors and collaborators

Lead sponsor

Emory University

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

Molecular Imaging of the Hypoxic Tumor Microenvironment to Predict Response to Yttirum-90 Selective Internal Radiation Therapy in Hepatocellular Carcinoma- Pilot Study

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Feb 22, 2022
Registry last updated
Mar 13, 2025

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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