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Phase 2 N=101 Randomized Single-blind Treatment

Trial of Beads Versus Doxorubicin Eluting Beads for Arterial Embolization of Hepatocellular Carcinoma

Hepatocellular Carcinoma · Liver Cancer · Hepatoma

Enrolled (actual)
101
Serious AEs
94.1%
Results posted
Aug 2023
Primary outcome: Primary: Response to Treatment by RECIST Criteria — 3; 3; 48; 47 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Bead Block microspheres (Device); Bead + Dox Arm (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Memorial Sloan Kettering Cancer Center
Primary completion
Jun 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Response to Treatment by RECIST Criteria
3; 3; 48; 47
SECONDARY
Number of Participants Evaluated for Toxicity
51; 50
SECONDARY
Progression Free Survival
6.2; 2.8
SECONDARY
Overall Survival
3; 3; 48; 47

Summary

The purpose of this study is to evaluate the effect of blocking the blood vessels to the tumor in your liver with small beads alone (Bead Block) versus blocking them with the same bead that contains and releases doxorubicin (a chemotherapy agent). The reason for the study is to see if adding doxorubicin kills more tumor than would be killed by just blocking the blood supplying the tumor. The chemotherapy, doxorubicin, has been used for many years to treat patients with cancer. This procedure to block the blood vessels is called embolization. Embolization is a common treatment for patients with liver cancer who cannot have surgery. The investigators are comparing the standard treatment (using the small beads alone) with another that should be at least as good, but possibly better (with the addition of the drug, doxorubicin). There is no guarantee that the new treatment is better and it is possible that there might be more side effects (related to the doxorubicin) than what is seen with the standard treatment.

Eligibility Criteria

Inclusion Criteria

  • Patient with a confirmed diagnosis of HCC according to EASL criteria for diagnosis; who is not a surgical resection candidate, or refuses surgery
  • Patient must be 18 years of age or older
  • Patient must be Okuda stage I or II
  • Patient must have an ECOG performance status of 0 or 1
  • No prior chemotherapy or biotherapy within 4 weeks of scheduled embolization, with all toxicities, if any, resolved to grade 3000 cells/mm3
  • ANC > 1500 cells/mm3
  • Negative serum pregnancy test (Female of childbearing potential only)

Exclusion Criteria

  • Patient has another primary tumor, with the exception of conventional basal cell CA, superficial bladder cancer, melanoma in situ, or treated prostate cancer currently without biochemical or radiographic evidence of active disease
  • Women who are pregnant or lactating
  • Patient previously treated with doxorubicin
  • Contraindication to angiography/embolization including: patients who cannot receive contrast 1.Severe allergic reaction to contrast despite pre-medication, 2. poor renal function; 3.Lack of arterial access (eg femoral artery occlusion); 4. other, based on judgment of the investigator
  • Patient has already undergone hepatic arterial embolization for the hepatocellular cancer for which they are currently being evaluated
  • Patient has received prior radiotherapy for the hepatocellular cancer for which they are currently being evaluated
  • Patient has had previous local-regional treatment of the current target tumor volume
  • Patient who cannot have CT scan
  • Patient at very high risk for post-embolization hepatic failure: 1. Child's C cirrhosis, 2. > 75% liver replaced by tumor
  • Cardiac exclusion for: 1. Myocardial infarction within 90 days of study, 2. uncontrolled arrhythmia, 3. LVEF < 50% for patients randomized to receive LC Bead
  • Patients with tumors exhibiting characteristics considered contra-indications to particle embolization, including: 1. collateral vessel pathways potentially endangering normal territories during embolization, 2. arteries supplying tumor not large enough to accept LC Bead or Bead Block, 3. Presence of arterial to systemic venous shunts, 4. Presence of arterial to pulmonary vascular shunts
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00539643). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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