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PET-CT for Liver Cancer
N/A
Waitlist Available
Led By Joshua Meyer, MD
Research Sponsored by Fox Chase Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Study Summary
This trial looks at how well PET-CT works in finding the right dose of radiation for patients with liver cancer.
Eligible Conditions
- Liver Cancer
- Cholangiocarcinoma
- Solid Tumors
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Local control
Radiation dose to 70% of the tumor volume, evaluated using PET-CT
Secondary outcome measures
Ability of PET-CT to reproducibly determine dose to tumor, normal liver, and other surrounding organs
Change in dose measured by PET-CT scan
Distribution of activity measured by PET-CT
+2 moreSide effects data
From 2017 Phase 2 trial • 14 Patients • NCT0143748864%
Fatigue
43%
Diarrhea
36%
Constipation
36%
Anemia
36%
Nausea
21%
Creatinine Increased
21%
Lightheadedness
21%
Vomiting
21%
Hypokalemia
14%
Abdominal Pain
14%
Back Pain
14%
Dizziness
14%
Fever
14%
Flu-Like symptoms
14%
Hypomagnesia
14%
Pinching sensation around port
14%
Shortness of Breath
14%
URI
14%
Abdominal cramping
14%
Insomnia
14%
Thrombocytopenia
7%
Dry Skin
7%
Decreased Appetite
7%
Bloating
7%
Sacral Edema
7%
Tinnitus
7%
Blood in Bilirubin increased
7%
Tearing
7%
Acid Reflux
7%
INR increased
7%
Embolic stroke
7%
Pulmonary Embolism
7%
Anorexia
7%
Anxiety
7%
Dyspnea
7%
Dysuria
7%
Fall
7%
Flatulence
7%
Foot Pain
7%
Hematoma
7%
Leg pain
7%
Loose Stools
7%
mild-mod Congestion
7%
Neutrophil count decreased
7%
Neuropathy
7%
Rib pain
7%
Throat discomfort
7%
Urinary incontinence
7%
Urinary Tract Obstruction
7%
Worsening pain
7%
Vision changes
7%
Hypoxia
7%
Abdominal distention
7%
Alkalosis
7%
Bladder Spasm
7%
Blurred Vision
7%
Bone Pain
7%
Cabazitaxel Infusion reaction
7%
Change in Taste
7%
Epigastric Pain
7%
Hematuria
7%
Hypophosphatemia
7%
Hypertension
7%
Pain in Pelvis
7%
Paresthesia bilateral feet
7%
Perioral numbness
7%
Peripheral Neuropathy
7%
Weakness
7%
Weight loss
7%
Tachycardia
7%
Bleeding Gums
7%
PTT prolonged
7%
Pyelonephritis
7%
Rash
100%
80%
60%
40%
20%
0%
Study treatment Arm
Cabazitaxel
Trial Design
1Treatment groups
Experimental Treatment
Group I: Diagnostic: PET scan - CT scanExperimental Treatment3 Interventions
Patients undergo PET-CT scan before and after standard radioembolization on day 0. A subset of patients undergo PET-CT scan on day 1, 24 hours after the day 0 post-treatment PET-CT.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
CT Scan
2016
Completed Phase 2
~570
PET scan
2016
Completed Phase 2
~650
hepatic artery embolization
2014
Completed Phase 3
~160
Find a Location
Who is running the clinical trial?
Fox Chase Cancer CenterLead Sponsor
227 Previous Clinical Trials
37,465 Total Patients Enrolled
2 Trials studying Liver Cancer
709 Patients Enrolled for Liver Cancer
Joshua Meyer, MDPrincipal InvestigatorFox Chase Cancer Center
6 Previous Clinical Trials
179 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have cancer that has spread mostly to your liver or is only in your liver. If you have liver cancer or cancer in the bile ducts, you can also participate.You have cancer in your liver that can be treated with a procedure called radioembolization using SIR-spheres or TheraSphere.
Research Study Groups:
This trial has the following groups:- Group 1: Diagnostic: PET scan - CT scan
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are individuals still being enrolled for the trial?
"Unfortunately, according to the clinicaltrials.gov listing, this medical research is not open for recruitment at present despite being first posted in February 2014 and most recently updated in July 2022. However, there are 1,968 other studies that are actively seeking participants right now."
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