⭐️⭐️⭐️⭐️⭐️ "A total no brainer"

⭐️⭐️⭐️⭐️⭐️ "Love this, so easy."

Spots is the easy way to track your skin, mole and cancer changes.

Spots Global Cancer Trial Database for A TheraSphere® Advanced Dosimetry Retrospective Global Study in HCC

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: A TheraSphere® Advanced Dosimetry Retrospective Global Study in HCC

Official Title: A TheraSphere® Advanced Dosimetry Retrospective Global Study Evaluation in Hepatocellular Carcinoma Treatment

Study ID: NCT03295006

Interventions

TheraSphere

Study Description

Brief Summary: This retrospective, multinational, single-arm study will be conducted in at least 8 sites. An interim analysis will be conducted with data from 100 patients with up to 10 well defined HCC tumor(s) and with at least one tumor ≥3 cm. Normal tissue absorbed dose using pre-procedural 99mTc MAA SPECT or SPECT/CT imaging will be measured to allow the mean absorbed normal tissue dose corresponding to a ≤15% probability of CTCAE grade 3 or higher hyperbilirubinemia (in the absence of disease progression) to be calculated. Total bilirubin will be recorded and graded according to CTCAE version 4.02. All dose-related SAEs at 3 months follow-up will be followed until resolution, death or lost-to-follow-up. AEs related to disease progression will not be considered related to TheraSphere.

Detailed Description: Recently published evidence indicates a correlation between yttrium-90 dose delivered to the tumor and normal tissue with safety and efficacy outcomes but there are no validated methods to consistently measure dose delivered to the tumor and normal tissue. In contrast to the standard clinical approach based on average dose to one target volume, this trial, sponsored by Biocompatibles UK, will explore an alternative two-compartment TheraSphere dosimetry methodology to calculate absorbed dose to tumor and normal tissue

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Stanford University Medical Center, Stanford, California, United States

University of Florida College of Medicine, Gainesville, Florida, United States

Northwestern Memorial Hospital, Robert H Lurie Comprehensive Cancer Center, Chicago, Illinois, United States

Indiana University School of Medicine, Indianapolis, Indiana, United States

Washington University in St. Louis, School of Medicine, Saint Louis, Louisiana, United States

The University of Texas MD Anderson Cancer Center, Houston, Texas, United States

Centre Eugene Marquis, Rennes, , France

Universitätsklinikum Essen, Essen, , Germany

Foundation IRCCS Istituto Nazionale Tumori, Milan, , Italy

Universitair Medisch Centrum Utrecht, Utrecht, , Netherlands

King Faisal Hospital, Riyad, , Saudi Arabia

Centre Hospitalier Universitaire Vaudois, Lausanne, , Switzerland

Istanbul university Istanbul medical school, Fatih, , Turkey

Florence Nightingale, Şişli, , Turkey

Contact Details

Name: Marnix Lam, MD, PhD

Affiliation: Universitair Medisch Centrum Utrecht

Role: PRINCIPAL_INVESTIGATOR

Name: Riad Salem, MD

Affiliation: Northwestern University

Role: PRINCIPAL_INVESTIGATOR

Name: Etienne Garin, MD

Affiliation: Centre Eugène Marquis

Role: PRINCIPAL_INVESTIGATOR

Name: Hugo de Jong, PhD

Affiliation: Universitair Medisch Centrum Utrecht

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

Logo

Take Control of Your Skin and Body Changes Today.

Try out Spots for free, set up only takes 2 mins.

spots app storespots app store

Join others from around the world: