RECRUITING

Study of Personalized Cancer Therapy to Determine Response and Toxicity

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is to learn more about personalized cancer therapy including response to treatment and side effects. Information about the tests and treatments a person received, or will receive, for their cancer will be collected from medical records to help the researchers determine whether or not patients respond better when their physicians choose to treat them according to the genetic makeup of their tumor. Optional research tests may be performed on tissue, body cavity fluid, blood or urine provided, discarded biological samples taken during routine care that would normally be disposed of and not saved, or on blood samples collected for this study. These research tests will be used to create a "profile" of the collected specimens which will describe unique characteristics about the genes involved in a person's cancer. The tests will also help researchers look for biomarkers that may help predict how people respond to treatment.

Official Title

UCSD Profile Related Evidence Determining Individualized Cancer Therapy (UCSD PREDICT)

Quick Facts

Study Start:2013-09-05
Study Completion:2026-09-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT02478931

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:7 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Must be willing to provide informed consent, parent permission, or assent
  1. * Subjects unable to give informed consent, parent permission, or assent

Contacts and Locations

Study Contact

Lee Suzanna, MPH
CONTACT
(858) 534-1306
sml012@health.ucsd.edu
Michaela Doering, BS
CONTACT
(858) 657-7512
mdoering@health.ucsd.edu

Principal Investigator

Shumei Kato, MD
PRINCIPAL_INVESTIGATOR
University of California, San Diego

Study Locations (Sites)

UCSD Moores Cancer Center
La Jolla, California, 92093
United States
Eisenhower Medical Center, Lucy Curci Cancer Center
Rancho Mirage, California, 92270
United States
Rady Children's Hospital, San Diego
San Diego, California, 92123
United States

Collaborators and Investigators

Sponsor: Shu Mei Kato

  • Shumei Kato, MD, PRINCIPAL_INVESTIGATOR, University of California, San Diego

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2013-09-05
Study Completion Date2026-09-05

Study Record Updates

Study Start Date2013-09-05
Study Completion Date2026-09-05

Terms related to this study

Additional Relevant MeSH Terms

  • Cancer