Yttrium-90 (TARE-Y90) in Children, Adolescents, and Young Adults With Liver Tumors

Sponsor
Nemours Children's Clinic (Other)
Overall Status
Recruiting
CT.gov ID
NCT04315883
Collaborator
Alfred I. duPont Hospital for Children (Other)
15
2
107
7.5
0.1

Study Details

Study Description

Brief Summary

This study will be performed to evaluate the Clinical Outcomes and Quality of Life after Transarterial Radioembolization with Yttrium-90 (TARE-Y90) in Children, Adolescents, and Young Adults with Liver Tumors. The treatment and techniques used here are well established in adults.

The purpose of this study is to evaluate:
  1. the response to treatment and clinical outcomes of treatment with TARE Y-90 as part of standard therapy and

  2. to assess the change in the patient's quality of life before, during and after treatment with TARE-Y90

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Quality of Life Assessment
  • Radiation: Transarterial Radioembolization

Detailed Description

  • Referral to Nemours Liver Tumor Program is made by the primary team (oncologist/surgeon).

  • Phone discussion between the Nemours Liver Tumor Program Team will occur with the referring team about the patient.

  • Phone call between the Nemours Liver Tumor Program Team and the family will occur prior to any visit to discuss the potential plan of care and the basics of the TARE-Y90 procedure and the Quality of Life surveys.

Review of medical records provided by referring institution will be done by the Nemours Liver

Tumor Program Team including:

History, Scans-actual imaging required, Path report-slide submission required, Roadmaps, Labs, Other pertinent medical history and records

-Visit to Nemours/AI DuPont Children's Hospital for initial consultation will be arranged by the Nemours Liver Tumor Program Team.

The patient and family will meet with the team including:

Liver transplant surgeon (Dr Dunn), Interventional Radiologist (Dr Aguado), Social worker, Child life specialist, Pediatric oncologist (Dr Gresh - on site, Dr Katzenstein by telemedicine)

  • Attempt will be made to schedule the pre-planning angiogram as part of initial visit (2nd day of visit). The angiogram requires the following 3-4 hours (mapping of blood vessels in and around tumor - determines whether patient can receive Y90, Angiogram is done with the patient sedated and having been after midnight the night before, The patient is expected to be discharged on the same day of the angiogram- no admit is planned but occasionally the patient may need overnight observation to occur due to age of the patient or the length of the procedure.

  • Return to home.

  • Potential additional single cycle of chemotherapy may be given prior to return to Nemours for Y90.

All further Chemotherapy Care is coordinated with Nemours Liver Tumor oncologists

-A 2nd visit to AIDHC will occur for TARE-Y90 treatment: The procedure lasts about 2-3 hours. There is no planned admit but possible if any problems occur.

  • 2 weeks post procedure a phone call follow-up after treatment will occur with the Nemours team

  • 2 weeks post procedure the patient may resume chemotherapy when cleared by the Nemours team

  • 4-6 weeks post Y90 treatment - a repeat CT/MRI will be done as well as lab tests.

  • If possible, the CT/MRI to be done at AIDHC/Nemours but can be done locally if travel barriers exist.

  • If the tumor is now resectable, planning will be made for resection at AIDHC/Nemours.

  • Evaluation and change of HRQOL survey responses will be performed at baseline (time of treatment) and 1, 6, 12 months and 5 years post-treatment. These surveys will be done by phone, mail or email. Responses will be captured and entered into a REDCAP database

Study Design

Study Type:
Observational
Anticipated Enrollment :
15 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Clinical Outcomes and Quality of Life After Transarterial Radioembolization With Yttrium-90 (TARE-Y90) in Children, Adolescents, and Young Adults With Liver Tumors
Anticipated Study Start Date :
Apr 1, 2020
Anticipated Primary Completion Date :
Mar 1, 2029
Anticipated Study Completion Date :
Mar 1, 2029

Arms and Interventions

Arm Intervention/Treatment
Standard Treatment

Evaluation of change of HRQOL survey responses will be performed: at baseline (time of treatment) and 1 month post treatment 6 months post treatment 12 months post treatment 5 years post-treatment The HRQOL will be done by phone, mail or email. Responses will be captured and entered into a REDCAP database

Behavioral: Quality of Life Assessment
Evaluation of change of HRQOL survey responses will be performed: at baseline (time of treatment) and 1 month post treatment 6 months post treatment 12 months post treatment 5 years post-treatment The HRQOL will be done by phone, mail or email. Responses will be captured and entered into a REDCAP database

Radiation: Transarterial Radioembolization
Deliver catheter directed yttrium-90 directly to liver tumors and assess -Progression Free Survival - Local and Metastatic Local Tumor Response by calculating the decreases in tumor size and enhancement after treatment. This will be assessed by modified Response Evaluation Criteria for Solid Tumors (mRECIST). Resection Rate following treatment Transplant Rate following treatment Histologic Response by assessing tumor histopathology in patients who undergo tumor resection or liver transplant Biologic Response by monitoring serum tumor markers (e.g. alphafetoprotein-AFP) in AFP secreting tumors Review of clinical course post-treatment-rehospitalization rate

Outcome Measures

Primary Outcome Measures

  1. Determine the impact of TARE-Y90 treatment on health related quality of life (HRQOL) [Assessed at baseline/time of treatment]

    Evaluation of change of HRQOL survey responses will be performed: -at baseline (time of treatment) The HRQOL will be done by phone, mail or email. Responses will be captured and entered into a REDCAP database

  2. Determine the impact of TARE-Y90 treatment on health related quality of life (HRQOL) [Assessed at 1 month post therapy]

    Evaluation of change of HRQOL survey responses will be performed: - 1 month post treatment The HRQOL will be done by phone, mail or email. Responses will be captured and entered into a REDCAP database

  3. Determine the impact of TARE-Y90 treatment on health related quality of life (HRQOL) [Assessed at 6 months post therapy]

    Evaluation of change of HRQOL survey responses will be performed: - 6 months post treatment The HRQOL will be done by phone, mail or email. Responses will be captured and entered into a REDCAP database

  4. Determine the impact of TARE-Y90 treatment on health related quality of life (HRQOL) [Assessed at 12 months post therapy]

    Evaluation of change of HRQOL survey responses will be performed: - 12 months post treatment The HRQOL will be done by phone, mail or email. Responses will be captured and entered into a REDCAP database

  5. Determine the impact of TARE-Y90 treatment on health related quality of life (HRQOL) [Assessed at 5 years post therapy]

    Evaluation of change of HRQOL survey responses will be performed: - 5 years post-treatment The HRQOL will be done by phone, mail or email. Responses will be captured and entered into a REDCAP database

  6. Evaluate the efficacy and clinical utility of TARE-Y90 by examining 2 year survival [Patients will be assessed at 2 years post therapy]

    Deliver catheter directed yttrium-90 directly to liver tumors and assess -Progression Free Survival - Local and Metastatic -

  7. Evaluate the efficacy and clinical utility of TARE-Y90 by examining 5 year survival [Patients will be assessed at 5 years post therapy]

    Deliver catheter directed yttrium-90 directly to liver tumors and assess -Progression Free Survival - Local and Metastatic

  8. Evaluate the efficacy and clinical utility of TARE-Y90 by examining local tumor response [Patients will be assessed at the end of treatment which is typically 2-4 months following treatment]

    Deliver catheter directed yttrium-90 directly to liver tumors and assess -Local Tumor Response by calculating the decreases in tumor size and enhancement after treatment. This will be assessed by modified Response Evaluation Criteria for Solid Tumors (mRECIST).

  9. Evaluate the efficacy and clinical utility of TARE-Y90 by examining resection rate [Patients will be assessed at the end of treatment which is typically 2-4 months following treatment.]

    Deliver catheter directed yttrium-90 directly to liver tumors and assess -Resection Rate following treatment

  10. Evaluate the efficacy and clinical utility of TARE-Y90 by examining Transplant rate [Patients will be assessed at the end of treatment which is typically 2-4 months following treatment.]

    Deliver catheter directed yttrium-90 directly to liver tumors and assess -Transplant Rate following treatment

  11. Evaluate the efficacy and clinical utility of TARE-Y90 by examining histologic response [Patients will be assessed at the end of treatment which is typically 2-4 months following treatment.]

    Deliver catheter directed yttrium-90 directly to liver tumors and assess -Histologic Response by assessing tumor histopathology in patients who undergo tumor resection or liver transplant

  12. Evaluate the efficacy and clinical utility of TARE-Y90 by examining biologic response [Patients will be assessed at the end of treatment which is typically 2-4 months following treatment.]

    Deliver catheter directed yttrium-90 directly to liver tumors and assess -Biologic Response by monitoring serum tumor markers (e.g. alphafetoprotein-AFP) in AFP secreting tumors

  13. Evaluate the efficacy and clinical utility of TARE-Y90 by examining clinical course [Patients will be assessed at the end of treatment which is typically 2-4 months following treatment.]

    Deliver catheter directed yttrium-90 directly to liver tumors and assess -Review of clinical course post-treatment-rehospitalization rate

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 21 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Boys and girls age < 21 years of age

  • History of liver tumor

  • Meet criteria for treatment with TARE-Y90

Exclusion Criteria:
  • • Inability to complete required study procedures.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Nemours-AI duPont Hospital for Children Wilmington Delaware United States 19803
2 Nemours Children's Specialty Care Jacksonville Florida United States 32207

Sponsors and Collaborators

  • Nemours Children's Clinic
  • Alfred I. duPont Hospital for Children

Investigators

  • Principal Investigator: Howard Katzenstein, Nemours

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Howard Katzenstein, Principal Investigator, Nemours Children's Clinic
ClinicalTrials.gov Identifier:
NCT04315883
Other Study ID Numbers:
  • NEMOURS TARE-Y90: ST1901
First Posted:
Mar 20, 2020
Last Update Posted:
Apr 6, 2020
Last Verified:
Apr 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Howard Katzenstein, Principal Investigator, Nemours Children's Clinic
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 6, 2020