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

Clinical Outcomes and Quality of Life After Transarterial Radioembolization With Yttrium-90 (TARE-Y90) in Children, Adolescents, and Young Adults With Liver Tumors

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04315883
Enrollment
3
Registered
2020-03-20
Start date
2021-02-11
Completion date
2024-03-28
Last updated
2024-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatoblastoma, Hepatocellular Carcinoma, Rhabdoid Tumor of Liver, Undifferentiated (Embryonal) Sarcoma of the Liver, Pediatric Liver Cancer, Liver Tumors

Keywords

Hepatoblastoma, Hepatocellular carcinoma, Rhabdoid tumor of the liver, Undifferentiated sarcoma of the liver, Liver transplant, unresectable, yttrium 90, Y90, radioembolization, resection, pediatric, cancer, liver tumor

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

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

Interventions

BEHAVIORALQuality 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

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

Sponsors

Alfred I. duPont Hospital for Children
CollaboratorOTHER
Nemours Children's Clinic
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Years to 21 Years
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.

Design outcomes

Primary

MeasureTime frameDescription
Determine the impact of TARE-Y90 treatment on health related quality of life (HRQOL)Assessed at baseline/time of treatmentEvaluation 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
Evaluate the efficacy and clinical utility of TARE-Y90 by examining 2 year survivalPatients will be assessed at 2 years post therapyDeliver catheter directed yttrium-90 directly to liver tumors and assess -Progression Free Survival - Local and Metastatic \-
Evaluate the efficacy and clinical utility of TARE-Y90 by examining 5 year survivalPatients will be assessed at 5 years post therapyDeliver catheter directed yttrium-90 directly to liver tumors and assess -Progression Free Survival - Local and Metastatic
Evaluate the efficacy and clinical utility of TARE-Y90 by examining local tumor responsePatients will be assessed at the end of treatment which is typically 2-4 months following treatmentDeliver 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).
Evaluate the efficacy and clinical utility of TARE-Y90 by examining resection ratePatients 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
Evaluate the efficacy and clinical utility of TARE-Y90 by examining Transplant ratePatients 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
Evaluate the efficacy and clinical utility of TARE-Y90 by examining histologic responsePatients 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
Evaluate the efficacy and clinical utility of TARE-Y90 by examining biologic responsePatients 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
Evaluate the efficacy and clinical utility of TARE-Y90 by examining clinical coursePatients 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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026