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临床试验/NCT04903548
NCT04903548已完成不适用

Evaluating the Effects of Segmental/Super Selective Treatment Utilizing Flex-dosing in Treating Unresectable HCC With Y90 SIR-Spheres

Methodist Health System1 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2021年1月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1
试验地点
1
主要终点
Patient demographics

研究概览

简要总结

The overall objective of this research study is to evaluate outcomes associated with flex-dosing in Y90 SIR-Sphere administration in a prospective cohort of unresectable HCC patients eligible for segmental/super selective treatment at Methodist Dallas Medical Center (MDMC).

详细描述

The overall objective of this research study is to evaluate outcomes associated with flex-dosing in Y90 SIR-Sphere administration in a prospective cohort of unresectable HCC patients eligible for segmental/super selective treatment at Methodist Dallas Medical Center (MDMC).

This study will enable physicians to be more precise in administering the correct radio-embolic dose, which will improve safety and efficacy of treatment while maintaining optimal dosing for tumor side effects. This study could potentially identify tumors earlier in the course of disease progression, which may result in more efficacious treatment and quality of life for patients. Earlier diagnosis and treatment may result in decreased costs.

This is a prospective cohort registry study. The prospective study cases will include all eligible Y90 patients, who meet the inclusion criteria who are treated beginning in May 2020 to May 2022. Follow-up of patients included in study will continue as needed in order to evaluate survival outcomes.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 years or older
  • All patients diagnosed with unresectable HCC in two of fewer hepatic segments at MDMC who undergo at least one SIRT procedure with Y-90 resin microspheres (SIR-Spheres®, Sirtex Medical Limited, Sydney, Australia) will be included in data capture. HCC is considered unresectable if it is multifocal or bilobar, or if the patient has malignant portal vein thrombosis, portal hypertension, or decompensated liver disease (Child-Pugh B or C).
  • Eligible cases for inclusion are those that would have undergone Y-90 resin SIRT and had an Eastern Cooperative Oncology Group (ECOG) performance status score of 0 to 2; platelets >60,000; creatinine <2 mg/dL; bilirubin <2 mg/dL; and international normalized ratio (INR) <1.2.

排除标准

  • Subjects that do not meet the inclusion criteria
  • Patients are not eligible for SIRT if they had any extrahepatic disease; contraindication to hepatic artery catheterization such as vascular abnormalities, bleeding diathesis, allergy to contrast dye, concurrent malignancy, refractory ascites, previous external beam radiation, or evidence of any uncorrectable flow to the gastrointestinal tract; or greater than 30 Gy of radiation estimated to be delivered to the lung based on angiography or Tc-99 microaggregated albumin scan (shunt fraction of 20% or greater).

结局指标

主要结局

Patient demographics

时间窗: May 2020 - 2022

Patient demographics

Volumes for liver to be treated

时间窗: May 2020 - 2022

liver volume prior to treatment

Lobe/segment to be treated

时间窗: May 2020 - 2022

treatment location

Objective response rate

时间窗: May 2020 - 2022

using modified response evaluation criteria in solid tumors

Tumor volume

时间窗: May 2020 - 2022

volume of tumor prior to treatment

Lung Shunt

时间窗: May 2020 - 2022

Lung shunt presence

Tumor to normal ratio Tumor to Normal ratio prior to greatment

时间窗: May 2020 - 2022

T:N

Hospital-based charges/costs

时间窗: May 2020 - 2022

Hospital-based charges/costs

Overall survival

时间窗: May 2020 - 2022

Overall survival

SPECT CT

时间窗: May 2020 - 2022

for missed Y90 administrations or extrahepatic Y90

Severity of liver disease

时间窗: May 2020 - 2022

Child-Pugh score

Liver synthetic function

时间窗: May 2020 - 2022

ALBI (albumin-bilirubin) score

Progression-free survival

时间窗: May 2020 - 2022

Progression-free survival

Liver function tests

时间窗: May 2020 - 2022

Measurement of Alanine transaminase (ALT), Aspartate transaminase (AST), Alkaline phosphatase (ALP), Albumin and total protein, Bilirubin, Prothrombin time (PT), L-lactate dehydrogenase (LD), Gamma-glutamyltransferase (GGT)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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