TY - JOUR
T1 - Evaluating the Effectiveness of Yttrium-90 Glass Microspheres in the Treatment of Hepatocellular Carcinoma, Intrahepatic Cholangiocarcinoma, and Metastatic Colorectal Cancer in Practice
T2 - Protocol for the Prospective PROACTIF Phase IV Registry Study in France
AU - On behalf of PROACTIF registry group
AU - Garin, Etienne
AU - Pinaquy, Jean Baptiste
AU - Bailly, Clement
AU - Sengel, Christian
AU - Mariano-Goulart, Denis
AU - Edeline, Julien
AU - Blanc, Jean Frederic
AU - Bouvier, Antoine
AU - Tordo, Jeremie
AU - Rode, Agnes
AU - Becker, Stéphanie
AU - Sefrioui, David
AU - de Baere, Thierry
AU - Somma, Claude
AU - Mastier, Charles
AU - Goupil, Jean
AU - Chevallier, Patrick
AU - Regnault, Helene
AU - Vibert, Eric
AU - Manfredi, Sylvain
AU - Vicaut, Eric
AU - Patel, Binal
AU - Boucher, Eveline
AU - Guiu, Boris
N1 - Publisher Copyright:
© 2021, Springer Science+Business Media, LLC, part of Springer Nature and the Cardiovascular and Interventional Radiological Society of Europe (CIRSE).
PY - 2022/1/1
Y1 - 2022/1/1
N2 - Primary Objective: Recently, selective internal radiation therapy using yttrium-90 (Y90) glass microspheres (TheraSphere™) was approved for reimbursement by health authorities in France. The PROACTIF study aims to gather data on effectiveness, patient quality of life, and safety with use of Y90 glass microspheres in real-world clinical settings in France. Inclusion Criteria: Patient with a diagnosis of hepatocellular carcinoma (HCC), intrahepatic cholangiocarcinoma (iCC), and/or metastatic colorectal cancer (mCRC) who was treated with a dose of Y90 glass microspheres that has been reimbursed in France and who do not oppose use of their personal medical data. Exclusion Criteria: If data collection is opposed, treatment is reimbursed but not administered, or treatment is administered but not reimbursed. Outcome Measures: Primary outcome measures include overall survival from time of Y90 glass microsphere treatment and quality of life, as assessed using the Functional Assessment of Cancer Therapy- Hepatobiliary questionnaire. Estimated Number of Patients to Be Included: This is an open study and there is no set number of patients; 115 have already been enrolled. Planned Subgroup Analyses: Analyses will be stratified by disease state (HCC, iCC, or mCRC). Subgroups to be analyzed include age group, unilobar/bilobar disease at baseline, Eastern Cooperative Oncology Group (ECOG) status at baseline, liver tumor burden at baseline, target lesion size, and standard versus multi-compartment personalized dosimetry treatment. Planned Recruitment and Observation Period: Recruitment includes patients who are prescribed and treated with a commercial vial of Y90 glass microspheres between 01 January 2019 and 31 December 2024. Trial registration: ClinicalTrials.gov Identifier: NCT04069468.
AB - Primary Objective: Recently, selective internal radiation therapy using yttrium-90 (Y90) glass microspheres (TheraSphere™) was approved for reimbursement by health authorities in France. The PROACTIF study aims to gather data on effectiveness, patient quality of life, and safety with use of Y90 glass microspheres in real-world clinical settings in France. Inclusion Criteria: Patient with a diagnosis of hepatocellular carcinoma (HCC), intrahepatic cholangiocarcinoma (iCC), and/or metastatic colorectal cancer (mCRC) who was treated with a dose of Y90 glass microspheres that has been reimbursed in France and who do not oppose use of their personal medical data. Exclusion Criteria: If data collection is opposed, treatment is reimbursed but not administered, or treatment is administered but not reimbursed. Outcome Measures: Primary outcome measures include overall survival from time of Y90 glass microsphere treatment and quality of life, as assessed using the Functional Assessment of Cancer Therapy- Hepatobiliary questionnaire. Estimated Number of Patients to Be Included: This is an open study and there is no set number of patients; 115 have already been enrolled. Planned Subgroup Analyses: Analyses will be stratified by disease state (HCC, iCC, or mCRC). Subgroups to be analyzed include age group, unilobar/bilobar disease at baseline, Eastern Cooperative Oncology Group (ECOG) status at baseline, liver tumor burden at baseline, target lesion size, and standard versus multi-compartment personalized dosimetry treatment. Planned Recruitment and Observation Period: Recruitment includes patients who are prescribed and treated with a commercial vial of Y90 glass microspheres between 01 January 2019 and 31 December 2024. Trial registration: ClinicalTrials.gov Identifier: NCT04069468.
KW - Hepatocellular carcinoma
KW - Intrahepatic cholangiocarcinoma
KW - Liver metastatic colorectal cancer
KW - Selective internal radiation therapy
KW - Yttrium-90
UR - http://www.scopus.com/inward/record.url?scp=85119399065&partnerID=8YFLogxK
U2 - 10.1007/s00270-021-03002-0
DO - 10.1007/s00270-021-03002-0
M3 - Article
C2 - 34796373
AN - SCOPUS:85119399065
SN - 0174-1551
VL - 45
JO - CardioVascular and Interventional Radiology
JF - CardioVascular and Interventional Radiology
IS - 1
ER -