BioPearl™ doxorubicin microspheres for unresectable HCC: a prospective, single-arm, multicenter study: BIOPEARL-ONE

被引:1
|
作者
Verset, Gontran [1 ,2 ]
Iezzi, Roberto [3 ]
Bargellini, Irene [4 ]
Bucalau, Ana-Maria [1 ]
Pereira, Philippe [5 ]
Groezinger, Gerd [6 ]
Spreafico, Carlo [7 ]
Maleux, Geert [8 ]
机构
[1] Univ Libre Bruxelles, Hop Erasme, Dept Gastroenterol Hepatopancreatol & Digest Oncol, Route Lennik 808, B-1070 Brussels, Belgium
[2] Inst Paoli Calmettes, Oncol Marseille, Marseille, Provence Alpes, France
[3] Fdn Policlin Univ Agostino Gemelli IRCCS, Dipartimento Diagnost Immagini Radioterapia Oncolo, UOC Radiol Diagnost Interventist Gen, Rome, Lazio, Italy
[4] Candiolo Canc Inst, Radiodiagnost Dept, Turin, Italy
[5] SLK Kliniken GmbH Heilbronn, Ctr Radiol Minimally Invas Therapies & Nucl Med, Heilbronn, Germany
[6] Univ Tubingen, Dept Radiol Diagnost & Intervent Radiol, Tubingen, Germany
[7] IRCCS Ist Nazl Tumori Milano, IRCCS Fdn, Dept Radiol, Intervent Radiol Unit, Milan, Italy
[8] Univ Hosp Leuven, Radiol, Louvain, Vlaams Brabant, Belgium
关键词
Hepatocellular carcinoma; DEM-TACE; doxorubicin; resorbable microsphere; safety; technical success; efficacy; RANDOMIZED CONTROLLED-TRIAL; DEGRADABLE STARCH MICROSPHERES; HEPATOCELLULAR-CARCINOMA; TRANSARTERIAL CHEMOEMBOLIZATION; DOUBLE-BLIND; TACE;
D O I
10.1080/14796694.2024.2446137
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Drug-eluting microsphere transarterial chemoembolization (DEM-TACE) reduces systemic exposure to chemotherapeutic drugs compared with conventional TACE but permanently occludes the embolized vessels, potentially obviating the possibility of re-treatment with TACE. Temporary embolization by resorbable BioPearl (TM) microspheres might facilitate subsequent re-treatments. We herein describe the trial protocol of BIOPEARL-ONE, a prospective, single-arm, multicenter, post-market clinical follow-up study. The primary objectives are technical success and safety following the use. DEM-TACE with doxorubicin-loaded BioPearl (TM) for unresectable hepatocellular carcinoma (HCC). The secondary objectives are tumor response, duration of response, progression-free survival, and survival rate at 18 months. Fifty patients with HCC nodules smaller than 5 cm and within the up-to-7 criteria will be enrolled. Clinical Trial Registration: NCT05911633
引用
收藏
页码:557 / 564
页数:8
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