1. Transarterial chemoembolization with medium-sized doxorubicin-eluting Callisphere is safe and effective for patients with hepatocellular carcinoma
- Author
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Chunjian Qi, Caoye Wang, Qi Wang, Jianping Gu, Jin-Guo Xia, Zheng-Qiang Yang, Wenhua Chen, and Wei-Zhong Zhou
- Subjects
Adult ,Male ,medicine.medical_specialty ,Carcinoma, Hepatocellular ,Energy science and technology ,lcsh:Medicine ,medicine.disease_cause ,Gastroenterology ,Article ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,0302 clinical medicine ,Ischemic hepatitis ,Internal medicine ,medicine ,Carcinoma ,Humans ,Chemoembolization, Therapeutic ,Adverse effect ,lcsh:Science ,Response Evaluation Criteria in Solid Tumors ,Aged ,Retrospective Studies ,Multidisciplinary ,Antibiotics, Antineoplastic ,business.industry ,lcsh:R ,Liver Neoplasms ,Common Terminology Criteria for Adverse Events ,Middle Aged ,medicine.disease ,Prognosis ,Microspheres ,Doxorubicin ,030220 oncology & carcinogenesis ,Hepatocellular carcinoma ,lcsh:Q ,Female ,business ,Progressive disease ,Biomarkers ,Liver abscess ,Follow-Up Studies - Abstract
The study aimed to compare the tumor response to and complications of doxorubicin-eluting CalliSphere bead-transarterial chemoembolization (DEB-TACE) using small- and medium-sized beads in patients with hepatocellular carcinoma (HCC) who underwent multiple rounds of oncology therapies. Sixty patients with intermediate stage HCC who had previously received multiple oncology therapies underwent DEB-TACE with CalliSpheres of 100–300 μm (small bead group, n = 34) or 300–500 μm (medium bead group, n = 26) in diameter between October 2016 and December 2018. Adverse events and the response rate of the index tumor based on the modified Response Evaluation Criteria in Solid Tumors at 3 months post-TACE were compared between the groups. The rates of complete response, partial response, stable disease, and progressive disease were 35.4%, 29.4%, 17.6%, and 17.6%, respectively, for the small bead group and 33.1%, 23.1%, 20.8%, and 23.0%, respectively, for the medium bead group, showing no significant between-group differences (P > 0.05). Common Terminology Criteria for Adverse Events version 4.0 grade 3/4 adverse events were reported in 8 patients in the small bead group and in no patients in the medium bead group, showing a significant group difference (P
- Published
- 2019