选择性内照射治疗
医学
剂量学
近距离放射治疗
肝细胞癌
放射免疫疗法
核医学
放射治疗
放射科
毒性
内辐射
内科学
抗体
免疫学
单克隆抗体
作者
Alexander Villalobos,Johannes L. du Pisanie,Ripal Gandhi,Nima Kokabi
标识
DOI:10.1055/s-0044-1779715
摘要
As a form of brachytherapy, yttrium-90 radioembolization (Y90-RE), also known as selective internal radiation therapy (SIRT) or trans-arterial radioembolization (TARE), exerts its locoregional tumoricidal effects by its near-pure emission of beta-particles from the radioactive decay of yttrium-90 ([Table 1]). Since its early therapeutic use for the palliative treatment of patients with advanced unresectable hepatocellular carcinoma (HCC), there has been recognition that the tumor response to Y90-RE will be dependent on the relationship between the delivered activity and dose administered. This appreciation for the importance of dosimetry also stemmed from the recognition that liver toxicity can occur due to delivering "too much dose"—specifically, the recognition of radiation-induced liver disease (RILD).[1]
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