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Skip search results from other journals and go to results- 2 JMIR Research Protocols
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Sunitinib- and sorafenib-associated thyroid dysfunction are time-varying and underreported adverse drug reactions (ADR). Despite the efficacy of multitargeted tyrosine kinase inhibitors TKI as first- or second-line therapies for solid and hematologic cancers, thyroid dysfunction—especially hypothyroidism—may complicate treatment regimens using sunitinib and sorafenib.
JMIR Form Res 2025;9:e67767
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There is more rationale to combine sorafenib with TARE than with TACE. First, TARE is better tolerated than TACE, which may allow a higher dose and longer length of therapy with sorafenib. Additionally, sorafenib may be potentially more synergistic with yttrium-90, as antiangiogenic agents potentiate the effects of radiation on tumor regression [27].
JMIR Res Protoc 2018;7(8):e11234
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Sorafenib is the only systemic therapy shown to confer survival advantages compared with placebo in patients with advanced unresectable HCC. Two phase III randomized controlled trials (RCTs; the Sorafenib Hepatocellular Carcinoma Assessment Randomized Protocol [SHARP] study and the Asia-Pacific trial) showed significant increases in median overall survival (OS) in patients treated with sorafenib, compared with placebo [7,8].
JMIR Res Protoc 2017;6(2):e17
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