2014
DOI: 10.1097/coc.0b013e31827b45f9
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Axitinib for the Treatment of Metastatic Renal Cell Carcinoma

Abstract: Axitinib is a novel, oral, multitargeted tyrosine kinase inhibitor, which inhibits vascular endothelial growth factor receptors 1, 2, and 3 at subnanomolar concentrations in vitro. In the phase III clinical trial in patients with metastatic renal cell carcinoma, axitinib showed a high objective response rate, and significantly prolonged progression-free survival compared with sorafenib. Thus, it is the first drug that has proven the concept of sequencing tyrosine kinase inhibitors in second-line treatment in a… Show more

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Cited by 21 publications
(3 citation statements)
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“…Axitinib is associated with the well-known chronic VEGFR-TKI toxicity, most commonly diarrhea, hypertension, fatigue, hypothyroidism, hand-foot syndrome (palmar-plantar erythrodysaesthesia syndrome) and gastrointestinal side effects (nausea, loss of appetite, etc.) [15,16]. For ICIs, however, the main focus is on immune-mediated side effects.…”
Section: Side Effects and Quality Of Lifementioning
confidence: 99%
“…Axitinib is associated with the well-known chronic VEGFR-TKI toxicity, most commonly diarrhea, hypertension, fatigue, hypothyroidism, hand-foot syndrome (palmar-plantar erythrodysaesthesia syndrome) and gastrointestinal side effects (nausea, loss of appetite, etc.) [15,16]. For ICIs, however, the main focus is on immune-mediated side effects.…”
Section: Side Effects and Quality Of Lifementioning
confidence: 99%
“…When I use axitinib as a monotherapy in the refractory setting, the common toxicities are well-established toxicities for patients getting these VEGFR TKIs. That includes diarrhea, hypertension, fatigue, nausea, and vomiting [ 21 , 22 ]. And it really is important to understand the monotherapy toxicity because we're here today really to talk about the combination of toxicities.…”
Section: Axitinib Safety and Dose Modification (08:08–10:15)mentioning
confidence: 99%
“…Clinical application of molecular targeted therapy has been the first-line option for metastatic RCC since the beginning of this century [1]. Although median progression-free survival is reportedly 6–11 months with molecular targeted therapy, compared with 5–6 months with the previously dominant immunotherapy, molecular targeted therapy remains palliative [2]. Metastatic RCC cells can reach the head and neck area via normal hematogenous flow.…”
Section: Discussionmentioning
confidence: 99%