Lenvatinib: Difference between revisions
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In May 2016, the US [[Food and Drug Administration]] (FDA) approved it (in combination with [[everolimus]]) for the treatment of advanced [[renal cell carcinoma]] following one prior anti-angiogenic therapy.<ref name=FDA-rcc/> |
In May 2016, the US [[Food and Drug Administration]] (FDA) approved it (in combination with [[everolimus]]) for the treatment of advanced [[renal cell carcinoma]] following one prior anti-angiogenic therapy.<ref name=FDA-rcc/> |
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The drug is also approved in the US and in the European Union for [[hepatocellular carcinoma]] that cannot be removed surgically in patients who have not received cancer therapy by mouth or injection.<ref name=":0">{{cite web|url=https:// |
The drug is also approved in the US and in the European Union for [[hepatocellular carcinoma]] that cannot be removed surgically in patients who have not received cancer therapy by mouth or injection.<ref name=":0">{{cite web |title=Lenvatinib Price |url=https://emergencydrug.com/generic/lenvatinib-4mg-10mg-capsules-price-cost/ |website=Emergency Drug |publisher=Jaman}}</ref><ref name="fda-Aug-2018" /> |
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==Adverse effects== |
==Adverse effects== |
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Revision as of 10:24, 19 September 2024
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| Clinical data | |
|---|---|
| Trade names | Lenvima, others |
| Other names | E7080 |
| AHFS/Drugs.com | Monograph |
| License data |
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| Pregnancy category |
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| Routes of administration | By mouth |
| ATC code | |
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Bioavailability | 85% (estimated) |
| Protein binding | 98–99% |
| Metabolism | CYP3A4, aldehyde oxidase, non-enzymatic |
| Metabolites | Desmethyl-lenvatinib (M2) and others |
| Elimination half-life | 28 hours |
| Excretion | ~65% feces, 25% urine |
| Identifiers | |
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| CAS Number | |
| PubChem CID | |
| IUPHAR/BPS | |
| DrugBank | |
| ChemSpider | |
| UNII | |
| KEGG | |
| ChEBI | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C21H19ClN4O4 |
| Molar mass | 426.86 g·mol−1 |
| 3D model (JSmol) | |
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Lenvatinib, sold under the brand name Lenvima among others, is an anti-cancer medication for the treatment of certain kinds of thyroid cancer and for other cancers as well. It was developed by Eisai Co. and acts as a multiple kinase inhibitor against the VEGFR1, VEGFR2 and VEGFR3 kinases.[4]
Lenvatinib prices vary based on location, dosage, and insurance coverage. For precise costs, check with local pharmacies and insurance providers.[5]
Medical uses
Lenvatinib is approved (since 2015) for the treatment of differentiated thyroid cancer that is either locally recurrent or metastatic, progressive, and did not respond to treatment with radioactive iodine (radioiodine).[6][7]
In May 2016, the US Food and Drug Administration (FDA) approved it (in combination with everolimus) for the treatment of advanced renal cell carcinoma following one prior anti-angiogenic therapy.[8]
The drug is also approved in the US and in the European Union for hepatocellular carcinoma that cannot be removed surgically in patients who have not received cancer therapy by mouth or injection.[5][9]
Adverse effects
Hypertension (high blood pressure) was the most common side effect in studies (73% of patients, versus 16% in the placebo group), followed by diarrhoea (67% vs. 17%) and fatigue (67% vs. 35%).[7] Other common side effects included decreased appetite, hypotension (low blood pressure), thrombocytopenia (low blood platelet count), nausea, muscle and bone pain.[6]
Interactions
As lenvatinib moderately prolongs QT time, addition of other drugs with this property could increase the risk of a type of abnormal heart rhythm, namely torsades de pointes. No relevant interactions with enzyme inhibitors and inducers are expected.[7]
Pharmacology
Mechanism of action
Lenvatinib acts as a multiple kinase inhibitor. It inhibits the three main vascular endothelial growth factor receptors VEGFR1, 2 and 3, as well as fibroblast growth factor receptors (FGFR) 1, 2, 3 and 4, platelet-derived growth factor receptor (PDGFR) alpha, c-Kit, and the RET proto-oncogene. Some of these proteins play roles in cancerogenic signalling pathways. VEGFR2 inhibition is thought to be the main reason for the most common side effect, hypertension.[6]
Pharmacokinetics
Lenvatinib is absorbed quickly from the gut, reaching peak blood plasma concentrations after one to four hours (three to seven hours if taken with food). Bioavailability is estimated to be about 85%. The substance is almost completely (98–99%) bound to plasma proteins, mainly albumin.[6]
Lenvatinib is metabolized by the liver enzyme CYP3A4 to desmethyl-lenvatinib (M2). M2 and lenvatinib itself are oxidized by aldehyde oxidase (AO) to substances called M2' and M3',[10] the main metabolites in the feces. Another metabolite, also mediated by a CYP enzyme, is the N-oxide M3. Non-enzymatic metabolization also occurs, resulting in a low potential for interactions with enzyme inhibitors and inducers.[6]
Terminal half-life is 28 hours, with about two thirds being excreted via the feces, and one quarter via the urine.[6]
Chemistry
Lenvatinib is used in form of the mesylate salt (CAS number 857890-39-2 ).
History
A phase I clinical trial in cancer patients was performed in 2006.[11] A phase III trial treating thyroid cancer patients started in March 2011.[12]
Lenvatinib was granted orphan drug status for treatment of various types of thyroid cancer that do not respond to radioiodine in the US and Japan in 2012 and in Europe in 2013.[13]
In February 2015, the U.S. FDA approved lenvatinib for treatment of progressive, radioiodine refractory differentiated thyroid cancer.[14] In May 2015, European Medicines Agency (EMA) approved the drug for the same indication.[15]
In May 2016, the FDA approved it (in combination with everolimus) for the treatment of advanced renal cell carcinoma following one prior anti-angiogenic therapy.[8]
In August 2018, the FDA approved lenvatinib for the first-line treatment of people with unresectable hepatocellular carcinoma (HCC).[9]
References
- ^ "Prescription medicines: registration of new chemical entities in Australia, 2016". Therapeutic Goods Administration (TGA). 21 June 2022. Retrieved 10 April 2023.
- ^ "Health Canada New Drug Authorizations: 2015 Highlights". Health Canada. 4 May 2016. Retrieved 7 April 2024.
- ^ "Kisplyx EPAR". European Medicines Agency. 25 August 2016. Retrieved 7 January 2024.
- ^ Matsui J, Funahashi Y, Uenaka T, Watanabe T, Tsuruoka A, Asada M (September 2008). "Multi-kinase inhibitor E7080 suppresses lymph node and lung metastases of human mammary breast tumor MDA-MB-231 via inhibition of vascular endothelial growth factor-receptor (VEGF-R) 2 and VEGF-R3 kinase". Clinical Cancer Research. 14 (17): 5459–65. doi:10.1158/1078-0432.CCR-07-5270. PMID 18765537.
- ^ a b "Lenvatinib Price". Emergency Drug. Jaman.
- ^ a b c d e f Haberfeld H, ed. (2015). Austria-Codex (in German). Vienna: Österreichischer Apothekerverlag.
- ^ a b c FDA Professional Drug Information for Lenvima.
- ^ a b "Lenvatinib in combination with Everolimus". U.S. Food and Drug Administration (FDA). 16 May 2016.
- ^ a b "FDA approves lenvatinib for unresectable hepatocellular carcinoma". U.S. Food and Drug Administration (FDA). 16 August 2018. Retrieved 2018-08-16.
- ^ a b Inoue K, Mizuo H, Kawaguchi S, Fukuda K, Kusano K, Yoshimura T (August 2014). "Oxidative metabolic pathway of lenvatinib mediated by aldehyde oxidase". Drug Metabolism and Disposition. 42 (8): 1326–33. doi:10.1124/dmd.114.058073. PMID 24914245. S2CID 206497491.
- ^ Glen H, Boss D, Evans TR, Roelvink M, et al. (2007). "A phase I dose finding study of E7080 in patients (pts) with advanced malignancies". Journal of Clinical Oncology, ASCO Annual Meeting Proceedings Part I. 25 (18S): 14073. Archived from the original on 2012-02-24. Retrieved 2009-09-02.
- ^ Clinical trial number NCT01321554 for "A Trial of E7080 in 131I-Refractory Differentiated Thyroid Cancer" at ClinicalTrials.gov
- ^ "Phase III trial shows lenvatinib meets primary endpoint of progression free survival benefit in treatment of radioiodine-refractory differentiated thyroid cancer" (PDF). Eisai. 3 February 2014.
- ^ U.S. Food and Drug Administration. Hematology/Oncology (Cancer) Approvals & Safety Notifications. [1]
- ^ "Summary of the European public assessment report (EPAR) for Lenvima". European Medicines Agency. 17 September 2018. Archived from the original on 20 June 2018. Retrieved 9 January 2016.
