Английская Википедия:Axitinib
Шаблон:Short description Шаблон:Drugbox
Axitinib, sold under the brand name Inlyta, is a small molecule tyrosine kinase inhibitor developed by Pfizer. It has been shown to significantly inhibit growth of breast cancer in animal (xenograft) models[1] and has shown partial responses in clinical trials with renal cell carcinoma (RCC)[2] and several other tumour types.[3]
It was approved to treat renal cell carcinoma by the U.S. Food and Drug Administration after showing a modest increase in progression-free survival,[4] though there have been reports of fatal adverse effects.[5]
Approvals and indications
Renal cell carcinoma
It has received approval for use as a treatment for renal cell carcinoma from the US Food and Drug Administration (FDA) (27 January 2012), the European Medicines Agency (EMA) (13 September 2012), the UK Medicines and Healthcare products Regulatory Agency (MHRA) (3 September 2012) and the Australian Therapeutic Goods Administration (TGA) (26 July 2012).[6][7][8][9]
Clinical trials
A Phase II clinical trial showed good response in combination chemotherapy with gemcitabine for advanced pancreatic cancer.[10] However, Pfizer reported on January 30, 2009, that Phase III clinical trials of the drug when used in combination with gemcitabine showed no evidence of improved survival rates over treatments using gemcitabine alone for advanced pancreatic cancer and halted the trial.[11]
In 2010, a Phase III trial for previously treated metastatic renal cell carcinoma (mRCC) showed significantly extended progression-free survival when compared to sorafenib.[12] In December 2011, the Oncologic Drugs Advisory Committee (ODAC) voted unanimously to recommend that US FDA approve axitinib for the second-line treatment of patients with advanced renal cell carcinoma (RCC), based on the results of the Phase III trial comparing axitinib and sorafenib.[13]
It has also been studied in combination with the ALK1 inhibitor dalantercept.[14]
A study published in 2015[15] showed that axitinib effectively inhibits a mutated gene (BCR-ABL1[T315I]) that is common in chronic myeloid leukemias and adult acute lymphoblastic leukemias which have become resistant to other tyrosine kinase inhibitors like imatinib. This is one of the first examples of a new indication for an existing drug being discovered by screening known drugs using a patient's own cells.
Adverse effects
Шаблон:See also Diarrhea, hypertension, fatigue, decreased appetite, nausea, dysphonia, hand-foot syndrome, weight decreased, vomiting, asthenia, and constipation are the most common side effects occurring in more than 20% of patients.[16]
Interactions
Coadministration with strong CYP3A4/CYP3A5 inhibitors should be avoided where possible as they may reduce plasma clearance of axitinib.[17]
Mechanism of action
Its primary mechanism of action is thought to be vascular endothelial growth factor receptor 1–3, c-KIT and PDGFR inhibition, this, in turn, enables it to inhibit angiogenesis (the formation of new blood vessels by tumours).[18]
It was also proposed that it might act by inducing autophagy, as some other tyrosine kinase inhibitors, like sorafenib.[19]
It has also been shown[15] to bind (in a different conformation from the VEGF binding) to the BCR-ABL fusion protein, specifically inhibiting the drug-resistant T315I mutant isoform.
Protein | IC50 (nM) |
---|---|
VEGFR1 | 0.1 |
VEGFR2 | 0.2 |
VEGFR3 | 0.1-0.3 |
PDGFR | 1.6 |
c-KIT | 1.7 |
Pharmacokinetics
Bioavailability | Tmax | Cmax | AUC | Vd | Plasma protein binding | Metabolising enzymes | t1/2 | Excretion routes |
---|---|---|---|---|---|---|---|---|
58% | 2.5-4.1 hr | 27.8 ng/mL | 265 ng•h/mL | 160 L | >99% | Mostly CYP3A4 and CYP3A5. Lesser contributions from CYP1A2, CYP2C19, UGT1A1 | 2.5-6.1 hr | Faeces (41%), urine (23%) |
Society and culture
Brand names
In Bangladesh it is under the trade name Axinix.Шаблон:Citation needed span
In Germany, Switzerland and other European countries it is available under the trade name Inlyta.[20][21]
References
External links
Шаблон:Extracellular chemotherapeutic agents Шаблон:Growth factor receptor modulators Шаблон:Portal bar
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- ↑ 15,0 15,1 Шаблон:Cite journal
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- ↑ 17,0 17,1 Ошибка цитирования Неверный тег
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- ↑ AHFS Patient Medication Information [Internet]. Bethesda (MD): American Society of Health-System Pharmacists, Inc.; c2022. Axitinib; [last revised 2020 August 15; cited 2022 March 28]; [about 5 p.]. Available from: https://medlineplus.gov/druginfo/meds/a612017.html
- ↑ Шаблон:Cite web
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