Nilotinib

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Nilotinib
Nilotinib2DACS.svg
Nilotinib3Dan.gif
Names
Trade namesTasigna, others
Other namesAMN107
  • 4-methyl-N-[3-(4-methyl-1H-imidazol-1-yl)- 5-(trifluoromethyl)phenyl]-3- [(4-pyridin-3-ylpyrimidin-2-yl) amino]benzamide
Clinical data
Drug classBcr-Abl tyrosine kinase inhibitor[1]
Main usesChronic myelogenous leukemia (CML) which Philadelphia chromosome[2]
Side effectsLow platelets, low white blood cells, anemia, rashes, vomiting, diarrhea, joint pains[1]
Pregnancy
category
  • AU: D
  • US: D (Evidence of risk)
Routes of
use		By mouth
Defined daily dosenot established [3]
External links
AHFS/Drugs.comMonograph
MedlinePlusa608002
Legal
License data
Legal status
Pharmacokinetics
Bioavailability30%[4]
Protein binding98%[4]
MetabolismLiver (mostly CYP3A4-mediated)[4]
Elimination half-life15-17 hours[4]
ExcretionFaeces (93%)[4]
Chemical and physical data
FormulaC28H22F3N7O
Molar mass529.527 g·mol−1
3D model (JSmol)
  • Cc1ccc(cc1Nc2nccc(n2)c3cccnc3)C(=O)Nc4cc(cc(c4)n5cc(nc5)C)C(F)(F)F
  • InChI=1S/C28H22F3N7O/c1-17-5-6-19(10-25(17)37-27-33-9-7-24(36-27)20-4-3-8-32-14-20)26(39)35-22-11-21(28(29,30)31)12-23(13-22)38-15-18(2)34-16-38/h3-16H,1-2H3,(H,35,39)(H,33,36,37) checkY
  • Key:HHZIURLSWUIHRB-UHFFFAOYSA-N checkY

Nilotinib, sold under the brand name Tasigna, is a medication used to treat chronic myelogenous leukemia (CML) which has the Philadelphia chromosome.[2] It may be used both in initial cases of chronic phase CML as well as in accelerated and chronic phase CML that has not responded to imatinib.[2][1] It is taken by mouth.[1]

Common side effects may include low platelets, low white blood cells, anemia, rashes, vomiting, diarrhea, and joint pains.[1] Other serious side effects may include QT prolongation, sudden death, pancreatitis, and liver problems.[1] It is not safe for use during pregnancy.[1] Nilotinib is a Bcr-Abl tyrosine kinase inhibitor and works by interfering with signalling within the cancer cell.[1]

Nilotinib was approved for medical use in the United States in 2007.[1] It is on the World Health Organization's List of Essential Medicines.[5] In the United Kingdom it costs the NHS £2,433 per month as of 2018.[6] In the United States this amount costs US$14,368 as of 2019.[7]

Medical uses[edit | edit source]

It is used to treat Philadelphia chromosome (Ph+)-positive chronic myelogenous leukaemia.[4]

Dosage[edit | edit source]

The defined daily dose is not established.[3]

Side effects[edit | edit source]

See also: List of adverse effects of nilotinib

Nilotinib has a number of side effects including headache, fatigue, gastrointestinal problems such as nausea, vomiting, diarrhea and constipation, muscle and joint pain, rash and other skin conditions, flu-like symptoms, and reduced blood cell count. Less typical side effects are those of the cardiovascular system, such as high blood pressure, various types of arrhythmia, and prolonged QT interval. Nilotinib can also affect the body's electrolyte and glucose balance.[8] Though lung-related adverse effects are rare when compared with imatinib and dasatinib, there is a case report of acute respiratory failure from diffuse alveolar hemorrhage in a people taking nilotinib.[9]

Nilotinib carries a black box warning in the United States for possible heart complications.[10][11] Contraindications include long QT syndrome, hypokalaemia, hypomagnesaemia, pregnancy, planned pregnancy, lactation and galactose/lactose intolerance.[4][12]

Cautions include:[4]

  • Myelosuppression
  • Tumour lysis syndrome
  • Liver impairment
  • History of pancreatitis
  • Check serum lipase periodically in order to detect pancreatitis
  • Total gastrectomy
  • Avoid pregnancy or impregnating women

Dose reduction has been recommended in people with liver problems which involves recommendation of lower starting dose and monitoring of any hepatic function abnormalities.[13]

Hepatitis B virus reactivation may also occur.[6]

Interactions[edit | edit source]

Nilotinib has been reported as a substrate for OATP1B1 and OATP1B3. Interaction of nilotinib with OATP1B1 and OATP1B3 may alter its hepatic disposition and can lead to transporter mediated drug-drug interactions.[13] Nilotinib is an inhibitor of OATP-1B1 transporter but not for OATP-1B3.[14]

It is a substrate for CYP3A4 and hence grapefruit juice and other CYP3A4 inhibitors[15] will increase its action and inducers like St. John's wort[16] will decrease it. Patients report that pomegranates and starfruit may also interfere.

Food should not be eaten two hours before or one hour afterwards because it unpredictably increases its bioavailability, approximately doubling it.

Pharmacology[edit | edit source]

Crystal structure of Abl kinase domain (blue) in complex with nilotinib (red)

Nilotinib inhibits the kinases BCR-ABL,[17] KIT, LCK, EPHA3, EPHA8, DDR1, DDR2, PDGFRB, MAPK11 and ZAK.[18]

Structurally related to imatinib,[19] It is 10–30 fold more potent than imatinib in inhibiting Bcr-Abl tyrosine kinase activity and proliferation of Bcr-Abl expressing cells.[19][20][21][22]

History[edit | edit source]

See also: Discovery and development of Bcr-Abl tyrosine kinase inhibitors

Nilotinib was developed by Novartis.[1] It was developed based on the structure of the Abl-imatinib complex to address imatinib intolerance and resistance.[23][20][21]

It was approved for medical use by the FDA in October 2007,[8] EMA in September 2009,[24] MHRA in November 2007,[25] and TGA in January 2008.[12]

Society and culture[edit | edit source]

In the United Kingdom it costs the NHS £2,432.85 per month as of 2018.[6] In the United States this amount costs US$14,367.94 as of 2019.[7]

Research[edit | edit source]

Parkinson's disease[edit | edit source]

There is weak evidence that nilotinib may be beneficial with Parkinson's disease (PD), with a small clinical trial suggesting it might halt progression and improve symptoms.[26] However, there were significant side effects including infection, liver function tests abnormalities, hallucinations and heart attack, and the benefit in PD disappeared at follow up after drug discontinuation, raising question as to whether it was truly a disease modifying therapy. Nilotinib is currently undergoing phase II studies for treatment of Parkinson's.[27] Scientists and medical professionals have advised caution with over-optimistic interpretation of its effects in Parkinson's due to the significant media hype surrounding the small and early clinical trial.[28][29] Dystonia and cognitive impairment have also been reported as side effects.[30]

Other[edit | edit source]

Novartis announced on April 11, 2011 that it was discontinuing a phase III trial of nilotinib as the first-line treatment of gastrointestinal stromal tumor (GIST) based on the recommendation of an independent data monitoring committee. Interim results showed Tasigna is unlikely to demonstrate superiority compared to Novartis's Gleevec (imatinib)*, the current standard of care in this setting.[31]

Low dose nilotinib is also being investigated for use for and Alzheimer's disease, as well as for ALS, dementia and Huntington's disease.[32]

References[edit | edit source]

  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 1.9 "Nilotinib Monograph for Professionals". Drugs.com. Archived from the original on 14 July 2021. Retrieved 14 November 2019.
  2. ↑ 2.0 2.1 2.2 "Nilotinib". National Cancer Institute. 1 February 2008. Archived from the original on 14 July 2021. Retrieved 14 November 2019.
  3. ↑ 3.0 3.1 "WHOCC - ATC/DDD Index". www.whocc.no. Archived from the original on 25 November 2020. Retrieved 10 September 2020.
  4. ↑ 4.0 4.1 4.2 4.3 4.4 4.5 4.6 4.7 "Tasigna (nilotinib) dosing, indications, interactions, adverse effects, and more". Medscape Reference. WebMD. Archived from the original on 17 July 2021. Retrieved 25 January 2014.
  5. ↑ "World Health Organization model list of essential medicines: 21st list 2019". 2019. hdl:10665/325771. {{cite journal}}: Cite journal requires |journal= (help)
  6. ↑ 6.0 6.1 6.2 British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 960. ISBN 9780857113382.
  7. ↑ 7.0 7.1 "Tasigna Prices, Coupons & Patient Assistance Programs". Drugs.com. Archived from the original on 24 December 2019. Retrieved 14 November 2019.
  8. ↑ 8.0 8.1 "Complete Nilotinib information from Drugs.com". Drugs.com. Archived from the original on 1 February 2014. Retrieved 25 January 2014.
  9. ↑ Donatelli, Christopher; Chongnarungsin, Daych; Ashton, Rendell (2014). "Acute respiratory failure from nilotinib-associated diffuse alveolar hemorrhage". Leukemia & Lymphoma. 55 (10): 1–6. doi:10.3109/10428194.2014.887714. PMID 24467220.
  10. ↑ "FDA Approves Tasigna for Treatment of Philadelphia Chromosome Positive Chronic Myeloid Leukemia". U.S. Food and Drug Administration. 2007-10-30. Archived from the original on 2009-08-27. Retrieved 2009-08-04.
  11. ↑ "Prescribing information for Tasigna (nilotinib) Capsules" (PDF). NDA 022068. U.S. FDA. 2007-10-29. Archived (PDF) from the original on 2009-08-14. Retrieved 2009-08-04.
  12. ↑ 12.0 12.1 "TASIGNA® nilotinib" (PDF). TGA eBusiness Services. 21 October 2013. Archived from the original on 6 April 2017. Retrieved 25 January 2014.
  13. ↑ 13.0 13.1 Khurana V, Minocha M, Pal D, Mitra AK (March 2014). "Role of OATP-1B1 and/or OATP-1B3 in hepatic disposition of tyrosine kinase inhibitors". Drug Metabol Drug Interact. 29 (3): 179–90. doi:10.1515/dmdi-2013-0062. PMC 4407685. PMID 24643910.
  14. ↑ Khurana V, Minocha M, Pal D, Mitra AK (May 2014). "Inhibition of OATP-1B1 and OATP-1B3 by tyrosine kinase inhibitors". Drug Metabol Drug Interact. 29 (4): 249–59. doi:10.1515/dmdi-2014-0014. PMC 4407688. PMID 24807167.
  15. ↑ Bailey, David G; Malcolm, J; Arnold, O; David Spence, J (1998-08-01). "Grapefruit juice–drug interactions". British Journal of Clinical Pharmacology. 46 (2): 101–110. doi:10.1046/j.1365-2125.1998.00764.x. ISSN 0306-5251. PMC 1873672. PMID 9723817.
  16. ↑ Komoroski, Bernard J.; Zhang, Shimin; Cai, Hongbo; Hutzler, J. Matthew; Frye, Reginald; Tracy, Timothy S.; Strom, Stephen C.; Lehmann, Thomas; Ang, Catharina Y. W. (2004-05-01). "Induction and inhibition of cytochromes P450 by the St. John's wort constituent hyperforin in human hepatocyte cultures". Drug Metabolism and Disposition. 32 (5): 512–518. doi:10.1124/dmd.32.5.512. ISSN 0090-9556. PMID 15100173.
  17. ↑ Weisberg E, Manley P, Mestan J, Cowan-Jacob S, Ray A, Griffin JD (June 2006). "AMN107 (nilotinib): a novel and selective inhibitor of BCR-ABL". Br. J. Cancer. 94 (12): 1765–9. doi:10.1038/sj.bjc.6603170. PMC 2361347. PMID 16721371.
  18. ↑ Manley, PW; Drueckes, P; Fendrich, G; Furet, P; Liebetanz, J; Martiny-Baron, G; Mestan, J; Trappe, J; et al. (2010). "Extended kinase profile and properties of the protein kinase inhibitor nilotinib". Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1804 (3): 445–53. doi:10.1016/j.bbapap.2009.11.008. PMID 19922818.
  19. ↑ 19.0 19.1 Manley, P.; Cowan-Jacob, S.; Mestan, J. (2005). "Advances in the structural biology, design and clinical development of Bcr-Abl kinase inhibitors for the treatment of chronic myeloid leukaemia". Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1754 (1–2): 3–13. doi:10.1016/j.bbapap.2005.07.040. PMID 16172030.
  20. ↑ 20.0 20.1 Jabbour, E.; Cortes, J.; Kantarjian, H. (2009). "Nilotinib for the treatment of chronic myeloid leukemia: An evidence-based review". Core Evidence. 4: 207–213. doi:10.2147/CE.S6003. PMC 2899790. PMID 20694077.
  21. ↑ 21.0 21.1 Olivieri, A.; Manzione, L. (2007). "Dasatinib: a new step in molecular target therapy". Annals of Oncology. 18 Suppl 6: vi42–vi46. doi:10.1093/annonc/mdm223. PMID 17591830.
  22. ↑ Breccia, M.; Alimena, G. (2010). "Nilotinib: a second-generation tyrosine kinase inhibitor for chronic myeloid leukemia". Leukemia Research. 34 (2): 129–134. doi:10.1016/j.leukres.2009.08.031. PMID 19783301.
  23. ↑ Manley, P.; Stiefl, N.; Cowan-Jacob, S.; Kaufman, S.; Mestan, J.; Wartmann, M.; Wiesmann, M.; Woodman, R.; Gallagher, N. (2010). "Structural resemblances and comparisons of the relative pharmacological properties of imatinib and nilotinib". Bioorganic & Medicinal Chemistry. 18 (19): 6977–6986. doi:10.1016/j.bmc.2010.08.026. PMID 20817538.
  24. ↑ "Tasigna : EPAR - Product Information" (PDF). European Medicines Agency. Novartis Europharm Ltd. 18 October 2013. Archived (PDF) from the original on 4 February 2014. Retrieved 25 January 2014.
  25. ↑ "Tasigna 150mg Hard Capsules - Summary of Product Characteristics (SPC)". electronic Medicines Compendium. Novartis Pharmaceuticals UK Ltd. 9 September 2013. Archived from the original on 1 February 2014. Retrieved 25 January 2014.
  26. ↑ Pagan, F.; Hebron, M.; Valadez, E. H.; Torres-Yaghi, Y.; Huang, X.; Mills, R. R.; Wilmarth, B. M.; Howard, H.; Dunn, C.; Carlson, A.; Lawler, A.; Rogers, S. L.; Falconer, R. A.; Ahn, J.; Li, Z.; Moussa, C. (2016). "Nilotinib Effects in Parkinson's disease and Dementia with Lewy bodies". Journal of Parkinson's Disease. 6 (3): 503–17. doi:10.3233/JPD-160867. PMC 5008228. PMID 27434297.
  27. ↑ Dash, Deepa (2019). "Anticancer Drugs for Parkinson's Disease: Is It a Ray of Hope or Only Hype?". Annals of Indian Academy of Neurology. 22 (1): 13–16. doi:10.4103/aian.AIAN_177_18. PMC 6327695. PMID 30692753.
  28. ↑ Robledo, I.; Jankovic, J. (2017). "Media hype: Patient and scientific perspectives on misleading medical news". Movement Disorders. 32 (9): 1319–1323. doi:10.1002/mds.26993. PMID 28370445.
  29. ↑ Wyse, R. K.; Brundin, P.; Sherer, T. B. (2016). "Nilotinib - Differentiating the Hope from the Hype". Journal of Parkinson's Disease. 6 (3): 519–22. doi:10.3233/JPD-160904. PMC 5044778. PMID 27434298.
  30. ↑ Dash, D; Goyal, V (2019). "Anticancer Drugs for Parkinson's Disease: Is It a Ray of Hope or Only Hype?". Annals of Indian Academy of Neurology. 22 (1): 13–16. doi:10.4103/aian.AIAN_177_18. PMID 30692753.
  31. ↑ "Global Novartis News Archive". Archived from the original on 2014-02-22. Retrieved 2014-02-18.
  32. ↑ "Cancer drug prevents build-up of toxic brain protein". MedicalXpress.com. 10 May 2013. Archived from the original on 11 April 2017. Retrieved 11 April 2017.

External links[edit | edit source]

External sites:
Identifiers:

Categories: [Orphan drugs] [Non-receptor tyrosine kinase inhibitors] [Imidazoles] [Novartis brands] [Trifluoromethyl compounds] [Benzanilides] [Aminopyrimidines] [Pyridines] [RTT] [World Health Organization essential medicines]

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