dasatinib

{{Short description|Chemical compound}}

{{Use dmy dates|date=May 2025}}

{{cs1 config |name-list-style=vanc|display-authors=6}}

{{Drugbox

| Verifiedfields = changed

| verifiedrevid = 458266659

| IUPAC_name = N-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-
1-piperazinyl]-2-methyl-4-pyrimidinyl]amino]-5-thiazole
carboxamide monohydrate

| image = Dasatinib.svg

| image_class = skin-invert-image

| width = 325

| alt =

| image2 = Dasatinib-2GQG-ball-and-stick-flip.png

| width2 = 350

| alt2 =

| tradename = Sprycel, Dasanix

| Drugs.com = {{drugs.com|monograph|dasatinib}}

| MedlinePlus = a607063

| licence_EU = yes

| DailyMedID = Dasatinib

| licence_US = Dasatinib

| pregnancy_AU = D

| routes_of_administration = By mouth (tablets)

| ATC_prefix = L01

| ATC_suffix = EA02

| legal_AU = S4

| legal_AU_comment = {{cite web | title=Sprycel (Dasatinib) | website=Therapeutic Goods Administration (TGA) | url=https://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent&id=CP-2010-PI-02657-3 | format=PDF | access-date=18 July 2020}}

| legal_UK = POM

| legal_US = Rx-only

| legal_EU = Rx-only

| legal_EU_comment =

| legal_status = Rx-only

| bioavailability =

| protein_bound = 96%

| metabolism = Liver

| elimination_half-life = 1.3 to 5 hours

| excretion = Fecal (85%), kidney (4%)

| IUPHAR_ligand = 5678

| CAS_number_Ref = {{cascite|correct|CAS}}

| CAS_number = 302962-49-8

| PubChem = 3062316

| DrugBank_Ref = {{drugbankcite|correct|drugbank}}

| DrugBank = DB01254

| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}

| ChemSpiderID = 2323020

| UNII_Ref = {{fdacite|changed|FDA}}

| UNII = X78UG0A0RN

| KEGG_Ref = {{keggcite|changed|kegg}}

| KEGG = D03658

| ChEBI_Ref = {{ebicite|correct|EBI}}

| ChEBI = 49375

| ChEMBL_Ref = {{ebicite|correct|EBI}}

| ChEMBL = 1421

| C=22 | H=26 | Cl=1 | N=7 | O=2 | S=1

| smiles = Cc1cccc(c1NC(=O)c2cnc(s2)Nc3cc(nc(n3)C)N4CCN(CC4)CCO)Cl

| StdInChI_Ref = {{stdinchicite|correct|chemspider}}

| StdInChI = 1S/C22H26ClN7O2S/c1-14-4-3-5-16(23)20(14)28-21(32)17-13-24-22(33-17)27-18-12-19(26-15(2)25-18)30-8-6-29(7-9-30)10-11-31/h3-5,12-13,31H,6-11H2,1-2H3,(H,28,32)(H,24,25,26,27)

| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}

| StdInChIKey = ZBNZXTGUTAYRHI-UHFFFAOYSA-N

}}

Dasatinib, sold under the brand name Sprycel among others, is a targeted therapy medication used to treat certain cases of chronic myelogenous leukemia (CML) and acute lymphoblastic leukemia (ALL).{{cite web|title=Dasatinib|url=https://www.drugs.com/monograph/dasatinib.html|publisher=The American Society of Health-System Pharmacists|access-date= 8 December 2017}} Specifically it is used to treat cases that are Philadelphia chromosome-positive (Ph+). It is taken by mouth.

Common adverse effects include low white blood cells, low blood platelets, anemia, swelling, rash, and diarrhea. Severe adverse effects may include bleeding, pulmonary edema, heart failure, and prolonged QT syndrome. Use during pregnancy may result in harm to the fetus. It is a tyrosine-kinase inhibitor and works by blocking a number of tyrosine kinases such as Bcr-Abl and the Src kinase family.

Dasatinib was approved for medical use in the United States and in the European Union in 2006.{{cite web | title=Sprycel EPAR | website=European Medicines Agency (EMA) | date=17 September 2018 | url=https://www.ema.europa.eu/en/medicines/human/EPAR/sprycel | access-date=28 April 2020}} {{PD-notice}} It is on the World Health Organization's List of Essential Medicines.{{cite book | vauthors = ((World Health Organization)) | title = World Health Organization model list of essential medicines: 21st list 2019 | year = 2019 | hdl = 10665/325771 | author-link = World Health Organization | publisher = World Health Organization | location = Geneva | id = WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO | hdl-access=free }}

Medical uses

Dasatinib is used to treat people with chronic myeloid leukemia and people with acute lymphoblastic leukemia who are positive for the Philadelphia chromosome.{{cite journal | vauthors = Keating GM | title = Dasatinib: A Review in Chronic Myeloid Leukaemia and Ph+ Acute Lymphoblastic Leukaemia | journal = Drugs | volume = 77 | issue = 1 | pages = 85–96 | date = January 2017 | pmid = 28032244 | doi = 10.1007/s40265-016-0677-x | s2cid = 207489056 }}

In the EU dasatinib is indicated for children with

  • newly diagnosed Philadelphia chromosome-positive chronic myelogenous leukaemia in chronic phase (Ph+ CML CP) or Ph+ CML CP resistant or intolerant to prior therapy including imatinib.
  • newly diagnosed Ph+ acute lymphoblastic leukaemia (ALL) in combination with chemotherapy.
  • newly diagnosed Ph+ CML in chronic phase (Ph+ CML-CP) or Ph+ CML-CP resistant or intolerant to prior therapy including imatinib.

and adults with

  • newly diagnosed Philadelphia-chromosome-positive (Ph+) chronic myelogenous leukaemia (CML) in the chronic phase;
  • chronic, accelerated or blast phase CML with resistance or intolerance to prior therapy including imatinib mesilate;
  • Ph+ acute lymphoblastic leukaemia (ALL) and lymphoid blast CML with resistance or intolerance to prior therapy.

Adverse effects

The most common side effects are infection, suppression of the bone marrow (decreasing numbers of leukocytes, erythrocytes, and thrombocytes),{{cite journal | vauthors = Olivieri A, Manzione L | title = Dasatinib: a new step in molecular target therapy | journal = Annals of Oncology | volume = 18 | issue = Suppl 6 | pages = vi42–vi46 | date = June 2007 | pmid = 17591830 | doi = 10.1093/annonc/mdm223 | doi-access = free }} headache, hemorrhage (bleeding), pleural effusion (fluid around the lungs), dyspnea (difficulty breathing), diarrhea, vomiting, nausea (feeling sick), abdominal pain (belly ache), skin rash, musculoskeletal pain, tiredness, swelling in the legs and arms and in the face, fever. Neutropenia and myelosuppression were common toxic effects. Fifteen people (of 84, i.e. 18%) in the above-mentioned study developed pleural effusions, which was a suspected side effect of dasatinib. Some of these people required thoracentesis or pleurodesis to treat the effusions. Other adverse events included mild to moderate diarrhea, peripheral edema, and headache. A small number of people developed abnormal liver function tests which returned to normal without dose adjustments. Mild hypocalcemia was also noted, but did not appear to cause any significant problems. Several cases of pulmonary arterial hypertension (PAH) were found in people treated with dasatinib,{{cite web|url=http://www.nelm.nhs.uk/en/NeLM-Area/News/2011---August/16/Healthcare-professional-communication-regarding-association-of-dasatinib-Sprycel-with-pulmonary-arterial-hypertension/|title=NHS - Healthcare News|website=nelm.nhs.uk|access-date=27 September 2011|archive-url=https://archive.today/20130505141147/http://www.nelm.nhs.uk/en/NeLM-Area/News/2011---August/16/Healthcare-professional-communication-regarding-association-of-dasatinib-Sprycel-with-pulmonary-arterial-hypertension/|archive-date=5 May 2013|url-status=dead}} possibly due to pulmonary endothelial cell damage.{{cite journal | vauthors=Yurttaş NO, Eşkazan AE | title=Dasatinib-induced pulmonary arterial hypertension | journal=British Journal of Clinical Pharmacology | volume=84 | issue=5 | pages=835–845 | year=2018 | pmc =5903230 |doi = 10.1111/bcp.13508 | pmid=29334406}}

On 11 October 2011, the U.S. Food and Drug Administration (FDA) announced that dasatinib may increase the risk of a rare but serious condition in which there is abnormally high blood pressure in the arteries of the lungs (pulmonary hypertension, PAH).{{cite web | title=Sprycel (dasatinib) and risk of pulmonary arterial hypertension | website=U.S. Food and Drug Administration (FDA) | date=23 September 2011 | url=https://www.fda.gov/drugs/drug-safety-and-availability/fda-drug-safety-communication-sprycel-dasatinib-and-risk-pulmonary-arterial-hypertension | archive-url=https://web.archive.org/web/20190819185811/https://www.fda.gov/drugs/drug-safety-and-availability/fda-drug-safety-communication-sprycel-dasatinib-and-risk-pulmonary-arterial-hypertension | url-status=dead | archive-date=19 August 2019 | access-date=28 April 2020}} {{PD-notice}} Symptoms of PAH may include shortness of breath, fatigue, and swelling of the body (such as the ankles and legs). In reported cases, people developed PAH after starting dasatinib, including after more than one year of treatment. Information about the risk was added to the Warnings and Precautions section of the Sprycel drug label. In studies between 2009 and 2017 dasatinib-induced PAH was initiated between 0.3 and 74 months of daily drug usage at doses from 70 to 140 mg.{{cite journal | vauthors = Özgür Yurttaş N, Eşkazan AE | title = Dasatinib-induced pulmonary arterial hypertension | journal = British Journal of Clinical Pharmacology | volume = 84 | issue = 5 | pages = 835–845 | date = May 2018 | pmid = 29334406 | pmc = 5903230 | doi = 10.1111/bcp.13508 | publisher = Wiley }} Reported dasatinib-induced PAH had improvements after cessation of drug treatment.

Pharmacology

File:2GQG Abl1Kinase Dasatinib.png (blue) in complex with dasatinib (red).]]

Dasatinib is an ATP-competitive protein tyrosine kinase inhibitor. The main targets of dasatinib are BCR/Abl (the "Philadelphia chromosome"), Src, c-Kit, ephrin receptors, and several other tyrosine kinases.{{cite journal | vauthors=Piscitani L, Sirolli V, Morroni M, Bonomini M | title=Nephrotoxicity Associated with Novel Anticancer Agents (Aflibercept, Dasatinib, Nivolumab): Case Series and Nephrological Considerations | journal= International Journal of Molecular Sciences| volume=21 | issue=14 | pages=e4878 | year=2020 | doi = 10.3390/ijms21144878 | pmid=32664269| pmc=7402330 | doi-access=free }} Strong inhibition of the activated BCR-ABL kinase distinguishes dasatinib from other CML treatments, such as imatinib and nilotinib.{{cite journal | vauthors=Braun TP, Eide CA, Druker BJ| title=Response and Resistance to BCR-ABL1-Targeted Therapies | journal= Cancer Cell| volume=37 | issue=4 | pages=530–542| year=2020 | doi = 10.1016/j.ccell.2020.03.006 | pmid=32289275| pmc=7722523 }} Although dasatinib only has a plasma half-life of three to five hours, the strong binding to BCR-ABL1 results in a longer duration of action.

History

{{see also|Discovery and development of Bcr-Abl tyrosine kinase inhibitors}}

Dasatinib was developed by collaboration of Bristol-Myers Squibb and Otsuka Pharmaceutical Co., Ltd,{{cite web | title = Otsuka and Bristol-Myers Squibb Announce a Change in Contract Regarding Collaboration in Japan in the Oncology Therapy Area | date = 17 April 2023| url = https://www.otsuka.co.jp/en/company/release/2015/0302_01.html}}{{cite press release | title = FDA Approves U.S. Product Labeling Update for Sprycel (dasatinib) to Include Three-Year First-Line and Five-Year Second-Line Efficacy and Safety Data in Chronic Myeloid Leukemia in Chronic Phase | url = https://news.bms.com/news/r-and-d/2013/FDA-Approves-US-Product-Labeling-Update-for-Sprycel-dasatinib-to-Include-Three-Year-First-Line-and-Five-Year-Second-Line-Efficacy-and-Safety-Data-in-Chronic-Myeloid-Leukemia-in-Chronic-Phase/default.aspx| work = Bristol-Myers Squibb | access-date = 23 April 2015 | archive-date = 20 September 2018 | archive-url = https://web.archive.org/web/20180920151146/https://news.bms.com/press-release/rd-news/fda-approves-us-product-labeling-update-sprycel-dasatinib-include-three-year-f | url-status = dead }}{{cite press release | title = Bristol-Myers Squibb Announces Extension of U.S. Agreement for ABILIFY and Establishment of an Oncology Collaboration with Otsuka | url = https://news.bms.com/news/corporate-financial/2009/Bristol-Myers-Squibb-Announces-Extension-of-US-Agreement-for-ABILIFY-and-Establishment-of-an-Oncology-Collaboration-with-Otsuka/default.aspx| archive-url = https://web.archive.org/web/20150131004436/http://news.bms.com/press-release/financial-news/bristol-myers-squibb-announces-extension-us-agreement-abilify-and-estab | url-status = dead | archive-date = 31 January 2015 | work = Bristol-Myers Squibb }} and named for Bristol-Myers Squibb research fellow Jagabandhu Das, whose program leader says that the drug would not have come into existence had he not challenged some of the medicinal chemists' underlying assumptions at a time when progress in the development of the molecule had stalled.{{cite web |vauthors=Drahl C |title=How Jagabandhu Das made dasatinib possible |url=http://cenblog.org/the-haystack/2012/01/jagabandhu-das-dasatinib/ |website=The Safety Zone blog |publisher=Chemical & Engineering News |access-date=29 August 2016 |date=16 January 2012 |archive-date=10 December 2017 |archive-url=https://web.archive.org/web/20171210232159/http://cenblog.org/the-haystack/2012/01/jagabandhu-das-dasatinib/ |url-status=dead }}

Society and culture

= Legal status =

Dasatinib was approved for use in the United States in June 2006 and in the European Union in November 2006{{cite web | title=Drug Approval Package: Sprycel (Dasatinib) NDA #021986 & 022072 | website=U.S. Food and Drug Administration (FDA) | date=6 September 2006 | url=https://www.accessdata.fda.gov/drugsatfda_docs/nda/2006/021986_022072_SprycelTOC.cfm | archive-url=https://web.archive.org/web/20200919231024/https://www.accessdata.fda.gov/drugsatfda_docs/nda/2006/021986_022072_SprycelTOC.cfm | url-status=dead | archive-date=19 September 2020 | access-date=28 April 2020}}

In October 2010, dasatinib was approved in the United States for the treatment of newly diagnosed adults with Philadelphia chromosome positive chronic myeloid leukemia in chronic phase (CP-CML).{{cite web | title=2010 Notifications | website=U.S. Food and Drug Administration (FDA) | date=18 November 2010 | url=https://www.fda.gov/drugs/resources-information-approved-drugs/2010-notifications | archive-url=https://web.archive.org/web/20200428151523/https://www.fda.gov/drugs/resources-information-approved-drugs/2010-notifications | url-status=dead | archive-date=28 April 2020 | access-date=28 April 2020}} {{PD-notice}}

In November 2017, dasatinib was approved in the United States for the treatment of children with Philadelphia chromosome-positive (Ph+) chronic myeloid leukemia (CML) in the chronic phase.{{cite web | title=FDA approves dasatinib for pediatric patients with CML | website=U.S. Food and Drug Administration (FDA) | date=9 November 2017 | url=https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-dasatinib-pediatric-patients-cml | archive-url=https://web.archive.org/web/20190612185253/https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-dasatinib-pediatric-patients-cml | url-status=dead | archive-date=12 June 2019 | access-date=28 April 2020}} {{PD-notice}}

Approval was based on data from 97 pediatric participants with chronic phase CML evaluated in two trials—a Phase I, open-label, non-randomized, dose-ranging trial and a Phase II, open-label, non-randomized trial. Fifty-one participants exclusively from the Phase II trial were newly diagnosed with chronic phase CML and 46 participants (17 from the Phase I trial and 29 from the Phase II trial) were resistant or intolerant to previous treatment with imatinib. The majority of participants were treated with dasatinib tablets 60 mg/m2 body surface area once daily. Participants were treated until disease progression or unacceptable toxicity.

=Economics=

The Union for Affordable Cancer Treatment objected to the price of dasatinib, in a letter to the U.S. trade representative. The average wholesale price in the U.S. is $367 per day, twice the price in other high income countries. The price in India, where the average annual per capita income is $1,570, and where most people pay out of pocket, is Rs6627 ($108) a day. Indian manufacturers offered to supply generic versions for $4 a day, but, under pressure from the U.S., the Indian Department of Industrial Policy and Promotion refused to issue a compulsory license.{{cite journal | vauthors = Cohen D | title = US trade rep is pressing Indian government to forbid production of generic cancer drug, consortium says | journal = BMJ | volume = 349 | pages = g6593 | date = November 2014 | pmid = 25370846 | doi = 10.1136/bmj.g6593 | s2cid = 206903723 }}

Bristol-Myers Squibb justified the high prices of cancer drugs with the high R&D costs, but the Union of Affordable Cancer Treatment said that most of the R&D costs came from the U.S. government, including National Institutes of Health funded research and clinical trials, and a 50% tax credit. In England and Wales, the National Institute for Health and Care Excellence recommended against dasatinib because of the high cost-benefit ratio.

The Union for Affordable Cancer Treatment said that "the dasatinib dispute illustrates the shortcomings of US trade policy and its impact on cancer patients"

=Brand names=

In Bangladesh dasatinib is available under the trade name Dasanix by Beacon Pharmaceuticals.{{Cite web |title=Dasanix |url=https://medex.com.bd/brands/27272/dasanix-50mg |publisher=Medex |access-date=19 May 2021}} In India, It is marketed under the brand name Nextki by Emcure Pharmaceuticals.{{medcn|date=April 2020}}

Research

Dasatinib has been shown to eliminate senescent cells in cultured adipocyte progenitor cells.

=Dasatinib+Quercetin=

Dasatinib has been shown to induce apoptosis in senescent cells by inhibiting Src kinase, whereas quercetin inhibits the anti-apoptotic protein Bcl-xL.{{cite journal | vauthors=Kirkland JL, Tchkonia T | title=Senolytic drugs: from discovery to translation | journal=Journal of Internal Medicine | year=2020 | volume=288 | issue=5 | pages=518–536 | doi = 10.1111/joim.13141 | pmc=7405395 | pmid=32686219}} Administration of dasatinib along with quercetin to mice improved cardiovascular function and eliminated senescent cells.{{cite journal | vauthors=Paez-Ribes M, González-Gualda E, Doherty GJ, Muñoz-Espín D | title=Targeting senescent cells in translational medicine | journal=EMBO Molecular Medicine | volume=11 | issue=12 | pages=e10234 | year=2019 | doi = 10.15252/emmm.201810234 | pmc=6895604 | pmid=31746100}} Aged mice given dasatinib with quercetin showed improved health and survival.

A study of fourteen human patients with idiopathic pulmonary fibrosis (a disease characterized by increased numbers of senescent cells) given dasatinib and quercetin showed improved physical function and evidence of reduced senescent cells.

References

{{reflist}}

Further reading

{{refbegin}}

  • {{cite journal | vauthors = Lombardo LJ, Lee FY, Chen P, Norris D, Barrish JC, Behnia K, Castaneda S, Cornelius LA, Das J, Doweyko AM, Fairchild C, Hunt JT, Inigo I, Johnston K, Kamath A, Kan D, Klei H, Marathe P, Pang S, Peterson R, Pitt S, Schieven GL, Schmidt RJ, Tokarski J, Wen ML, Wityak J, Borzilleri RM | display-authors = 6 | title = Discovery of N-(2-chloro-6-methyl- phenyl)-2-(6-(4-(2-hydroxyethyl)- piperazin-1-yl)-2-methylpyrimidin-4- ylamino)thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays | journal = Journal of Medicinal Chemistry | volume = 47 | issue = 27 | pages = 6658–61 | date = December 2004 | pmid = 15615512 | doi = 10.1021/jm049486a }}

{{refend}}

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