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F r o m W i k i p e d i a , t h e f r e e e n c y c l o p e d i a
Tepadina
Monograph
a682821
Intravenous , intracavitary, intravesical
UK : POM (Prescription only)
US : WARNING [1] Rx-only[4]
EU : Rx-only[5]
Liver (CYP2B6 , CYP3A )
1.5–4.1 hours
Kidney 6 hours for thiotepa 8 hours for TEPA
1,1′ ,1′ ′ -Phosphorothioyltriaziridine
100.000.124
Chemical and physical data
C 6 H 12 N 3 P S
189.22 g·mol−1
InChI=1S/C6H12N3PS/c11-10(7-1-2-7,8-3-4-8)9-5-6-9/h1-6H2 Y
Key:FOCVUCIESVLUNU-UHFFFAOYSA-N Y
Thiotepa (INN [6] ), sold under the brand name Tepadina , is a medication used to treat cancer .[4] [5] [7]
Thiotepa is an organophosphorus compound with the formula (C 2 H 4 N )3 PS.[8] It is an analog of N ,N ′ ,N ″ -triethylenephosphoramide (TEPA ), which contains tetrahedral phosphorus and is structurally akin to phosphate . It is manufactured by heating aziridine with thiophosphoryl chloride .[citation needed ]
Medical uses [ edit ]
Thiotepa is indicated for use in combination with other chemotherapy agents to treat cancer.[4] [5] [7] This can be with or without total body irradiation (TBI), as a conditioning treatment prior to allogeneic or autologous hematopoietic progenitor cell transplantation (HPCT) in hematological diseases in adults and children.[5] [7] These diseases include Hodgkin's disease and leukaemia.[7] Thiotepa is also used with high-dose chemotherapy with HPCT support to treat certain solid tumors in adult and children.[5] [7]
Thiotepa is used in the palliation of many neoplastic diseases . The best results are found in the treatment of adenocarcinoma of the breast , adenocarcinoma of the ovary , papillary thyroid cancer and bladder cancer . Thiotepa is used to control intracavitary effusions caused by serosal neoplastic deposits.[7]
Intravesical use [ edit ]
Thiotepa is used as intravesical chemotherapy in bladder cancer.[9]
It may be used prophylactically to prevent seeding of tumor cells at cystoscopic biopsy; as an adjunctive agent at the time of biopsy; or as a therapeutic agent to prevent recurrence after cystoscopic resection of bladder tumor (transurethral resection of bladder tumor , TURBT).[medical citation needed ] Efficacy in tumor control may reach 55%.[medical citation needed ] The main toxicity of this therapy is bone marrow suppression due to systemic absorption of the drug.[medical citation needed ]
Side effects [ edit ]
The main side effect of thiotepa is bone marrow suppression resulting in leukopenia , thrombocytopenia and anemia .[10] Liver and lung toxicity may also occur.[medical citation needed ]
History [ edit ]
Thiotepa was developed by the American Cyanamid company in the early 1950s and reported to media outlets in 1953.[11] In 1959, thiotepa was registered with the Food and Drug Administration (FDA) as a drug therapy for several solid cancers.[12]
In January 2007, the European Medicines Agency (EMA) designated thiotepa as an orphan drug . In April 2007, the United States FDA designated thiotepa as a conditioning treatment for use prior to hematopoietic stem cell transplantation .[13]
In 2024 The (FDA) approved the New Drug Application (NDA) for Tepylute, a ready-to-dilute formulation of thiotepa to treat breast and ovarian cancer .[14] [15]
References [ edit ]
^ "Cancer therapies" . Health Canada . 8 May 2018. Retrieved 13 April 2024 .
^ a b c "Tepadina- thiotepa injection, powder, for solution" . DailyMed . Archived from the original on 12 August 2021. Retrieved 11 August 2021 .
^ a b c d e "Tepadina EPAR" . European Medicines Agency (EMA) . 17 September 2018. Archived from the original on 6 March 2021. Retrieved 30 April 2021 .
^ "International Non-Proprietary Names for Pharmaceutical Preparations. Recommended International Non-Proprietary Names (Rec. I.N.N.): List 4" (PDF) . World Health Organization. March 1962. p. 111. Archived from the original (PDF) on 18 May 2016. Retrieved 27 November 2016 .
^ a b c d e f "Urgent, Thiotepa update" (PDF) . U.S. Food and Drug Administration (FDA). 5 April 2011. Archived (PDF) from the original on 9 November 2011. Retrieved 25 November 2011 .
^ Maanen MJ, Smeets CJ, Beijnen JH (August 2000). "Chemistry, pharmacology and pharmacokinetics of N,N',N" -triethylenethiophosphoramide (ThioTEPA)". Cancer Treatment Reviews . 26 (4 ): 257–68. doi :10.1053/ctrv.2000.0170 . PMID 10913381 .
^ Droller M (2004). Urothelial Tumors . PMPH-USA. p. 207. ISBN 978-1-55009-173-1 . Archived from the original on 11 January 2023. Retrieved 16 September 2017 .
^ Agnelli G, de Cunto M, Gresele P, del Favero A (June 1982). "Early onset life-threatening myelosuppression after low dose of intravesical thiotepa" . Postgraduate Medical Journal . 58 (680): 380–1. doi :10.1136/pgmj.58.680.380 . PMC 2426344 . PMID 6812036 .
^ Sykes MP, Karnofsky DA, Philips FS, Burchenal JH (1953). "Clinical studies on triethylenephosphoramide and diethylenephosphoramide, compounds with nitrogen-mustard-like activity" . Cancer . 6 (1 ): 142–148. doi :10.1002/1097-0142(195301)6:1<142::AID-CNCR2820060114>3.0.CO;2-W .
^ Kim KM, Roh JK, Wee H, Kim C (2016). Cancer Drug Discovery: Science and History . Springer. p. 82. ISBN 978-94-024-0844-7 .
^ "EMA Grants Adienne Marketing Rights for Tepadina" . Drug Discovery & Development. 19 March 2010. Retrieved 25 November 2011 .
^ "Shorla Oncology Announces FDA Approval for TEPYLUTE, A Novel Formulation to Treat Breast and Ovarian Cancer" .
^ "FDA Approves Tepylute in Breast and Ovarian Cancer" . Targeted Oncology . 28 June 2024. Retrieved 29 June 2024 .
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R e t r i e v e d f r o m " https://en.wikipedia.org/w/index.php?title=Thiotepa&oldid=1231942005 "
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