Denileukin diftitox|
| Trade names | Ontak, others |
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| AHFS/Drugs.com | Monograph |
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| MedlinePlus | a611024 |
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| License data |
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Routes of administration | Intravenous |
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| Drug class | Antineoplastic |
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| Elimination half-life | 70-80 min |
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Diphtheria toxin-Interleukin-2 fusion protein
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| Formula | C2560H4042N678O799S17 |
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| Molar mass | 57647.46 g·mol−1 |
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N Y (what is this?) (verify) |
Denileukin diftitox, sold under the brand name Ontak among others, is an anti-cancer medication used for the treatment of adults with T-cell lymphoma. It is an IL2-receptor-directed cytotoxin. It is an engineered protein combining interleukin-2 and diphtheria toxin.[3]
Medical uses
Denileukin diftitox is indicated for the treatment of adults with relapsed or refractory stage I-III cutaneous T-cell lymphoma after at least one prior systemic therapy.[1][2]
Adverse effects
The prescription label contains a boxed warning that capillary leak syndrome (CLS), including life-threatening or fatal reactions, can occur in people receiving denileukin diftitox.[1][2]
Society and culture
Legal status
In 1999, denileukin diftitox was approved by the US Food and Drug Administration (FDA) for the treatment of cutaneous T-cell lymphoma.[1][4]
References
External links
Targeted cancer therapy / antineoplastic agents (L01) |
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| CI monoclonal antibodies ("-mab") | | Receptor tyrosine kinase |
- ErbB: HER1/EGFR (Cetuximab
- Panitumumab)
- HER2/neu (Pertuzumab
- Trastuzumab (+hyaluronidase)
- Trastuzumab emtansine
- Trastuzumab deruxtecan
- Zanidatamab )
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| Others for solid tumors |
- EpCAM (Catumaxomab
- Edrecolomab)
- VEGF-A (Bevacizumab)
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| Leukemia/lymphoma |
- myeloid: CD33 (Gemtuzumab ozogamicin)
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| Other |
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- Tremelimumab
- Zenocutuzumab
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| Tyrosine kinase inhibitors ("-nib") | | Receptor tyrosine kinase |
- ErbB: HER1/EGFR (Afatinib
- Aumolertinib
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- Dacomitinib
- Erlotinib
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- Icotinib
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- BRAF
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- RTK class III: C-kit and PDGFR (Avapritinib
- Axitinib
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- Ripretinib
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- Toceranib)
- FLT3 (Lestaurtinib, Gilteritinib (AXL, ALK, LTK))
- VEGFR
- Axitinib
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- Vandetanib
- ALK
- Alectinib
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- Ceritinib
- Crizotinib
- Ensartinib
- Lorlatinib
- RET inhibitors: Entrectinib (ALK, ROS1, NTRK), Futibatinib (FGFR2), Infigratinib, Larotrectinib (NTRK), Pemigatinib (FGFR), Pralsetinib, Repotrectinib (ROS1, TRK, ALK), Selpercatinib (VEGFR, FGFR), Taletrectinib (ROS1), Vandetanib (VEGFR, EGFR).
- c-MET inhibitors: Cabozantinib (VEGFR), Capmatinib, Crizotinib (ALK)
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| Non-receptor |
- Janus kinase (JAK)
- Baricitinib
- Fedratinib
- Filgotinib
- Lestaurtinib
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- MAP2K (MEK)
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- Acalabrutinib
- Ibrutinib
- Orelabrutinib
- Pirtobrutinib
- Rilzabrutinib
- Zanubrutinib
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| Other |
- fusion protein against VEGF (Aflibercept)
- proapoptotic peptide against ANXA2 and prohibitin (Adipotide)
- hedgehog inhibitors
- Glasdegib
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- Tepotinib
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- Vandetanib
- Venetoclax
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Interleukin receptor modulators |
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| IL-1 |
- Agonists: Interleukin 1 (α, β)
- Mobenakin
- Pifonakin
- Antagonists: AF-12198
- Anakinra
- IL-1RA
- Isunakinra
- Antibodies: Canakinumab
- Gevokizumab
- Lutikizumab
- Decoy receptors: Rilonacept (IL-1 Trap)
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| IL-2 | |
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| IL-3 |
- Agonists: Daniplestim
- Interleukin 3
- Leridistim
- Milodistim
- Muplestim
- Promegapoietin
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| IL-4 |
- Agonists: Binetrakin
- Interleukin 4
- Interleukin 13
- Antibodies: Dupilumab
- Pascolizumab
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| IL-5 |
- Antibodies: Benralizumab
- Mepolizumab
- Reslizumab
- Antisense oligonucleotides: TPI ASM8
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| IL-6 |
- Agonists: Atexakin alfa
- Interleukin 6
- Antibodies: ARGX-109
- Clazakizumab
- Elsilimomab
- mAb 1339
- Olokizumab
- Sarilumab
- Siltuximab
- Sirukumab
- Tocilizumab
- Levilimab
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| IL-7 | |
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| IL-8 |
- See CXCR1 (IL-8Rα) and CXCR2 (IL-8Rβ) here instead.
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| IL-9 | |
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| IL-10 |
- Agonists: Ilodecakin
- Interleukin 10 (CSIF)
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| IL-11 | |
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| IL-12 |
- Agonists: Edodekin alfa
- Interleukin 12
- Antibodies: Briakinumab
- Ustekinumab
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| IL-13 |
- Agonists: Binetrakin
- Cintredekin besudotox
- Interleukin 4
- Interleukin 13
- Antibodies: Anrukinzumab
- Lebrikizumab
- Tralokinumab
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| IL-15 |
- Agonists: ALT-803
- Interleukin 15
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| IL-17 |
- Agonists: Interleukin 17 (A, B, C, D, E (interleukin 25), F)
- Antibodies: Brodalumab
- Ixekizumab
- Perakizumab
- Remtolumab
- Secukinumab
- Vunakizumab
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| IL-18 |
- Agonists: Iboctadekin
- Interleukin 18
- Interleukin 37
- Tadekinig
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| IL-20 |
- Agonists: Interleukin 19
- Interleukin 20
- Interleukin 24
- Antibodies: Fletikumab (against IL-20)
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| IL-21 |
- Agonists: Denenicokin
- Interleukin 21
- Antibodies: NNC0114-0005
- NNC0114-0006
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| IL-22 |
- Antibodies: Fezakinumab (against IL-22)
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| IL-23 |
- Agonists: Interleukin 23 (SGRF)
- Antibodies: Brazikumab
- Briakinumab
- Guselkumab
- Risankizumab
- Tildrakizumab
- Ustekinumab
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| IL-27 |
- Agonists: Interleukin 27 (interleukin 30)
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| IL-28 |
- Agonists: Interferon λ4 (IFN-λ4)
- Interleukin 28 (A (IFN-λ2), B (IFN-λ3))
- Interleukin-29 (IFN-λ1)
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| IL-31 | |
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| IL1RL1 | |
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| IL1RL2 |
- Agonists: Interleukin 36 (α, β, γ)
- Interleukin 38
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| Others | | JAK | |
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| Others |
- Interleukin 14 (taxilin alpha, HMW-BCGF)
- Interleukin 16 (signals through CD4)
- Interleukin 24 (signals through IL-22Rα1/IL-20Rβ heterodimer)
- Interleukin 26 (signals through IL-20Rα/IL-10Rβ heterodimer)
- Interleukin 32
- Interleukin 34 (signals through M-CSFR/CSF1R)
- Interleukin 35
- Unsorted: Efavaleukin alfa
- Efineptakin alfa
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