Open Access Articles- Top Results for Afatinib


Systematic (IUPAC) name
Clinical data
Trade names Gilotrif, Giotrif
AHFS/ Multum Consumer Information
Licence data EMA:Link, US FDA:link
  • AU: C
  • US: D (Evidence of risk)
Pharmacokinetic data
Bioavailability ?
Protein binding 95%
Metabolism CYP not involved
Half-life 37 hours
Excretion Faeces (85%), urine (4%)
850140-72-6 7pxY[Drugbank]
PubChem CID 10184653
DrugBank DB08916 7pxY
ChemSpider 8360155 7pxY
UNII 41UD74L59M 7pxY
ChEBI CHEBI:61390 7pxY
ChEMBL CHEMBL1173655 7pxY
Synonyms BIBW 2992
Chemical data
Formula C24H25ClFN5O3
485.937 g/mol
 14pxY (what is this?)  (verify)

Afatinib[1] (INN; trade name Gilotrif in the US and Giotrif in Europe, previously Tomtovok and Tovok[2]) is a drug approved in United States, Europe, Taiwan, Mexico, Chile and Japan as well as other countries for the first-line treatment of patients with distinct types of metastatic (EGFR mutation positive) non-small cell lung carcinoma (NSCLC), developed by Boehringer Ingelheim.[3][4][5] It acts as an irreversible covalent inhibitor of the receptor tyrosine kinases epidermal growth factor receptor (EGFR) and erbB-2 (HER2).

Medical uses

It has received regulatory approval for use as a treatment for non-small cell lung cancer,[6][7][8][9] although there is emerging evidence to support its use in other cancers such as breast cancer.[10]

In October 2010 a Phase III trial in NSCLC patients called Lux-Lung 5 began with this drug.[11] Fall 2010 interim results suggested the drug extended progression-free survival threefold compared to placebo, but did not extend overall survival.[12] In May 2012, the Phase IIb/III trial Lux-Lung 1 came to the same conclusion.[13]

Phase II results for breast cancer that over-expresses the protein human epidermal growth factor receptor 2 (Her2-positive breast cancer) were described as promising by the authors, with 19 of 41 patients achieving benefit from afatinib.[10] Double-blind Phase III trials are under way to confirm or refute this finding. Her2-negative breast cancers showed limited or no response to the drug.[14]

Adverse effects

Adverse effects by frequency:[6][7][8][15][9]

Very common (>10% frequency):

Common (1–10% frequency):

Uncommon (0.1-1% frequency):

Mechanism of action

Like lapatinib and neratinib, afatinib is a tyrosine kinase inhibitor (TKI) that also irreversibly inhibits human epidermal growth factor receptor 2 (Her2) and epidermal growth factor receptor (EGFR) kinases. Afatinib is not only active against EGFR mutations targeted by first generation TKIs like erlotinib or gefitinib, but also against those not sensitive to these standard therapies.[citation needed] Because of its additional activity against Her2, it is being investigated for breast cancer as well as other EGFR and Her2 driven cancers.[4]


  1. ^ "Afatinib (BIBW 2992) triples progression free survival in phase III study in lung cancer patients". World Pharma News. 12 October 2010. 
  2. ^ "Afatinib (BIBW-2992, Tomtovok) wins a battle (PFS) but loses the war (OS) for EGFR TKI-sensitive patients". GRACE. 18 October 2010. 
  3. ^ H. Spreitzer (13 May 2008). "Neue Wirkstoffe – Tovok". Österreichische Apothekerzeitung (in German) (10/2008): 498. 
  4. ^ a b Minkovsky N, Berezov A (December 2008). "BIBW-2992, a dual receptor tyrosine kinase inhibitor for the treatment of solid tumors". Curr Opin Investig Drugs 9 (12): 1336–46. PMID 19037840. 
  5. ^ "Afatinib". US Food and Drug Administration. 12 July 2013. 
  6. ^ a b "GILOTRIF (afatinib) tablet, film coated [Boehringer Ingelheim Pharmaceuticals, Inc.]". DailyMed. Boehringer Ingelheim Pharmaceuticals, Inc. November 2013. Retrieved 28 January 2014. 
  7. ^ a b "GIOTRIF® Afatinib (as afatinib dimaleate)" (PDF). TGA eBusiness Services. Boehringer Ingelheim Pty Limited. 7 November 2013. Retrieved 28 January 2014. 
  8. ^ a b "Giotrif 20 mg film-coated tablets – Summary of Product Characteristics (SPC)". electronic Medicines Compendium. Boehringer Ingelheim Limited. 20 January 2014. Retrieved 28 January 2014. 
  9. ^ a b "Giotrif : EPAR -Product Information" (PDF). European Medicines Agency. Boehringer Ingelheim International GmbH. 16 October 2013. Retrieved 28 January 2014. 
  10. ^ a b Lin NU, Winer EP, Wheatley D, Carey LA, Houston S, Mendelson D, Munster P, Frakes L, Kelly S, Garcia AA, Cleator S, Uttenreuther-Fischer M, Jones H, Wind S, Vinisko R, Hickish T (2012). "A phase II study of afatinib (BIBW 2992), an irreversible ErbB family blocker, in patients with HER2-positive metastatic breast cancer progressing after trastuzumab". Breast Cancer Research and Treatment 133 (3): 1057–65. PMC 3387495. PMID 22418700. doi:10.1007/s10549-012-2003-y. 
  11. ^ Clinical trial number NCT01085136 for "LUX-Lung 5: BIBW 2992 Plus Weekly Paclitaxel Versus Investigator's Choice of Single Agent Chemotherapy Following BIBW 2992 Monotherapy in Non-small Cell Lung Cancer Patients Failing Erlotinib or Gefitinib" at
  12. ^ "Afatinib (BIBW 2992*) Triples Progression Free Survival in Phase III Study in Lung Cancer Patients". BusinessWire. 11 October 2010. 
  13. ^ Miller VA, Hirsh V, Cadranel J, Chen YM, Park K, Kim SW, Zhou C, Su WC, Wang M, Sun Y, Heo DS, Crino L, Tan EH, Chao TY, Shahidi M, Cong XJ, Lorence RM, Yang JC (2012). "Afatinib versus placebo for patients with advanced, metastatic non-small-cell lung cancer after failure of erlotinib, gefitinib, or both, and one or two lines of chemotherapy (LUX-Lung 1): A phase 2b/3 randomised trial". The lancet oncology 13 (5): 528–38. PMID 22452896. doi:10.1016/S1470-2045(12)70087-6. 
  14. ^ Schuler M, Awada A, Harter P, Canon JL, Possinger K, Schmidt M, De Grève J, Neven P, Dirix L, Jonat W, Beckmann MW, Schütte J, Fasching PA, Gottschalk N, Besse-Hammer T, Fleischer F, Wind S, Uttenreuther-Fischer M, Piccart M, Harbeck N (2012). "A phase II trial to assess efficacy and safety of afatinib in extensively pretreated patients with HER2-negative metastatic breast cancer". Breast cancer research and treatment 134 (3): 1149–59. PMC 3409367. PMID 22763464. doi:10.1007/s10549-012-2126-1. 
  15. ^ "Gilotrif (afatinib) dosing, indications, interactions, adverse effects, and more". Medscape Reference. WebMD. Retrieved 28 January 2014. 
  16. ^ Schubert-Zsilavecz, M, Wurglics, M, Neue Arzneimittel Frühjahr 2013. Invalid language code.