Difference between revisions of "Afatinib (Gilotrif)"
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==History of changes in FDA indication== | ==History of changes in FDA indication== | ||
| − | *7/12/2013: [http://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm360574.htm Approved] for the first-line treatment of patients with metastatic [[Non-small_cell_lung_cancer | + | *7/12/2013: [http://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm360574.htm Approved] for the first-line treatment of patients with metastatic [[Non-small_cell_lung_cancer|non-small cell lung cancer (NSCLC)]] whose tumors have epidermal growth factor receptor [[Biomarkers#EGFR|EGFR]] exon 19 [[#Biomakers_Structural Variant|deletion]] or exon 21 (L858R) [[#Biomakers_SNV|substitution]] mutations as detected by an FDA-approved test. |
*4/15/2016: Approved for treatment of patients with metastatic, [[Non-small_cell_lung_cancer|squamous NSCLC]] progressing after platinum-based chemotherapy. | *4/15/2016: Approved for treatment of patients with metastatic, [[Non-small_cell_lung_cancer|squamous NSCLC]] progressing after platinum-based chemotherapy. | ||
| − | *1/12/2018: Approval expanded for a broadened indication in first-line treatment of patients with metastatic [[Non-small_cell_lung_cancer | + | *1/12/2018: Approval expanded for a broadened indication in first-line treatment of patients with metastatic [[Non-small_cell_lung_cancer|non-small cell lung cancer (NSCLC)]] whose tumors have non-resistant epidermal growth factor receptor [[Biomarkers#EGFR|EGFR]] as detected by an FDA-approved test. |
==Also known as== | ==Also known as== | ||
Revision as of 00:11, 9 January 2020
General information
Class/mechanism: Irreversible tyrosine kinase inhibitor of EGFR (epidermal growth factor receptor, ErbB1), HER2 (human epidermal growth factor receptor 2, ErbB2), and HER4 (human epidermal growth factor receptor 4, ErbB4). Inhibition of tyrosine kinase autophosphorylation inhibits ErbB signaling.[1][2][3]
Route: PO
Extravasation: n/a
For conciseness and simplicity, HemOnc.org currently will focus on treatment regimens and not list information such as: renal/hepatic dose adjustments, metabolism (including CYP450), excretion, monitoring parameters (although this will be considered for checklists), or manufacturer. Instead, for the most current information, please refer to your preferred pharmacopeias such as Micromedex, Lexicomp, UpToDate (courtesy of Lexicomp), or the prescribing information.[1]
Diseases for which it is used
Patient drug information
- Afatinib (Gilotrif) package insert[1]
- Afatinib (Gilotrif) patient drug information (Chemocare)[4]
- Afatinib (Gilotrif) patient drug information (UpToDate)[5]
History of changes in FDA indication
- 7/12/2013: Approved for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors have epidermal growth factor receptor EGFR exon 19 deletion or exon 21 (L858R) substitution mutations as detected by an FDA-approved test.
- 4/15/2016: Approved for treatment of patients with metastatic, squamous NSCLC progressing after platinum-based chemotherapy.
- 1/12/2018: Approval expanded for a broadened indication in first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors have non-resistant epidermal growth factor receptor EGFR as detected by an FDA-approved test.
Also known as
- Code names: BIBW 2992, BIBW-2992
- Brand names: Afanix, Gilotrif, Giotrif, Tomtovok, Tovok, Xovoltib