Tyrosine Kinase Inhibitor Pharmacokinetics

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (09:12, 11 December 2010) (edit) (undo)
 
(9 intermediate revisions not shown.)
Line 1: Line 1:
{| class="wikitable" border="0" width="100%" style="text-align:center"
{| class="wikitable" border="0" width="100%" style="text-align:center"
|-
|-
-
! colspan="6" align="center"| Tyrosine Kinase Inhibitor [[Pharmacokinetics]]
+
! colspan="9" align="center"| Tyrosine Kinase Inhibitor [[Pharmacokinetics]]
|-
|-
! colspan="1" align="center"|
! colspan="1" align="center"|
! colspan="2" align="center"| [[VEGFR]] & KIT Inhibitors
! colspan="2" align="center"| [[VEGFR]] & KIT Inhibitors
! colspan="3" align="center"| [[EGFR]] Inhibitors
! colspan="3" align="center"| [[EGFR]] Inhibitors
-
! colspan="1" align="center"| PDGFR Inhibitor
+
! colspan="3" align="center"| BCR-Abl Inhibitor
|-
|-
! Parameter
! Parameter
Line 15: Line 15:
! [[Lapatinib]]<br/>(Tykerb)
! [[Lapatinib]]<br/>(Tykerb)
! [[Imatinib]]<br/>(Gleevec)
! [[Imatinib]]<br/>(Gleevec)
 +
! [[Nilotinib]]<br/>(Tasigna)
 +
! [[Dasatinib]]<br/>(Sprycel)
|-
|-
! [[Pharmacokinetics#Tmax|T<sub>max</sub>]] (hr)
! [[Pharmacokinetics#Tmax|T<sub>max</sub>]] (hr)
Line 22: Line 24:
! 5.4
! 5.4
! 4
! 4
-
! [[Imatinib]]<br/>(Gleevec)
+
! 3.7
 +
! 3.0
 +
! 1.0
|-
|-
! [[Pharmacokinetics#Cmax|C<sub>max</sub>]] (ng/ml)
! [[Pharmacokinetics#Cmax|C<sub>max</sub>]] (ng/ml)
Line 30: Line 34:
! 130
! 130
! 115
! 115
-
! [[Imatinib]]<br/>(Gleevec)
+
! 2070
 +
! 411
 +
! 124
|-
|-
! [[Pharmacokinetics#Bioavailability_.28F.29|Bioavailability]] (%)
! [[Pharmacokinetics#Bioavailability_.28F.29|Bioavailability]] (%)
Line 38: Line 44:
! 59
! 59
! Variable
! Variable
-
! [[Imatinib]]<br/>(Gleevec)
+
! 98
 +
! 30
 +
! 20
|-
|-
! [[Pharmacokinetics#Protein_Binding|Protein Binding]] (%)
! [[Pharmacokinetics#Protein_Binding|Protein Binding]] (%)
Line 46: Line 54:
! 90
! 90
! 99
! 99
-
! [[Imatinib]]<br/>(Gleevec)
+
! 95
 +
! 98
 +
! 96
|-
|-
! [[Pharmacokinetics#Half_Life_.28T1.2F2.29|T<sub>1/2</sub>]] (hr)
! [[Pharmacokinetics#Half_Life_.28T1.2F2.29|T<sub>1/2</sub>]] (hr)
Line 54: Line 64:
! 26.9
! 26.9
! 9.6
! 9.6
-
! [[Imatinib]]<br/>(Gleevec)
+
! 26.6
 +
! 16.0
 +
! 3.3
|-
|-
! [[Pharmacokinetics#Area_Under_the_Curve_.28AUC.29|AUC]] (ng/ml/hr)
! [[Pharmacokinetics#Area_Under_the_Curve_.28AUC.29|AUC]] (ng/ml/hr)
Line 62: Line 74:
! 3850
! 3850
! 1429
! 1429
-
! [[Imatinib]]<br/>(Gleevec)
+
! 4760
 +
! 10052
 +
! 461
|-
|-
! Dosage (mg)
! Dosage (mg)
Line 70: Line 84:
! 250
! 250
! 100
! 100
-
! [[Imatinib]]<br/>(Gleevec)
+
! 400
 +
! 200
 +
! 200
|-
|-
! Metabolism
! Metabolism
! Hepatic (CYP3A4)
! Hepatic (CYP3A4)
! Hepatic (CYP3A4)
! Hepatic (CYP3A4)
-
! Hepatic - (CYP3A4)
+
! Hepatic (CYP3A4)
-
! Hepatic - (CYP3A4)
+
! Hepatic (CYP3A4)
-
! Hepatic - (CYP3A4)
+
! Hepatic (CYP3A4)
-
! [[Imatinib]]<br/>(Gleevec)
+
! Hepatic (CYP3A4)
 +
! Hepatic (CYP3A4)
 +
! Hepatic (CYP3A4)
|}
|}
-
For references see: [[TYKI_References|References]]
+
For Pharmacokinetic Data References, see: [[Treatments:TYKI References|References]]

Current revision

Tyrosine Kinase Inhibitor Pharmacokinetics
VEGFR & KIT Inhibitors EGFR Inhibitors BCR-Abl Inhibitor
Parameter Sunitinib
(Sutent)
Sorafenib
(Nexavar)
Erlotinib
(Tarceva)
Gefitinib
(Iressa)
Lapatinib
(Tykerb)
Imatinib
(Gleevec)
Nilotinib
(Tasigna)
Dasatinib
(Sprycel)
Tmax (hr) 8 8.3 2.0 5.4 4 3.7 3.0 1.0
Cmax (ng/ml) 24.6 460 69.6 130 115 2070 411 124
Bioavailability (%) Variable 29-49 99 59 Variable 98 30 20
Protein Binding (%) 95 99 93 90 99 95 98 96
T1/2 (hr) 83 29 9.4 26.9 9.6 26.6 16.0 3.3
AUC (ng/ml/hr) 1921 11040 20577 3850 1429 4760 10052 461
Dosage (mg) 50 50 150 250 100 400 200 200
Metabolism Hepatic (CYP3A4) Hepatic (CYP3A4) Hepatic (CYP3A4) Hepatic (CYP3A4) Hepatic (CYP3A4) Hepatic (CYP3A4) Hepatic (CYP3A4) Hepatic (CYP3A4)

For Pharmacokinetic Data References, see: References

Proteopedia Page Contributors and Editors (what is this?)

David Canner

Personal tools