2008
DOI: 10.1345/aph.1l410
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Syndrome of Inappropriate Secretion of Antidiuretic Hormone Associated with Imatinib

Abstract: We recommend monitoring for SIADH if a patient receiving high-dose imatinib develops hyponatremia.

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Cited by 27 publications
(20 citation statements)
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References 21 publications
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“…7 In a previously reported case of SIADH due to imatinib, the authors theorized the patient could have experienced increased plasma concentrations of imatinib due to concurrent administration of omeprazole (a cytochrome P450 (CYP) 3A4 substrate and weak inhibitor and p-glycoprotein (P-gp) substrate inhibitor) and imatinib which is primarily metabolized by CYP 3A4 and also a P-gp substrate and inhibitor. 2 Using this theory, it is reasonable to assume a similar interaction could have occurred with our patient who was also receiving a proton-pump inhibitor, rabeprazole. The degree of interaction would theoretically be less with rabeprazole as it is thought to have less CYP3A4 metabolism than omeprazole; however, this increased drug exposure could have led to the SIADH experienced by the patient.…”
Section: Discussionmentioning
confidence: 80%
“…7 In a previously reported case of SIADH due to imatinib, the authors theorized the patient could have experienced increased plasma concentrations of imatinib due to concurrent administration of omeprazole (a cytochrome P450 (CYP) 3A4 substrate and weak inhibitor and p-glycoprotein (P-gp) substrate inhibitor) and imatinib which is primarily metabolized by CYP 3A4 and also a P-gp substrate and inhibitor. 2 Using this theory, it is reasonable to assume a similar interaction could have occurred with our patient who was also receiving a proton-pump inhibitor, rabeprazole. The degree of interaction would theoretically be less with rabeprazole as it is thought to have less CYP3A4 metabolism than omeprazole; however, this increased drug exposure could have led to the SIADH experienced by the patient.…”
Section: Discussionmentioning
confidence: 80%
“…Tyrosine Kinase Inhibitors (TKI) treatment has been associated with SIADH. Hyponatremia-related SIADH was reported in patients affected by Bcr-Abl acute lymphoblastic leukemia treated by Imatinib at a dose of 400 mg/day, and was observed after 11 months of therapy (81), in those affected by refractory chronic myelogenous leukemia treated with Dasatinib (100 mg/day), Nilotinib (400 mg twice/day) and Bosutinib (500 mg/day) (82), as well as in patients with renal carcinoma or with metastatic head and neck cancer treated with Sorafenib (400 mg twice/day for a median duration of therapy of 3.4 months) (83). Mammalian targets of rapamycin (mTOR) inhibitors.…”
Section: Target Therapiesmentioning
confidence: 99%
“…Other causes of SIADH include surgery (intense pain and post‐operative nausea stimulate secretion of AVP) and drugs. Among the most commonly drugs are antidepressants (amitriptyline, citalopram and fluoxetine), non‐steroidal anti‐inflammatory drugs, chlorpropamide, tolbutamide, clofibrate, cyclophosphamide, ciprofloxacin, interferon‐alpha, interferon‐gamma, carbamazepine, amiodarone, morphine, amphetamines and ‘ecstasy’ …”
Section: Resultsmentioning
confidence: 99%