Efficacy of Heptral® in the treatment of hepatic toxicity induced by cytostatic chemotherapy

The efficacy of Heptral® (ademethionine) was evaluated in the treatment of chemotherapy-induced hepatotoxicity in 19 patients with various malignancies. Four-week administration of oral Heptral® 400 mg twice daily was shown to reduce the level of transaminases to normal values in 10 of 12 patients w...

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Main Authors: A. V. Snegovoy, L. V. Manzyuk
Format: Article
Language:Russian
Published: ABV-press 2014-08-01
Series:Опухоли женской репродуктивной системы
Subjects:
Online Access:https://ojrs.abvpress.ru/ojrs/article/view/230
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author A. V. Snegovoy
L. V. Manzyuk
author_facet A. V. Snegovoy
L. V. Manzyuk
author_sort A. V. Snegovoy
collection DOAJ
description The efficacy of Heptral® (ademethionine) was evaluated in the treatment of chemotherapy-induced hepatotoxicity in 19 patients with various malignancies. Four-week administration of oral Heptral® 400 mg twice daily was shown to reduce the level of transaminases to normal values in 10 of 12 patients with grade 1 toxicity. Longer (2-to-4 month) use of Heptral® was required to normalize the level of transminases in grade 2 hepatotoxicity. The chemotherapy regimen was not changed during the use of this drug.
format Article
id doaj-art-c670bbcd60514a7fae019329ff436e4e
institution DOAJ
issn 1994-4098
1999-8627
language Russian
publishDate 2014-08-01
publisher ABV-press
record_format Article
series Опухоли женской репродуктивной системы
spelling doaj-art-c670bbcd60514a7fae019329ff436e4e2025-08-20T03:02:01ZrusABV-pressОпухоли женской репродуктивной системы1994-40981999-86272014-08-0102475210.17650/1994-4098-2010-0-2-47-52246Efficacy of Heptral® in the treatment of hepatic toxicity induced by cytostatic chemotherapyA. V. Snegovoy0L. V. Manzyuk1N.N. Blokhin Russian Cancer Research Center, Russian Academy of Medical Sciences, MoscowN.N. Blokhin Russian Cancer Research Center, Russian Academy of Medical Sciences, MoscowThe efficacy of Heptral® (ademethionine) was evaluated in the treatment of chemotherapy-induced hepatotoxicity in 19 patients with various malignancies. Four-week administration of oral Heptral® 400 mg twice daily was shown to reduce the level of transaminases to normal values in 10 of 12 patients with grade 1 toxicity. Longer (2-to-4 month) use of Heptral® was required to normalize the level of transminases in grade 2 hepatotoxicity. The chemotherapy regimen was not changed during the use of this drug.https://ojrs.abvpress.ru/ojrs/article/view/230chemotherapyhepatotoxicitytransaminaseademethionine
spellingShingle A. V. Snegovoy
L. V. Manzyuk
Efficacy of Heptral® in the treatment of hepatic toxicity induced by cytostatic chemotherapy
Опухоли женской репродуктивной системы
chemotherapy
hepatotoxicity
transaminase
ademethionine
title Efficacy of Heptral® in the treatment of hepatic toxicity induced by cytostatic chemotherapy
title_full Efficacy of Heptral® in the treatment of hepatic toxicity induced by cytostatic chemotherapy
title_fullStr Efficacy of Heptral® in the treatment of hepatic toxicity induced by cytostatic chemotherapy
title_full_unstemmed Efficacy of Heptral® in the treatment of hepatic toxicity induced by cytostatic chemotherapy
title_short Efficacy of Heptral® in the treatment of hepatic toxicity induced by cytostatic chemotherapy
title_sort efficacy of heptral r in the treatment of hepatic toxicity induced by cytostatic chemotherapy
topic chemotherapy
hepatotoxicity
transaminase
ademethionine
url https://ojrs.abvpress.ru/ojrs/article/view/230
work_keys_str_mv AT avsnegovoy efficacyofheptralinthetreatmentofhepatictoxicityinducedbycytostaticchemotherapy
AT lvmanzyuk efficacyofheptralinthetreatmentofhepatictoxicityinducedbycytostaticchemotherapy