𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Fatal liver failure after the administration of raltitrexed for cancer chemotherapy : A report of two cases

✍ Scribed by Markus Raderer; Wolfgang Fiebiger; Friedrich Wrba; Werner Scheithauer


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
53 KB
Volume
89
Category
Article
ISSN
0008-543X

No coin nor oath required. For personal study only.

✦ Synopsis


Background:

Acute fatal liver failure is a relatively rare event after the administration of antineoplastic drugs. to the authors' knowledge, there have been no published reports of this phenomenon after the administration of the widely applied cytotoxic agent raltitrexed.

Methods:

The authors present two cases of fulminant fatal liver failure that occurred after the administration of raltitrexed as anticancer chemotherapy.

Results:

A female patient age 76 years and a male patient age 56 years were given raltitrexed as adjuvant treatment of colorectal carcinoma and as palliative therapy for advanced biliary carcinoma, respectively. although the initial cycles of chemotherapy were uneventful, both patients developed fulminant liver failure with rapid deterioration of their condition after the second and sixth cycles of chemotherapy, respectively, and both died within 24 hours despite immediate hospitalization. histologic evaluation of liver samples taken during autopsy showed signs of acute necrosis involving roughly 50% of the liver without signs of subacute liver toxicity.

Conclusions:

To the authors' knowledge the current study is the first to demonstrate fatal liver toxicity after chemotherapy with the thymidylate synthase inhibitor raltitrexed. clinicians should be aware of the potential acute fatal side effect of this otherwise well tolerated and widely used cytotoxic agent.


πŸ“œ SIMILAR VOLUMES


Venoocclusive disease of the liver after
✍ Jorge A. Ortega; Sarah S. Donaldson; S. Percy Ivy; Alberto Pappo; Harold M. Maur πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 75 KB πŸ‘ 1 views

after allogenic and autologous bone marrow transplantation for malignant disease.