Détail du document
Identifiant

oai:pubmedcentral.nih.gov:9953...

Sujet
Article
Auteur
Breuer, Olof Brodin, Ola Razaghi, Ali Brodin, David Gammelgaard, Bente Björnstedt, Mikael
Langue
en
Editeur

MDPI

Catégorie

Biomedicines

Année

2023

Date de référencement

29/11/2023

Mots clés
trial cancer selenium detected patients
Métrique

Résumé

Cancer is one of the main causes of human death globally and novel chemotherapeutics are desperately required.

As a simple selenium oxide, selenite is a very promising chemotherapeutic because of pronounced its dose-dependent tumor-specific cytotoxicity.

We previously published a first-in-man systematic phase I clinical trial in patients with cancer (from IV to end-stage) (the SECAR trial) showing that selenite is safe and tolerable with an unexpectable high maximum tolerated dose (MTD) and short half-life.

In the present study, we analyzed the selenium species in plasma samples, from the patients participating in the SECAR trial and from various time points and dose cohorts using LC-ICP-MS.

In conclusion, selenite, selenosugars, and 1–2 unidentified peaks that did not correspond to any standard, herein denoted ui-selenium, were detected in the plasma.

However, trimethylated selenium (trimethylselenonoium) was not detected.

The unidentified ui-selenium was eluting close to the selenium-containing amino acids (selenomethionine and selenocysteine) but was not part of a protein fraction.

Our data demonstrate that the major metabolite detected was selenosugar.

Furthermore, the identification of selenite even long after the administration is remarkable and unexpected.

The kinetic analysis did not support that dosing per the body surface area would reduce interindividual variability of the systemic exposure in terms of trough concentrations.

Breuer, Olof,Brodin, Ola,Razaghi, Ali,Brodin, David,Gammelgaard, Bente,Björnstedt, Mikael, 2023, Intravenous Infusion of High Dose Selenite in End-Stage Cancer Patients: Analysis of Systemic Exposure to Selenite and Seleno-Metabolites, MDPI

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