Guidance for dosing and monitoring of oral antineoplastic drugs in
breast cancer patients after bariatric surgery
- Jurjen Kingma,
- Niels Peeters,
- Catherijne Knibbe,
- Mariette Agterof,
- Wouter Derksen,
- Marcel van den Broek,
- Desirée Burgers
Jurjen Kingma
Sint Antonius Hospital
Corresponding Author:j.kingma@antoniusziekenhuis.nl
Author ProfileAbstract
Bariatric surgery is a common applied surgical intervention in
individuals with obesity to achieve weight-loss, to reduce comorbidities
and improve overall survival. However, commonly performed techniques are
associated with physiological changes in the gastrointestinal tract that
may lead to changes in oral drug disposition. Furthermore, recommended
dietary restrictions after bariatric surgery might influence drug
disposition and due to prophylactic prescribed drugs interactions might
occur. Also, in the years after bariatric surgery, patients will lose
weight. These alterations can influence oral drug disposition of oral
antineoplastic drugs and, subsequently influence outcomes of breast
cancer treatment. The purpose of this review is to provide an overview
of the available evidence on the effect of bariatric surgery on the
pharmacokinetics of oral antineoplastic drug used in breast cancer
treatment. We performed a comprehensive analysis of published
pharmacokinetic and pharmacodynamics data. Subsequently we provide,
where possible, recommendations on preferences within therapeutic
classes and provide recommendations when prescribing oral antineoplastic
drugs for breast cancer. Due to the limited availability of clinical
evidence on oral drug disposition and subsequently outcomes in this
population, our advice is to monitor patients extensively for efficacy
but also for safety before and after surgery.