Since the beginning of 2019, the ANSM has alerted health professionals and women about the risk of meningioma* associated with the use of nomigestrol (lutenyl and generics) and chlormaudinone (luteran and generic) acetate as well as their use is extended and at high dose.
In June 2020 a vast epidemiological study made it possible to quantify this risk for the first time:
- A woman who takes one of these treatments for more than six months has approximately 3.3 times more risk of developing meningioma* compared to the basic risk
- The risk increases with the duration of treatment, and also with the dose used and the age of the patient:
- Under Lotényl the risk is multiplied by 12.5 from five years of treatment
- Under Luteran, it is multiplied by 7 for 3.5 years of treatment
Given these new data, preliminary recommendations have been drawn up by an expert committee (see below).
In order to establish the appropriate measures to use these progestin drugs with regard to the risk of meningioma and the needs of women for which these treatments are justified, the ANSM organizes a public consultation on Monday, November 2, 2020.
You are or have been processed by Lotényl, Lotéran or their generics, or whether you are a health professional, consult the preliminary recommendations:
Link to the ANSM: https://www.ansm.sante.fr/dossiers/lutenyl-luteran/lutenyl-luteran-et-risque-de-meningiome/(offset)/0