A dose-dependent relationship between meningioma incidence and growth and hormonal treatment with cyproterone acetate has been established, with similar but lower risks reported for chlormadinone acetate and nomegestrol acetate, while evidence for oral contraceptives does not support increased meningioma risk.
Key Findings
Background
A dose-dependent relationship between the incidence and growth of meningiomas and hormonal treatment with cyproterone acetate (CPA) has been established.
CPA is a progestin used in hormonal treatments
The relationship is described as dose-dependent, implicating both duration and amount of CPA use
More common meningioma occurrence is associated with longer duration of treatment
This represents a recently established finding based on accumulated study data
Results
CPA-associated meningiomas have distinct clinical and molecular characteristics compared to sporadic meningiomas.
CPA-associated meningiomas are mainly located in the anterior and middle skull base
They are more likely to be multiple rather than solitary
PIK3CA mutations may be present in up to one-third of cases
These features distinguish CPA-associated meningiomas from typical sporadic meningiomas
Results
Chlormadinone acetate and nomegestrol acetate are associated with a similar but lower risk of meningiomas compared to CPA.
Both chlormadinone acetate and nomegestrol acetate are progestin treatments
The risk of meningioma with these agents is described as 'similar but lower' than that seen with CPA
These findings were recently reported in the literature
The finding extends the progestin class association with meningioma risk beyond CPA alone
Results
Epidemiological evidence suggests an increased risk of meningiomas in menopausal patients receiving hormonal replacement therapy (HRT), though one study failed to show increased tumor growth.
Evidence from epidemiological studies favors an increased risk of meningiomas in HRT-treated patients
A recent study failed to show increased growth of meningiomas in HRT-treated versus nontreated patients
The authors recommend avoiding HRT in patients with meningiomas until larger studies are available
The evidence is described as conflicting between incidence risk and growth outcomes
Results
Published data do not support an increased risk of meningiomas with oral contraceptive use.
Evidence from published data does not seem to support an increased risk of meningiomas with oral contraceptive use
This finding contrasts with the established risk seen with higher-dose progestin treatments such as CPA
Data on fertility treatments are described as too scarce to draw conclusions
Results
Therapies targeting hormonal receptors expressed in meningiomas have failed to show an overall favorable clinical outcome.
Hormonal receptors have been demonstrated to be expressed in meningiomas
Based on receptor expression studies, therapies targeting these receptors have been tried
These receptor-targeted therapies have failed to show an overall favorable clinical outcome in meningioma treatment
Meningiomas have a well-documented female predominance, which has long suggested a role for sex hormones in their etiology
Hage M, Plesa O, Lemaire I, Raffin Sanson M. (2022). Estrogen and Progesterone Therapy and Meningiomas.. Endocrinology. https://doi.org/10.1210/endocr/bqab259