To systematically assess the risk of meningioma associated with various progestogens used in contraception, considering timing of use, pregnancy, and prior hormone replacement therapy.
Approach:
Study Design: A nested case-control study using nationwide Danish registers to identify cases of meningioma among females aged 15 to 59 years, matched with controls.
Data Sources: Data was collected from the Danish National Prescription Register, National Patient Register, and National Hospital Medication Register.
Exposure Assessment: Hormonal contraceptives were categorized by type and route of administration, with exposure defined by prescription dispensing dates and treatment durations.
Key Findings:
Meningioma is the most common intracranial tumor in adults, representing 38% to 42% of all primary central nervous system tumors.
Population-based data from the United States show an incidence rate of 10.15 per 100,000 persons overall, with rates of 13.90 and 6.02 for women and men, respectively.
In Denmark, the incidence is 12.6 per 100,000 persons overall, with 17.9 and 7.4 per 100,000 for women and men, respectively.
Progesterone receptors are present in up to 87% of meningiomas, suggesting a hormonal influence.
Conflicting evidence exists regarding the association between hormonal contraceptives and meningioma risk.
Interpretation:
The study aims to clarify the relationship between progestogen use in contraception and meningioma risk, addressing gaps in existing literature.
Limitations:
Meningioma is rare among women of reproductive age, leading to small exposure groups.
The study relies on existing health registers, which may have limitations in data completeness and accuracy.
Conclusion:
This study represents a comprehensive assessment of meningioma risk associated with various progestogens in a defined female population.
Dana-Farber Cancer Institute's Dr. Sara Tolaney presented a subgroup analysis of the ASCENT-04 study based on biomarkers. Across all subgroups, patients who received sacituzumab govitecan plus pembro as first-line therapy had longer progression-free survival compared to standard therapy.