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Carboplatin-gemcitabine for refractory high-grade meningiomas: A study from the French national OMEGA consortium
Mathieu Larroquette1,2, Charlotte Bronnimann1, Morgan Ollivier3
1Department of Medical Oncology, Hôpital Saint André, CHU de Bordeaux, Bordeaux, France.
Abstract:
High-grade meningiomas are rare tumours that often relapse and are difficult to treat, and no clearly recommended systemic treatment is available. In this study, we assessed the efficacy of carboplatin-gemcitabine as a systemic chemotherapy regimen administered to patients with high-grade recurrent meningiomas after observing incidental tumour shrinkage in one patient. Carboplatin-gemcitabine was offered on a compassionate basis to French patients with high-grade recurrent meningioma within the framework of the French Réunion d'orientation thérapeutique des méningiomes de haut grade (OMEGA) multidisciplinary board, which discusses all meningioma cases nationwide that are not amenable to standard treatment (surgery or radiotherapy). We retrospectively analysed the efficacy of this treatment in French patients from 2019 to 2023. We evaluated the three-dimensional volumetric kinetics of the tumour, progression-free survival (PFS), and safety. Carboplatin-gemcitabine slowed tumour growth for several months in some heavily pretreated patients despite the failure of previous systemic therapies. The 6-month PFS rate for the cohort of six patients was 50% (95% confidence interval, [22.5-100%]). Safety was characterised by asthenia and manageable haematological toxicity. Our results provide encouraging data on the efficacy of carboplatin-gemcitabine for meningiomas and should be validated in a prospective trial. Despite the small number of patients, our study included all French patients treated for a 4-year period and should be considered alongside other previously published studies, which also included few patients due to the rarity of the disease. Our findings highlight the importance of national networks for managing these patients and the need for multicentre trials.
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