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Systemic management of malignant meningiomas: A comparative survival and molecular marker analysis between Octreotide
Andrés F Cardona1,2,3, Alejandro Ruiz-Patiño2, Zyanya Lucia Zatarain-Barrón4
1Brain Tumor Section, Clinical and Translational Oncology Group, Clínica del Country, Bogotá, Colombia.
Purpose:
To compare the effectiveness of octreotide/everolimus vs. sunitinib for the systemic treatment of recurrent aggressive meningiomas.
Methods:
31 patients with recurrent or refractory WHO II or WHO III meningiomas were examined in two reference centers in Colombia. Patients who had systemic treatment (sunitinib, everolimus/octreotide) and a complete follow-up were included. Overall survival (OS), progression-free survival (PFS) and toxicities were evaluated. Additionally, tissue samples were examined for PDGFRβ and VEGFR2, their expression was correlated with outcomes.
Results:
Twenty-two patients (72%) were female with a median age of 55 years (SD±15.3). The most prevalent histology was anaplastic meningioma in 20 patients (65%) with 48% of patients suffering from three previous relapses before the start of systemic treatment. A total of 14 patients received combination therapy with octreotide/everolimus, 11 received sunitinib and the remaining 6 received other second-line agents. Median OS was 37.3 months (95%CI 28.5-42.1) and the PFS during the treatment with everolimus/octreotide (EO) and sunitinib (Su) was 12.1 months (95%CI 9.2-21.1) and 9.1 months (95%CI 6.8-16.8); p = 0.43), respectively. The OS of the group treated with the EO→Su→Bev sequence (1st/2nd/3rd line) was 6.5 months longer than the Su→EO→Bev sequence (36.0 vs. 29.5 months) (p = 0.0001). When analyzing molecular markers, the positive PDGFRβ and negative VEGFR2 expression were associated with longer survival both in OS and PFS.
Conclusion:
Sunitinib and octreotide/everolimus have similar efficacy and safety in the systemic management of refractory meningioma. VEGFR2 and PDGFRβ expression are associated with better outcomes.
Insights
Octreotide/everolimus and sunitinib show similar effectiveness for treating recurrent aggressive meningiomas. Molecular markers like PDGFRβ and VEGFR2 influence patient outcomes, suggesting potential for targeted therapies.
Area of Science:
- Neuro-oncology
- Medical oncology
- Molecular pathology
Background:
- Meningiomas, particularly aggressive WHO II/III types, present challenges in recurrent or refractory settings.
- Systemic therapies are crucial for managing advanced meningioma disease.
Purpose of the Study:
- To compare the efficacy and safety of octreotide/everolimus versus sunitinib for recurrent aggressive meningiomas.
- To investigate the correlation between molecular markers (PDGFRβ, VEGFR2) and treatment outcomes.
Main Methods:
- Retrospective analysis of 31 patients with recurrent/refractory WHO II/III meningiomas across two Colombian centers.
- Evaluation of overall survival (OS), progression-free survival (PFS), and toxicities.
- Analysis of PDGFRβ and VEGFR2 expression in tissue samples.
Main Results:
- Octreotide/everolimus (n=14) and sunitinib (n=11) demonstrated comparable median PFS (12.1 vs. 9.1 months, p=0.43).
- The octreotide/everolimus→sunitinib→bevacizumab sequence showed improved OS compared to sunitinib→octreotide/everolimus→bevacizumab (36.0 vs. 29.5 months, p=0.0001).
- Positive PDGFRβ and negative VEGFR2 expression correlated with longer OS and PFS.
Conclusions:
- Octreotide/everolimus and sunitinib exhibit similar efficacy and safety profiles for refractory meningioma.
- VEGFR2 and PDGFRβ expression levels are predictive of better treatment outcomes in meningioma patients.
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