TY - JOUR
T1 - Prognostic significance of telomerase reverse transcriptase promoter mutations in high grade meningiomas
AU - Cañas, Alejandro
AU - Jiménez, Enrique
AU - Hakim, Fernando
AU - Mejía, Juan Armando
AU - Ramón, Juan Fernando
AU - Gómez, Diego
AU - Jaramillo-Velásquez, Daniel
AU - Bermúdez, Sonia
AU - Useche, Nicolás
AU - Pineda, Diego
AU - Cifuentes, Hernando
AU - Becerra, Antonio
AU - Muñoz, Álvaro
AU - Santoyo, Nicolás
AU - Ruíz-Patiño, Alejandro
AU - Sotelo, Carolina
AU - Archila, Pilar
AU - Rodríguez, July
AU - Ávila, Jenny
AU - Ordóñez-Reyes, Camila
AU - García-Robledo, Juan Esteban
AU - Ricaurte, Luisa
AU - Rojas, Leonardo
AU - Feo, Oscar
AU - Burgos, Remberto
AU - Ramírez, Carlos
AU - Arrieta, Oscar
AU - Zatarain-Barrón, Lucía
AU - Vargas, Carlos
AU - Carranza, Hernán
AU - Otero, Jorge
AU - Cardona, Andrés F.
N1 - Publisher Copyright:
© 2022, Biomedica. All Rights Reserved.
PY - 2022
Y1 - 2022
N2 - Introduction: Mutations in the promoter region of telomerase reverse transcriptase occur frequently in meningiomas. Objective: To estimate the prognostic value of telomerase reverse transcriptase mutations in Colombian patients with grade II and III meningioma. Materials and methods: Multicenter retrospective cohort study of patients diagnosed with refractory or recurrent WHO grade II and III meningioma, recruited between 2011 and 2018, managed with systemic therapy (sunitinib, everolimus +/- octreotide and bevacizumab). Mutation status of the telomerase reverse transcriptase promoter was performed by PCR. Results: 40 patients were included, of which telomerase reverse transcriptase mutations were found in 21 (52.5%), the most frequent variants being C228T and C250T, 87.5% and 14.3%, respectively. These were more frequent among patients with anaplastic meningiomas (p = 0.18), with >2 recurrences (p = 0.04), and in lesions of the parasagittal region and anterior fossa (p = 0.05). Subjects characterized as having punctual alterations were more frequently exposed to the sequence E → Su → Bev (p = 0.06). OS after initiation of medical treatment was 23.7 months (95% CI 13.1-34.2) and 43.4 months (95% CI 37.5-49.3; p = 0.0001) between subjects with and without mutations, respectively. In multivariate analysis, it was shown that only the number of recurrences and the presence of telomerase reverse transcriptase mutations negatively affected OS. Conclusions: Telomerase reverse transcriptase allows identifying high-risk patients and could be useful to select the best sequence of medical treatment.
AB - Introduction: Mutations in the promoter region of telomerase reverse transcriptase occur frequently in meningiomas. Objective: To estimate the prognostic value of telomerase reverse transcriptase mutations in Colombian patients with grade II and III meningioma. Materials and methods: Multicenter retrospective cohort study of patients diagnosed with refractory or recurrent WHO grade II and III meningioma, recruited between 2011 and 2018, managed with systemic therapy (sunitinib, everolimus +/- octreotide and bevacizumab). Mutation status of the telomerase reverse transcriptase promoter was performed by PCR. Results: 40 patients were included, of which telomerase reverse transcriptase mutations were found in 21 (52.5%), the most frequent variants being C228T and C250T, 87.5% and 14.3%, respectively. These were more frequent among patients with anaplastic meningiomas (p = 0.18), with >2 recurrences (p = 0.04), and in lesions of the parasagittal region and anterior fossa (p = 0.05). Subjects characterized as having punctual alterations were more frequently exposed to the sequence E → Su → Bev (p = 0.06). OS after initiation of medical treatment was 23.7 months (95% CI 13.1-34.2) and 43.4 months (95% CI 37.5-49.3; p = 0.0001) between subjects with and without mutations, respectively. In multivariate analysis, it was shown that only the number of recurrences and the presence of telomerase reverse transcriptase mutations negatively affected OS. Conclusions: Telomerase reverse transcriptase allows identifying high-risk patients and could be useful to select the best sequence of medical treatment.
KW - Gain of function mutation
KW - Meningioma
KW - Telomerase
UR - http://www.scopus.com/inward/record.url?scp=85137288068&partnerID=8YFLogxK
U2 - 10.7705/biomedica.6100
DO - 10.7705/biomedica.6100
M3 - Article
C2 - 36511679
AN - SCOPUS:85137288068
SN - 0120-4157
VL - 42
JO - Biomedica
JF - Biomedica
IS - 4
ER -