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ATRT-06. Atypical Teratoid Rhabdoid Tumors (ATRT): results from a Single Institution in Brazil - São Paulo University

OBJECTIVES: Atypical teratoid/rhabdoid tumor (AT/RT) is a rare, highly malignant tumor of the central nervous system with poor prognosis. Nowadays, multimodal management, including surgery, chemotherapy (CMT), radiation therapy (RT) and Bone Marrow Transplantation (BMT). The aim of this study was to...

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Autores principales: Barreto, Juliana Silveira, Gomez, Karen Nirit Melo, Dutra, Alvaro Pimenta, De Azambuja, Alessandra Milani Prandini, Cristofani, Lilian Maria, Sanders, Felipe Hada, Petito, Carlo, Baraldi, Helena Espindola, Weltman, Eduardo, Ferraciolli, Suely Fazio, Frassetto, Fernando Pereira, Lucato, Leandro Tavares, Rosemberg, Sérgio, Filho, Vicente Odone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9165313/
http://dx.doi.org/10.1093/neuonc/noac079.005
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author Barreto, Juliana Silveira
Gomez, Karen Nirit Melo
Dutra, Alvaro Pimenta
De Azambuja, Alessandra Milani Prandini
Cristofani, Lilian Maria
Sanders, Felipe Hada
Petito, Carlo
Baraldi, Helena Espindola
Weltman, Eduardo
Ferraciolli, Suely Fazio
Frassetto, Fernando Pereira
Lucato, Leandro Tavares
Rosemberg, Sérgio
Filho, Vicente Odone
author_facet Barreto, Juliana Silveira
Gomez, Karen Nirit Melo
Dutra, Alvaro Pimenta
De Azambuja, Alessandra Milani Prandini
Cristofani, Lilian Maria
Sanders, Felipe Hada
Petito, Carlo
Baraldi, Helena Espindola
Weltman, Eduardo
Ferraciolli, Suely Fazio
Frassetto, Fernando Pereira
Lucato, Leandro Tavares
Rosemberg, Sérgio
Filho, Vicente Odone
author_sort Barreto, Juliana Silveira
collection PubMed
description OBJECTIVES: Atypical teratoid/rhabdoid tumor (AT/RT) is a rare, highly malignant tumor of the central nervous system with poor prognosis. Nowadays, multimodal management, including surgery, chemotherapy (CMT), radiation therapy (RT) and Bone Marrow Transplantation (BMT). The aim of this study was to assess the experience and survival in a center of reference of treatment in childhood cancer in Brazil. PATIENTS AND METHODS: Medical records of AT/RT patients who underwent surgery from 2008 to 2020 at a center of childhood cancer treatment (ITACI) in São Paulo University were retrospectively reviewed and statistically analyzed. RESULTS: Eight patients (2 males and 6 females) were presented with AT/RTs. Median age during presentation was 22 months (range, 0 - 6 years). Seven patients (88%) were < 18 months and one patient were >18 months. Tumor location was supratentorial in four patients, infratentorial in 2 patients. Kidney disease as the primary diagnosis in 2 patients (25%). Surgical treatment was performed in 4 patients. Seven children underwent total CMT and 3 children were treated with RT. Only 3 patients underwent Autologous Bone Marrow Transplantation (ABMT). The chemotherapy management protocol of the patients was variable: 2 patients received the EU-RHAB protocol, 2 patients received the HEAD START III protocol, 3 patients received chemotherapy in the ICE regimen (Ifosfamide + Carboplatin + Etoposide) and 1 patient received chemotherapy in the CDDP+CTX+VCR (Cyclophosphamide + Cisplatin + Vincristine) regimen. All patients had episodes of neutropenic fever when they received chemotherapy, requiring hospitalization and use of an antibiotic treatment. Among the 8 patients analyzed, all died. CONCLUSIONS: Despite progress in treatment, AT/RT of the CNS disease or primary kidney disease associated with a lack of standardization in a regimen contributes to the dismal prognosis. There is a high mortality in patients with AT/RT, similar to that found in the literature.
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spelling pubmed-91653132022-06-06 ATRT-06. Atypical Teratoid Rhabdoid Tumors (ATRT): results from a Single Institution in Brazil - São Paulo University Barreto, Juliana Silveira Gomez, Karen Nirit Melo Dutra, Alvaro Pimenta De Azambuja, Alessandra Milani Prandini Cristofani, Lilian Maria Sanders, Felipe Hada Petito, Carlo Baraldi, Helena Espindola Weltman, Eduardo Ferraciolli, Suely Fazio Frassetto, Fernando Pereira Lucato, Leandro Tavares Rosemberg, Sérgio Filho, Vicente Odone Neuro Oncol Atypical Teratoid Rhabdoid Tumor OBJECTIVES: Atypical teratoid/rhabdoid tumor (AT/RT) is a rare, highly malignant tumor of the central nervous system with poor prognosis. Nowadays, multimodal management, including surgery, chemotherapy (CMT), radiation therapy (RT) and Bone Marrow Transplantation (BMT). The aim of this study was to assess the experience and survival in a center of reference of treatment in childhood cancer in Brazil. PATIENTS AND METHODS: Medical records of AT/RT patients who underwent surgery from 2008 to 2020 at a center of childhood cancer treatment (ITACI) in São Paulo University were retrospectively reviewed and statistically analyzed. RESULTS: Eight patients (2 males and 6 females) were presented with AT/RTs. Median age during presentation was 22 months (range, 0 - 6 years). Seven patients (88%) were < 18 months and one patient were >18 months. Tumor location was supratentorial in four patients, infratentorial in 2 patients. Kidney disease as the primary diagnosis in 2 patients (25%). Surgical treatment was performed in 4 patients. Seven children underwent total CMT and 3 children were treated with RT. Only 3 patients underwent Autologous Bone Marrow Transplantation (ABMT). The chemotherapy management protocol of the patients was variable: 2 patients received the EU-RHAB protocol, 2 patients received the HEAD START III protocol, 3 patients received chemotherapy in the ICE regimen (Ifosfamide + Carboplatin + Etoposide) and 1 patient received chemotherapy in the CDDP+CTX+VCR (Cyclophosphamide + Cisplatin + Vincristine) regimen. All patients had episodes of neutropenic fever when they received chemotherapy, requiring hospitalization and use of an antibiotic treatment. Among the 8 patients analyzed, all died. CONCLUSIONS: Despite progress in treatment, AT/RT of the CNS disease or primary kidney disease associated with a lack of standardization in a regimen contributes to the dismal prognosis. There is a high mortality in patients with AT/RT, similar to that found in the literature. Oxford University Press 2022-06-03 /pmc/articles/PMC9165313/ http://dx.doi.org/10.1093/neuonc/noac079.005 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Atypical Teratoid Rhabdoid Tumor
Barreto, Juliana Silveira
Gomez, Karen Nirit Melo
Dutra, Alvaro Pimenta
De Azambuja, Alessandra Milani Prandini
Cristofani, Lilian Maria
Sanders, Felipe Hada
Petito, Carlo
Baraldi, Helena Espindola
Weltman, Eduardo
Ferraciolli, Suely Fazio
Frassetto, Fernando Pereira
Lucato, Leandro Tavares
Rosemberg, Sérgio
Filho, Vicente Odone
ATRT-06. Atypical Teratoid Rhabdoid Tumors (ATRT): results from a Single Institution in Brazil - São Paulo University
title ATRT-06. Atypical Teratoid Rhabdoid Tumors (ATRT): results from a Single Institution in Brazil - São Paulo University
title_full ATRT-06. Atypical Teratoid Rhabdoid Tumors (ATRT): results from a Single Institution in Brazil - São Paulo University
title_fullStr ATRT-06. Atypical Teratoid Rhabdoid Tumors (ATRT): results from a Single Institution in Brazil - São Paulo University
title_full_unstemmed ATRT-06. Atypical Teratoid Rhabdoid Tumors (ATRT): results from a Single Institution in Brazil - São Paulo University
title_short ATRT-06. Atypical Teratoid Rhabdoid Tumors (ATRT): results from a Single Institution in Brazil - São Paulo University
title_sort atrt-06. atypical teratoid rhabdoid tumors (atrt): results from a single institution in brazil - são paulo university
topic Atypical Teratoid Rhabdoid Tumor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9165313/
http://dx.doi.org/10.1093/neuonc/noac079.005
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