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RARE-08. MULTI-INSTITUTIONAL ANALYSIS OF PEDIATRIC RELAPSED/REFRACTORY CENTRAL NERVOUS SYSTEM GERMINOMA

BACKGROUND: Relapsed central nervous system (CNS) germinomas are rare with no universal agreement regarding management. We explore prognostic factors that may impact the treatment of patients with relapsed CNS germinoma. METHODS: An international multi-institutional retrospective study of relapsed/p...

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Autores principales: McGlynn, Mary Claire, Abu-Arja, Mohammad H, Nagabushan, Sumanth, Zaghloul, Mohamed Saad, Elhemaly, Ahmed, Bertrand, Kelsey, Gajjar, Amar, Alias, Hamidah, Cappellano, Andrea, Graham, Richard, Baglivo, Sofia Jares, Bhadri, Vivek, Govender, Dinisha, Abdelbaki, Mohamed S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10260231/
http://dx.doi.org/10.1093/neuonc/noad073.137
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author McGlynn, Mary Claire
Abu-Arja, Mohammad H
Nagabushan, Sumanth
Zaghloul, Mohamed Saad
Elhemaly, Ahmed
Bertrand, Kelsey
Gajjar, Amar
Alias, Hamidah
Cappellano, Andrea
Graham, Richard
Baglivo, Sofia Jares
Bhadri, Vivek
Govender, Dinisha
Abdelbaki, Mohamed S
author_facet McGlynn, Mary Claire
Abu-Arja, Mohammad H
Nagabushan, Sumanth
Zaghloul, Mohamed Saad
Elhemaly, Ahmed
Bertrand, Kelsey
Gajjar, Amar
Alias, Hamidah
Cappellano, Andrea
Graham, Richard
Baglivo, Sofia Jares
Bhadri, Vivek
Govender, Dinisha
Abdelbaki, Mohamed S
author_sort McGlynn, Mary Claire
collection PubMed
description BACKGROUND: Relapsed central nervous system (CNS) germinomas are rare with no universal agreement regarding management. We explore prognostic factors that may impact the treatment of patients with relapsed CNS germinoma. METHODS: An international multi-institutional retrospective study of relapsed/progressive CNS germinomas was conducted. Data was summarized using descriptive statistics. Overall survival (OS) was evaluated using Kaplan-Meier and Fischer’s exact test to estimate odds ratios (OR) and 95% confidence intervals (CI). RESULTS: Analysis included 21 patients (Male 71.4%) with relapsed/progressive germinomas from 7 sites. Median age at diagnosis was 15 years (interquartile range (IQR): 9.9-19) with 5% presenting with metastatic disease. Twelve patients (57.1%) achieved complete remission (CR) after initial therapy. Nineteen children (90.5%) suffered relapse. One (4.8%) suffered progression. The median time from diagnosis to relapse/progression was 21 months (range: 10-56 months) with 90.5% occurring within 24 months. 19 (90.5%) underwent chemotherapy, 9 (42.9%) bone marrow ablative therapy (HDCx), and 13 (61.9%) radiotherapy. At last follow-up, 88.9% of HDCx and 92.3% of radiotherapy recipients were alive. Of patients receiving radiation, 45% received whole ventricular irradiation, 25% craniospinal irradiation, and 5% focal irradiation (remainder unreported). Eleven children (52.4%) achieved CR after relapse/progression therapy and 16 (76.2%) were alive at last follow-up. Median time to last follow-up was 39 months (IQR: 18.43–89.50). Re-irradiation at relapse (OR=16, 95% CI: 1.27-200.9) and achieving complete response (CR) at relapse/progression (OR=4, 95% CI: 1.04-1.78) were associated with improved OS. CR after initial therapy (OR=0.857, 95%CI: 0.11-6.62) and HDCx at relapse/progression (OR=4, 95%CI: 0.36-44.13) were not associated with improved OS. CONCLUSIONS: Relapsed CNS germinomas are radiosensitive and salvageable by re-irradiation at relapse. This ongoing multi-institutional study will contribute to existing knowledge about relapsed/progressive CNS germinomas and inform prospective clinical trials to improve outcomes for children with relapsed/progressive disease.
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spelling pubmed-102602312023-06-13 RARE-08. MULTI-INSTITUTIONAL ANALYSIS OF PEDIATRIC RELAPSED/REFRACTORY CENTRAL NERVOUS SYSTEM GERMINOMA McGlynn, Mary Claire Abu-Arja, Mohammad H Nagabushan, Sumanth Zaghloul, Mohamed Saad Elhemaly, Ahmed Bertrand, Kelsey Gajjar, Amar Alias, Hamidah Cappellano, Andrea Graham, Richard Baglivo, Sofia Jares Bhadri, Vivek Govender, Dinisha Abdelbaki, Mohamed S Neuro Oncol Final Category: Germ Cell Tumors/Rare Tumors - RARE BACKGROUND: Relapsed central nervous system (CNS) germinomas are rare with no universal agreement regarding management. We explore prognostic factors that may impact the treatment of patients with relapsed CNS germinoma. METHODS: An international multi-institutional retrospective study of relapsed/progressive CNS germinomas was conducted. Data was summarized using descriptive statistics. Overall survival (OS) was evaluated using Kaplan-Meier and Fischer’s exact test to estimate odds ratios (OR) and 95% confidence intervals (CI). RESULTS: Analysis included 21 patients (Male 71.4%) with relapsed/progressive germinomas from 7 sites. Median age at diagnosis was 15 years (interquartile range (IQR): 9.9-19) with 5% presenting with metastatic disease. Twelve patients (57.1%) achieved complete remission (CR) after initial therapy. Nineteen children (90.5%) suffered relapse. One (4.8%) suffered progression. The median time from diagnosis to relapse/progression was 21 months (range: 10-56 months) with 90.5% occurring within 24 months. 19 (90.5%) underwent chemotherapy, 9 (42.9%) bone marrow ablative therapy (HDCx), and 13 (61.9%) radiotherapy. At last follow-up, 88.9% of HDCx and 92.3% of radiotherapy recipients were alive. Of patients receiving radiation, 45% received whole ventricular irradiation, 25% craniospinal irradiation, and 5% focal irradiation (remainder unreported). Eleven children (52.4%) achieved CR after relapse/progression therapy and 16 (76.2%) were alive at last follow-up. Median time to last follow-up was 39 months (IQR: 18.43–89.50). Re-irradiation at relapse (OR=16, 95% CI: 1.27-200.9) and achieving complete response (CR) at relapse/progression (OR=4, 95% CI: 1.04-1.78) were associated with improved OS. CR after initial therapy (OR=0.857, 95%CI: 0.11-6.62) and HDCx at relapse/progression (OR=4, 95%CI: 0.36-44.13) were not associated with improved OS. CONCLUSIONS: Relapsed CNS germinomas are radiosensitive and salvageable by re-irradiation at relapse. This ongoing multi-institutional study will contribute to existing knowledge about relapsed/progressive CNS germinomas and inform prospective clinical trials to improve outcomes for children with relapsed/progressive disease. Oxford University Press 2023-06-12 /pmc/articles/PMC10260231/ http://dx.doi.org/10.1093/neuonc/noad073.137 Text en © The Author(s) 2023. 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 Final Category: Germ Cell Tumors/Rare Tumors - RARE
McGlynn, Mary Claire
Abu-Arja, Mohammad H
Nagabushan, Sumanth
Zaghloul, Mohamed Saad
Elhemaly, Ahmed
Bertrand, Kelsey
Gajjar, Amar
Alias, Hamidah
Cappellano, Andrea
Graham, Richard
Baglivo, Sofia Jares
Bhadri, Vivek
Govender, Dinisha
Abdelbaki, Mohamed S
RARE-08. MULTI-INSTITUTIONAL ANALYSIS OF PEDIATRIC RELAPSED/REFRACTORY CENTRAL NERVOUS SYSTEM GERMINOMA
title RARE-08. MULTI-INSTITUTIONAL ANALYSIS OF PEDIATRIC RELAPSED/REFRACTORY CENTRAL NERVOUS SYSTEM GERMINOMA
title_full RARE-08. MULTI-INSTITUTIONAL ANALYSIS OF PEDIATRIC RELAPSED/REFRACTORY CENTRAL NERVOUS SYSTEM GERMINOMA
title_fullStr RARE-08. MULTI-INSTITUTIONAL ANALYSIS OF PEDIATRIC RELAPSED/REFRACTORY CENTRAL NERVOUS SYSTEM GERMINOMA
title_full_unstemmed RARE-08. MULTI-INSTITUTIONAL ANALYSIS OF PEDIATRIC RELAPSED/REFRACTORY CENTRAL NERVOUS SYSTEM GERMINOMA
title_short RARE-08. MULTI-INSTITUTIONAL ANALYSIS OF PEDIATRIC RELAPSED/REFRACTORY CENTRAL NERVOUS SYSTEM GERMINOMA
title_sort rare-08. multi-institutional analysis of pediatric relapsed/refractory central nervous system germinoma
topic Final Category: Germ Cell Tumors/Rare Tumors - RARE
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10260231/
http://dx.doi.org/10.1093/neuonc/noad073.137
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