Cargando…

RARE-15. EARLY PSEUDOPROGRESSION POST-RADIATION IN PAEDIATRIC HIGH-GRADE GLIOMA PATIENTS WITH CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY: TWO CASE REPORTS FROM A SINGLE CENTRE

BACKGROUND: Constitutional Mismatch Repair Deficiency (CMMRD) is a cancer predisposition syndrome caused by biallelic mutations in the mismatch repair pathway, and high-grade glioma (HGG) constitute the most prevalent brain tumours. Pseudoprogression alludes to radiological changes that mimic tumour...

Descripción completa

Detalles Bibliográficos
Autores principales: Teng, Ay-Jiuan, Gilmartin, Breege, Campbell, Marty, Bhatia, Kanika, Wheeler, Greg, Sullivan, Michael, Hansford, Jordan, Khuong-Quang, Dong-Anh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715264/
http://dx.doi.org/10.1093/neuonc/noaa222.726
_version_ 1783618914543992832
author Teng, Ay-Jiuan
Gilmartin, Breege
Campbell, Marty
Bhatia, Kanika
Wheeler, Greg
Sullivan, Michael
Hansford, Jordan
Khuong-Quang, Dong-Anh
author_facet Teng, Ay-Jiuan
Gilmartin, Breege
Campbell, Marty
Bhatia, Kanika
Wheeler, Greg
Sullivan, Michael
Hansford, Jordan
Khuong-Quang, Dong-Anh
author_sort Teng, Ay-Jiuan
collection PubMed
description BACKGROUND: Constitutional Mismatch Repair Deficiency (CMMRD) is a cancer predisposition syndrome caused by biallelic mutations in the mismatch repair pathway, and high-grade glioma (HGG) constitute the most prevalent brain tumours. Pseudoprogression alludes to radiological changes that mimic tumour progression, but are in fact due to other causes such as therapy related inflammation. It can occur as early as three months post treatment. To our knowledge, its characteristics in CMMRD patients has not been reported. METHODS: We retrospectively identified seven patients with CMMRD and history of HGG at The Royal Children’s Hospital, Melbourne from 2005 to 2019. Our objective was to review the characteristics of pseudoprogression in this cohort. RESULTS: Out of the seven patients, two with constitutional loss of PMS2 demonstrated evidence of pseudoprogression. Patient 1 presented at 16 years old with a cerebellar anaplastic astrocytoma. She developed clinical and radiological progression within two weeks of starting radiotherapy, persisting up to four months after completion. However, six months post radiation she improved without intervention and the tumour remains stable five years post therapy. Patient 2 presented at 17 years old with a midbrain anaplastic astrocytoma, and showed signs of progression four weeks after completion of radiotherapy. She was then treated with Bevacizumab, an anti-VEGFA antibody with remarkable response. She subsequently received Nivolumab, a checkpoint inhibitor with ongoing stable disease for four months. CONCLUSION: Our findings showed that pseudoprogression can occur early in the treatment course in CMMRD patients. Identification of this entity is important for appropriate clinical management.
format Online
Article
Text
id pubmed-7715264
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-77152642020-12-09 RARE-15. EARLY PSEUDOPROGRESSION POST-RADIATION IN PAEDIATRIC HIGH-GRADE GLIOMA PATIENTS WITH CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY: TWO CASE REPORTS FROM A SINGLE CENTRE Teng, Ay-Jiuan Gilmartin, Breege Campbell, Marty Bhatia, Kanika Wheeler, Greg Sullivan, Michael Hansford, Jordan Khuong-Quang, Dong-Anh Neuro Oncol Craniopharyngioma and Rare Tumors BACKGROUND: Constitutional Mismatch Repair Deficiency (CMMRD) is a cancer predisposition syndrome caused by biallelic mutations in the mismatch repair pathway, and high-grade glioma (HGG) constitute the most prevalent brain tumours. Pseudoprogression alludes to radiological changes that mimic tumour progression, but are in fact due to other causes such as therapy related inflammation. It can occur as early as three months post treatment. To our knowledge, its characteristics in CMMRD patients has not been reported. METHODS: We retrospectively identified seven patients with CMMRD and history of HGG at The Royal Children’s Hospital, Melbourne from 2005 to 2019. Our objective was to review the characteristics of pseudoprogression in this cohort. RESULTS: Out of the seven patients, two with constitutional loss of PMS2 demonstrated evidence of pseudoprogression. Patient 1 presented at 16 years old with a cerebellar anaplastic astrocytoma. She developed clinical and radiological progression within two weeks of starting radiotherapy, persisting up to four months after completion. However, six months post radiation she improved without intervention and the tumour remains stable five years post therapy. Patient 2 presented at 17 years old with a midbrain anaplastic astrocytoma, and showed signs of progression four weeks after completion of radiotherapy. She was then treated with Bevacizumab, an anti-VEGFA antibody with remarkable response. She subsequently received Nivolumab, a checkpoint inhibitor with ongoing stable disease for four months. CONCLUSION: Our findings showed that pseudoprogression can occur early in the treatment course in CMMRD patients. Identification of this entity is important for appropriate clinical management. Oxford University Press 2020-12-04 /pmc/articles/PMC7715264/ http://dx.doi.org/10.1093/neuonc/noaa222.726 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://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 Craniopharyngioma and Rare Tumors
Teng, Ay-Jiuan
Gilmartin, Breege
Campbell, Marty
Bhatia, Kanika
Wheeler, Greg
Sullivan, Michael
Hansford, Jordan
Khuong-Quang, Dong-Anh
RARE-15. EARLY PSEUDOPROGRESSION POST-RADIATION IN PAEDIATRIC HIGH-GRADE GLIOMA PATIENTS WITH CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY: TWO CASE REPORTS FROM A SINGLE CENTRE
title RARE-15. EARLY PSEUDOPROGRESSION POST-RADIATION IN PAEDIATRIC HIGH-GRADE GLIOMA PATIENTS WITH CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY: TWO CASE REPORTS FROM A SINGLE CENTRE
title_full RARE-15. EARLY PSEUDOPROGRESSION POST-RADIATION IN PAEDIATRIC HIGH-GRADE GLIOMA PATIENTS WITH CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY: TWO CASE REPORTS FROM A SINGLE CENTRE
title_fullStr RARE-15. EARLY PSEUDOPROGRESSION POST-RADIATION IN PAEDIATRIC HIGH-GRADE GLIOMA PATIENTS WITH CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY: TWO CASE REPORTS FROM A SINGLE CENTRE
title_full_unstemmed RARE-15. EARLY PSEUDOPROGRESSION POST-RADIATION IN PAEDIATRIC HIGH-GRADE GLIOMA PATIENTS WITH CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY: TWO CASE REPORTS FROM A SINGLE CENTRE
title_short RARE-15. EARLY PSEUDOPROGRESSION POST-RADIATION IN PAEDIATRIC HIGH-GRADE GLIOMA PATIENTS WITH CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY: TWO CASE REPORTS FROM A SINGLE CENTRE
title_sort rare-15. early pseudoprogression post-radiation in paediatric high-grade glioma patients with constitutional mismatch repair deficiency: two case reports from a single centre
topic Craniopharyngioma and Rare Tumors
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7715264/
http://dx.doi.org/10.1093/neuonc/noaa222.726
work_keys_str_mv AT tengayjiuan rare15earlypseudoprogressionpostradiationinpaediatrichighgradegliomapatientswithconstitutionalmismatchrepairdeficiencytwocasereportsfromasinglecentre
AT gilmartinbreege rare15earlypseudoprogressionpostradiationinpaediatrichighgradegliomapatientswithconstitutionalmismatchrepairdeficiencytwocasereportsfromasinglecentre
AT campbellmarty rare15earlypseudoprogressionpostradiationinpaediatrichighgradegliomapatientswithconstitutionalmismatchrepairdeficiencytwocasereportsfromasinglecentre
AT bhatiakanika rare15earlypseudoprogressionpostradiationinpaediatrichighgradegliomapatientswithconstitutionalmismatchrepairdeficiencytwocasereportsfromasinglecentre
AT wheelergreg rare15earlypseudoprogressionpostradiationinpaediatrichighgradegliomapatientswithconstitutionalmismatchrepairdeficiencytwocasereportsfromasinglecentre
AT sullivanmichael rare15earlypseudoprogressionpostradiationinpaediatrichighgradegliomapatientswithconstitutionalmismatchrepairdeficiencytwocasereportsfromasinglecentre
AT hansfordjordan rare15earlypseudoprogressionpostradiationinpaediatrichighgradegliomapatientswithconstitutionalmismatchrepairdeficiencytwocasereportsfromasinglecentre
AT khuongquangdonganh rare15earlypseudoprogressionpostradiationinpaediatrichighgradegliomapatientswithconstitutionalmismatchrepairdeficiencytwocasereportsfromasinglecentre