Cargando…
Machine learning approaches for imaging‐based prognostication of the outcome of surgery for mesial temporal lobe epilepsy
OBJECTIVES: Around 30% of patients undergoing surgical resection for drug‐resistant mesial temporal lobe epilepsy (MTLE) do not obtain seizure freedom. Success of anterior temporal lobe resection (ATLR) critically depends on the careful selection of surgical candidates, aiming at optimizing seizure...
Autores principales: | , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545680/ https://www.ncbi.nlm.nih.gov/pubmed/35266138 http://dx.doi.org/10.1111/epi.17217 |
_version_ | 1784804873559080960 |
---|---|
author | Sinclair, Benjamin Cahill, Varduhi Seah, Jarrel Kitchen, Andy Vivash, Lucy E. Chen, Zhibin Malpas, Charles B. O'Shea, Marie F. Desmond, Patricia M. Hicks, Rodney J. Morokoff, Andrew P. King, James A. Fabinyi, Gavin C. Kaye, Andrew H. Kwan, Patrick Berkovic, Samuel F. Law, Meng O'Brien, Terence J. |
author_facet | Sinclair, Benjamin Cahill, Varduhi Seah, Jarrel Kitchen, Andy Vivash, Lucy E. Chen, Zhibin Malpas, Charles B. O'Shea, Marie F. Desmond, Patricia M. Hicks, Rodney J. Morokoff, Andrew P. King, James A. Fabinyi, Gavin C. Kaye, Andrew H. Kwan, Patrick Berkovic, Samuel F. Law, Meng O'Brien, Terence J. |
author_sort | Sinclair, Benjamin |
collection | PubMed |
description | OBJECTIVES: Around 30% of patients undergoing surgical resection for drug‐resistant mesial temporal lobe epilepsy (MTLE) do not obtain seizure freedom. Success of anterior temporal lobe resection (ATLR) critically depends on the careful selection of surgical candidates, aiming at optimizing seizure freedom while minimizing postoperative morbidity. Structural MRI and FDG‐PET neuroimaging are routinely used in presurgical assessment and guide the decision to proceed to surgery. In this study, we evaluate the potential of machine learning techniques applied to standard presurgical MRI and PET imaging features to provide enhanced prognostic value relative to current practice. METHODS: Eighty two patients with drug resistant MTLE were scanned with FDG‐PET pre‐surgery and T1‐weighted MRI pre‐ and postsurgery. From these images the following features of interest were derived: volume of temporal lobe (TL) hypometabolism, % of extratemporal hypometabolism, presence of contralateral TL hypometabolism, presence of hippocampal sclerosis, laterality of seizure onset volume of tissue resected and % of temporal lobe hypometabolism resected. These measures were used as predictor variables in logistic regression, support vector machines, random forests and artificial neural networks. RESULTS: In the study cohort, 24 of 82 (28.3%) who underwent an ATLR for drug‐resistant MTLE did not achieve Engel Class I (i.e., free of disabling seizures) outcome at a minimum of 2 years of postoperative follow‐up. We found that machine learning approaches were able to predict up to 73% of the 24 ATLR surgical patients who did not achieve a Class I outcome, at the expense of incorrect prediction for up to 31% of patients who did achieve a Class I outcome. Overall accuracies ranged from 70% to 80%, with an area under the receiver operating characteristic curve (AUC) of .75–.81. We additionally found that information regarding overall extent of both total and significantly hypometabolic tissue resected was crucial to predictive performance, with AUC dropping to .59–.62 using presurgical information alone. Incorporating the laterality of seizure onset and the choice of machine learning algorithm did not significantly change predictive performance. SIGNIFICANCE: Collectively, these results indicate that "acceptable" to "good" patient‐specific prognostication for drug‐resistant MTLE surgery is feasible with machine learning approaches utilizing commonly collected imaging modalities, but that information on the surgical resection region is critical for optimal prognostication. |
format | Online Article Text |
id | pubmed-9545680 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95456802022-10-14 Machine learning approaches for imaging‐based prognostication of the outcome of surgery for mesial temporal lobe epilepsy Sinclair, Benjamin Cahill, Varduhi Seah, Jarrel Kitchen, Andy Vivash, Lucy E. Chen, Zhibin Malpas, Charles B. O'Shea, Marie F. Desmond, Patricia M. Hicks, Rodney J. Morokoff, Andrew P. King, James A. Fabinyi, Gavin C. Kaye, Andrew H. Kwan, Patrick Berkovic, Samuel F. Law, Meng O'Brien, Terence J. Epilepsia Research Article OBJECTIVES: Around 30% of patients undergoing surgical resection for drug‐resistant mesial temporal lobe epilepsy (MTLE) do not obtain seizure freedom. Success of anterior temporal lobe resection (ATLR) critically depends on the careful selection of surgical candidates, aiming at optimizing seizure freedom while minimizing postoperative morbidity. Structural MRI and FDG‐PET neuroimaging are routinely used in presurgical assessment and guide the decision to proceed to surgery. In this study, we evaluate the potential of machine learning techniques applied to standard presurgical MRI and PET imaging features to provide enhanced prognostic value relative to current practice. METHODS: Eighty two patients with drug resistant MTLE were scanned with FDG‐PET pre‐surgery and T1‐weighted MRI pre‐ and postsurgery. From these images the following features of interest were derived: volume of temporal lobe (TL) hypometabolism, % of extratemporal hypometabolism, presence of contralateral TL hypometabolism, presence of hippocampal sclerosis, laterality of seizure onset volume of tissue resected and % of temporal lobe hypometabolism resected. These measures were used as predictor variables in logistic regression, support vector machines, random forests and artificial neural networks. RESULTS: In the study cohort, 24 of 82 (28.3%) who underwent an ATLR for drug‐resistant MTLE did not achieve Engel Class I (i.e., free of disabling seizures) outcome at a minimum of 2 years of postoperative follow‐up. We found that machine learning approaches were able to predict up to 73% of the 24 ATLR surgical patients who did not achieve a Class I outcome, at the expense of incorrect prediction for up to 31% of patients who did achieve a Class I outcome. Overall accuracies ranged from 70% to 80%, with an area under the receiver operating characteristic curve (AUC) of .75–.81. We additionally found that information regarding overall extent of both total and significantly hypometabolic tissue resected was crucial to predictive performance, with AUC dropping to .59–.62 using presurgical information alone. Incorporating the laterality of seizure onset and the choice of machine learning algorithm did not significantly change predictive performance. SIGNIFICANCE: Collectively, these results indicate that "acceptable" to "good" patient‐specific prognostication for drug‐resistant MTLE surgery is feasible with machine learning approaches utilizing commonly collected imaging modalities, but that information on the surgical resection region is critical for optimal prognostication. John Wiley and Sons Inc. 2022-03-25 2022-05 /pmc/articles/PMC9545680/ /pubmed/35266138 http://dx.doi.org/10.1111/epi.17217 Text en © 2022 The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Article Sinclair, Benjamin Cahill, Varduhi Seah, Jarrel Kitchen, Andy Vivash, Lucy E. Chen, Zhibin Malpas, Charles B. O'Shea, Marie F. Desmond, Patricia M. Hicks, Rodney J. Morokoff, Andrew P. King, James A. Fabinyi, Gavin C. Kaye, Andrew H. Kwan, Patrick Berkovic, Samuel F. Law, Meng O'Brien, Terence J. Machine learning approaches for imaging‐based prognostication of the outcome of surgery for mesial temporal lobe epilepsy |
title | Machine learning approaches for imaging‐based prognostication of the outcome of surgery for mesial temporal lobe epilepsy |
title_full | Machine learning approaches for imaging‐based prognostication of the outcome of surgery for mesial temporal lobe epilepsy |
title_fullStr | Machine learning approaches for imaging‐based prognostication of the outcome of surgery for mesial temporal lobe epilepsy |
title_full_unstemmed | Machine learning approaches for imaging‐based prognostication of the outcome of surgery for mesial temporal lobe epilepsy |
title_short | Machine learning approaches for imaging‐based prognostication of the outcome of surgery for mesial temporal lobe epilepsy |
title_sort | machine learning approaches for imaging‐based prognostication of the outcome of surgery for mesial temporal lobe epilepsy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545680/ https://www.ncbi.nlm.nih.gov/pubmed/35266138 http://dx.doi.org/10.1111/epi.17217 |
work_keys_str_mv | AT sinclairbenjamin machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT cahillvarduhi machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT seahjarrel machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT kitchenandy machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT vivashlucye machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT chenzhibin machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT malpascharlesb machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT osheamarief machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT desmondpatriciam machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT hicksrodneyj machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT morokoffandrewp machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT kingjamesa machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT fabinyigavinc machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT kayeandrewh machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT kwanpatrick machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT berkovicsamuelf machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT lawmeng machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy AT obrienterencej machinelearningapproachesforimagingbasedprognosticationoftheoutcomeofsurgeryformesialtemporallobeepilepsy |