Hippocampus-Avoidance Whole-Brain Radiation Therapy Is Efficient in the Long-Term Preservation of Hippocampal Volume.

MRI WBRT (whole-brain radiation therapy) atrophy cognitive function hippocampus

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2021
Historique:
received: 25 05 2021
accepted: 26 07 2021
entrez: 7 9 2021
pubmed: 8 9 2021
medline: 8 9 2021
Statut: epublish

Résumé

With improved life expectancy, preventing neurocognitive decline after cerebral radiotherapy is gaining more importance. Hippocampal damage has been considered the main culprit for cognitive deficits following conventional whole-brain radiation therapy (WBRT). Here, we aimed to determine to which extent hippocampus-avoidance WBRT (HA-WBRT) can prevent hippocampal atrophy compared to conventional WBRT. Thirty-five HA-WBRT and 48 WBRT patients were retrospectively selected, comprising a total of 544 contrast-enhanced T1-weighted magnetic resonance imaging studies, longitudinally acquired within 24 months before and 48 months after radiotherapy. HA-WBRT patients were treated analogously to the ongoing HIPPORAD-trial (DRKS00004598) protocol with 30 Gy in 12 fractions and dose to 98% of the hippocampus ≤ 9 Gy and to 2% ≤ 17 Gy. WBRT was mainly performed with 35 Gy in 14 fractions or 30 Gy in 10 fractions. Anatomical images were segmented and the hippocampal volume was quantified using the Computational Anatomy Toolbox (CAT), including neuroradiological expert review of the segmentations. After statistically controlling for confounding variables such as age, gender, and total intracranial volume, hippocampal atrophy was found after both WBRT and HA-WBRT ( HA-WBRT is a therapeutic option for patients with multiple brain metastases, which can effectively and durably minimize hippocampal atrophy compared to conventional WBRT.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
With improved life expectancy, preventing neurocognitive decline after cerebral radiotherapy is gaining more importance. Hippocampal damage has been considered the main culprit for cognitive deficits following conventional whole-brain radiation therapy (WBRT). Here, we aimed to determine to which extent hippocampus-avoidance WBRT (HA-WBRT) can prevent hippocampal atrophy compared to conventional WBRT.
METHODS AND MATERIALS METHODS
Thirty-five HA-WBRT and 48 WBRT patients were retrospectively selected, comprising a total of 544 contrast-enhanced T1-weighted magnetic resonance imaging studies, longitudinally acquired within 24 months before and 48 months after radiotherapy. HA-WBRT patients were treated analogously to the ongoing HIPPORAD-trial (DRKS00004598) protocol with 30 Gy in 12 fractions and dose to 98% of the hippocampus ≤ 9 Gy and to 2% ≤ 17 Gy. WBRT was mainly performed with 35 Gy in 14 fractions or 30 Gy in 10 fractions. Anatomical images were segmented and the hippocampal volume was quantified using the Computational Anatomy Toolbox (CAT), including neuroradiological expert review of the segmentations.
RESULTS RESULTS
After statistically controlling for confounding variables such as age, gender, and total intracranial volume, hippocampal atrophy was found after both WBRT and HA-WBRT (
CONCLUSION CONCLUSIONS
HA-WBRT is a therapeutic option for patients with multiple brain metastases, which can effectively and durably minimize hippocampal atrophy compared to conventional WBRT.

Identifiants

pubmed: 34490112
doi: 10.3389/fonc.2021.714709
pmc: PMC8417356
doi:

Types de publication

Journal Article

Langues

eng

Pagination

714709

Informations de copyright

Copyright © 2021 Popp, Rau, Kellner, Reisert, Fennell, Rothe, Nieder, Urbach, Egger, Grosu and Kaller.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

Breast Cancer Res Treat. 2012 Apr;132(3):1099-106
pubmed: 22205140
Cancer Res. 2003 Jul 15;63(14):4021-7
pubmed: 12874001
Int J Radiat Oncol Biol Phys. 2017 Jul 1;98(3):603-611
pubmed: 28581401
Med Oncol. 2000 Nov;17(4):279-86
pubmed: 11114706
Int J Radiat Oncol Biol Phys. 2015 Mar 15;91(4):781-6
pubmed: 25752392
Cancer. 2020 Jun 1;126(11):2694-2703
pubmed: 32142171
J Clin Oncol. 2020 Apr 1;38(10):1019-1029
pubmed: 32058845
CNS Neurosci Ther. 2016 Jun;22(6):440-50
pubmed: 26861512
Neuroscience. 2003;119(3):635-42
pubmed: 12809684
Folia Morphol (Warsz). 2021;80(1):26-32
pubmed: 32159839
J Clin Med. 2019 Feb 11;8(2):
pubmed: 30754707
J Clin Oncol. 2004 Jan 1;22(1):157-65
pubmed: 14701778
Cancer Imaging. 2019 Jan 22;19(1):2
pubmed: 30670096
Lancet Oncol. 2009 Nov;10(11):1037-44
pubmed: 19801201
Brain. 2010 Apr;133(Pt 4):1163-72
pubmed: 20375138
JAMA. 2016 Jul 26;316(4):401-409
pubmed: 27458945
Strahlenther Onkol. 2015 Jun;191(6):461-9
pubmed: 25592907
Int J Radiat Oncol Biol Phys. 2012 Jul 15;83(4):e487-93
pubmed: 22209148
Neurotox Res. 2014 May;25(4):369-80
pubmed: 24277158
Cochrane Database Syst Rev. 2018 Jan 25;1:CD003869
pubmed: 29365347
Brain Imaging Behav. 2019 Aug;13(4):1160-1171
pubmed: 30054872
Int J Radiat Oncol Biol Phys. 2008 Dec 1;72(5):1311-8
pubmed: 18448270
Neurology. 2000 Aug 22;55(4):484-89
pubmed: 10953178
Sci Rep. 2017 Sep 15;7(1):11667
pubmed: 28916767
J Neurosci. 2019 Jan 30;39(5):918-928
pubmed: 30587540
J Clin Oncol. 2014 Dec 1;32(34):3810-6
pubmed: 25349290
Cancer. 2004 Jun 1;100(11):2292-9
pubmed: 15160331
J Clin Oncol. 2004 Jun 1;22(11):2233-9
pubmed: 15169812
Springerplus. 2014 Aug 19;3:444
pubmed: 25184110
Radiother Oncol. 2017 Nov;125(2):234-240
pubmed: 29128167
Int J Radiat Oncol Biol Phys. 2004 Apr 1;58(5):1346-52
pubmed: 15050309
Int J Radiat Oncol Biol Phys. 2017 Feb 1;97(2):263-269
pubmed: 28068234
Int J Radiat Oncol Biol Phys. 2019 Nov 15;105(4):773-783
pubmed: 31408667
Int J Radiat Oncol Biol Phys. 2013 Jan 1;85(1):264-70
pubmed: 22516808
Alzheimers Dement. 2020 Jan;16(1):209-218
pubmed: 31914231
Neurosci Biobehav Rev. 2014 Feb;39:34-50
pubmed: 24374381
Neuroimage Clin. 2019;23:101904
pubmed: 31254939
Nat Med. 2019 Apr;25(4):554-560
pubmed: 30911133
Neuroimage. 2013 Jul 1;74:254-65
pubmed: 23415948
J Clin Oncol. 2013 Jan 1;31(1):65-72
pubmed: 23213105
Neuroimage. 2007 Oct 15;38(1):95-113
pubmed: 17761438
Nature. 2018 Mar 15;555(7696):377-381
pubmed: 29513649
Int J Neuropsychopharmacol. 2018 Feb 1;21(2):187-200
pubmed: 29040650
Nat Rev Neurol. 2012 Mar 13;8(4):189-202
pubmed: 22410582
Clin Transl Radiat Oncol. 2020 Nov 15;26:35-41
pubmed: 33294645
BMC Cancer. 2020 Jun 8;20(1):532
pubmed: 32513138
Nat Med. 2002 Sep;8(9):955-62
pubmed: 12161748

Auteurs

Ilinca Popp (I)

Department of Radiation Oncology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Alexander Rau (A)

Department of Neuroradiology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Elias Kellner (E)

Medical Physics, Department of Radiology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Marco Reisert (M)

Medical Physics, Department of Radiology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Jamina Tara Fennell (JT)

Department of Radiation Oncology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Thomas Rothe (T)

Department of Radiation Oncology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Carsten Nieder (C)

Department of Oncology and Palliative Medicine, Nordland Hospital, Bodø, Norway.
Department of Clinical Medicine, Faculty of Health Sciences, University of Tromsø, Tromsø, Norway.

Horst Urbach (H)

Department of Neuroradiology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Karl Egger (K)

Department of Neuroradiology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Anca Ligia Grosu (AL)

Department of Radiation Oncology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
German Cancer Consortium (DKTK), Partner Site Freiburg, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Christoph P Kaller (CP)

Department of Neuroradiology, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Classifications MeSH