Cargando…

OTHR-03. Brain Metastasis Among Ovarian Cancer Patients

BACKGROUND: Brain metastasis (BM) are uncommon among ovarian cancer (OC) patients. Their frequency, risk factors and clinical repercussions are not well described. We assessed OC patients who developed BM, the role of BRCA status and survival implications. METHODS: Study cohort included OC patients...

Descripción completa

Detalles Bibliográficos
Autores principales: Limon, Dror, Shachar, Eliya, Adar, Lyri, Hasson, Shira Peleg, Safra, Tamar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351262/
http://dx.doi.org/10.1093/noajnl/vdab071.058
_version_ 1783735936748617728
author Limon, Dror
Shachar, Eliya
Adar, Lyri
Hasson, Shira Peleg
Safra, Tamar
author_facet Limon, Dror
Shachar, Eliya
Adar, Lyri
Hasson, Shira Peleg
Safra, Tamar
author_sort Limon, Dror
collection PubMed
description BACKGROUND: Brain metastasis (BM) are uncommon among ovarian cancer (OC) patients. Their frequency, risk factors and clinical repercussions are not well described. We assessed OC patients who developed BM, the role of BRCA status and survival implications. METHODS: Study cohort included OC patients treated at our center, from 2002–2020. We retrospectively evaluated clinical parameters, risk for BM development and association with survival data. RESULTS: Among 972 OC patients, 28 (2.9%) were diagnosed with BM. Comparing the BM to non-BM group, median age of 60 across both groups, stage III-IV at diagnosis was more common among BM group (96.4% vs. 84.8%, p=0.0065) while platinum sensitivity was similar (92.3% in BM vs. 80.8% in non-BM, p=0.2193). Out of 658 patients tested for BRCA, 33.6% (n=221) were BRCA mutation carriers (BRCA+). Of the patients with BM, 22 tested for BRCA, 13 were carriers. BRCA+ was significantly higher in the BM group compared to the non-BM group (59.1% vs. 32.9%, p=0.0123). Among BRCA+ the rate of BM was higher than among BRCA- (5.8% vs. 2.1%, p=0.0123, HR=3.029; 95%CI: 1.4–6.5). Median time from OC diagnosis to BM and from disease recurrence to BM, was longer for BRCA+ compared to BRCA- (44.3mo vs. 32.3mo and 11.8mo vs. 0.7mo, respectively). Median survival (mOS) was not significantly different among patients with BM compared to those without BM (59.4mo vs. 71.2mo, p=0.36). Following diagnosis of BM, mOS was 20.6mo among BRCA+ and 12.3mo among BRCA- (p=0.4266). No correlation was demonstrated with PARP inhibitors or bevacizumab treatment and subsequent development of BM. CONCLUSION: BM are an infrequent event among OC patients. However, the risk is three-folds higher among BRCA+. Interestingly, BM do not significantly alter survival among OC patients. Our work suggests that the higher rate of BM in BRCA+ may be related to longer survival. Another hypothesis requiring further evaluation, is possible higher brain tropism among this population.
format Online
Article
Text
id pubmed-8351262
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-83512622021-08-09 OTHR-03. Brain Metastasis Among Ovarian Cancer Patients Limon, Dror Shachar, Eliya Adar, Lyri Hasson, Shira Peleg Safra, Tamar Neurooncol Adv Supplement Abstracts BACKGROUND: Brain metastasis (BM) are uncommon among ovarian cancer (OC) patients. Their frequency, risk factors and clinical repercussions are not well described. We assessed OC patients who developed BM, the role of BRCA status and survival implications. METHODS: Study cohort included OC patients treated at our center, from 2002–2020. We retrospectively evaluated clinical parameters, risk for BM development and association with survival data. RESULTS: Among 972 OC patients, 28 (2.9%) were diagnosed with BM. Comparing the BM to non-BM group, median age of 60 across both groups, stage III-IV at diagnosis was more common among BM group (96.4% vs. 84.8%, p=0.0065) while platinum sensitivity was similar (92.3% in BM vs. 80.8% in non-BM, p=0.2193). Out of 658 patients tested for BRCA, 33.6% (n=221) were BRCA mutation carriers (BRCA+). Of the patients with BM, 22 tested for BRCA, 13 were carriers. BRCA+ was significantly higher in the BM group compared to the non-BM group (59.1% vs. 32.9%, p=0.0123). Among BRCA+ the rate of BM was higher than among BRCA- (5.8% vs. 2.1%, p=0.0123, HR=3.029; 95%CI: 1.4–6.5). Median time from OC diagnosis to BM and from disease recurrence to BM, was longer for BRCA+ compared to BRCA- (44.3mo vs. 32.3mo and 11.8mo vs. 0.7mo, respectively). Median survival (mOS) was not significantly different among patients with BM compared to those without BM (59.4mo vs. 71.2mo, p=0.36). Following diagnosis of BM, mOS was 20.6mo among BRCA+ and 12.3mo among BRCA- (p=0.4266). No correlation was demonstrated with PARP inhibitors or bevacizumab treatment and subsequent development of BM. CONCLUSION: BM are an infrequent event among OC patients. However, the risk is three-folds higher among BRCA+. Interestingly, BM do not significantly alter survival among OC patients. Our work suggests that the higher rate of BM in BRCA+ may be related to longer survival. Another hypothesis requiring further evaluation, is possible higher brain tropism among this population. Oxford University Press 2021-08-09 /pmc/articles/PMC8351262/ http://dx.doi.org/10.1093/noajnl/vdab071.058 Text en © The Author(s) 2021. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of 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 (http://creativecommons.org/licenses/by-nc/4.0/ (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 Supplement Abstracts
Limon, Dror
Shachar, Eliya
Adar, Lyri
Hasson, Shira Peleg
Safra, Tamar
OTHR-03. Brain Metastasis Among Ovarian Cancer Patients
title OTHR-03. Brain Metastasis Among Ovarian Cancer Patients
title_full OTHR-03. Brain Metastasis Among Ovarian Cancer Patients
title_fullStr OTHR-03. Brain Metastasis Among Ovarian Cancer Patients
title_full_unstemmed OTHR-03. Brain Metastasis Among Ovarian Cancer Patients
title_short OTHR-03. Brain Metastasis Among Ovarian Cancer Patients
title_sort othr-03. brain metastasis among ovarian cancer patients
topic Supplement Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351262/
http://dx.doi.org/10.1093/noajnl/vdab071.058
work_keys_str_mv AT limondror othr03brainmetastasisamongovariancancerpatients
AT shachareliya othr03brainmetastasisamongovariancancerpatients
AT adarlyri othr03brainmetastasisamongovariancancerpatients
AT hassonshirapeleg othr03brainmetastasisamongovariancancerpatients
AT safratamar othr03brainmetastasisamongovariancancerpatients