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RMTD-02 PRACTICE VARIATION AND IMPACT OF PRE-OPERATIVE AND POST-OPERATIVE DEXAMETHASONE ON PATIENT OUTCOME IN THE RESECTED BRAIN METASTASIS – INSIGHTS FROM THE CLINDEXMET MULTICENTER REGISTRY
Abstract BACKGROUND Patients with brain metastases that undergo brain metastasis resection regularly receive perioperative dexamethasone. We sought to evaluate variation in pre- and post-operative dexamethasone dosing and whether perioperative dexamethasone in brain metastases is linked to patient o...
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Published in: | Neuro-oncology advances 2024-08, Vol.6 (Supplement_1), p.i33-i33 |
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creator | Wasilewski, David Tommaso, Araceli Rafaelian, Artem Demetz, Matthias Asey, Benedikt Ersoy, Tunc-Faik Dauth, Alice Peukert, Ricarda Poeser, Paul Jelgersma, Claudius Früh, Anton Xu, Ran Capper, David Ehret, Felix Frost, Nikolaj Schmidt, Leon Krenzlin, Harald Ringel, Florian Meyer, Hanno Gempt, Jens Kerschbaumer, Johannes Freyschlag, Christian Thomé, Claudius Simon, Matthias Dubinski, Daniel Freiman, Thomas Schmidt, Nils Ole Proescholdt, Martin Vajkoczy, Peter Onken, Julia |
description | Abstract
BACKGROUND
Patients with brain metastases that undergo brain metastasis resection regularly receive perioperative dexamethasone. We sought to evaluate variation in pre- and post-operative dexamethasone dosing and whether perioperative dexamethasone in brain metastases is linked to patient outcome.
METHODS
This was a multicenter retrospective study collecting data on daily pre- and post-operative dexamethasone dosage over a period of 27 days in patients undergoing brain metastasis resection. Non arbitrary cutpoint selection was performed using maximally selected rank statistics to dichotomize patients. Propensity score matching served to reduce bias and adjust for potential confounders including tumor and edema volume, localization of the dominant brain metastasis, disease-specifc GPA score, presence of other non-oncological diseases.
RESULTS
988 patients were included. Median follow-up time was 55,2 months [95% CI: 50.7 – 61.5]. After propensity score matching patients below the determined cutpoint of 122 mg cumulative dexamethasone showed an overall survival of 16.0 months [95% CI: 13.3 – 21] vs. patients with more than 122 mg cumulative dexamethasone with a OS of 10.6 months [9.0 – 12.7], p=0.0022. No effect on extracranial or intracranial disease progression was observed. In a multivariable model for the matched data the cumulative peri-operative dexamethasone above the cutpoint remained independently associated with overall survival (HR: 1.3 [95% CI: 1.12 – 1.6], p=0.001).
CONCLUSION
Cumulative perioperative dexamethasone is associated with decreased survival in the context of brain metastasis resection. Strict dosage, down taper or methods reducing corticosteroid dependency should be regularly evaluated in clinical practice in patients with brain metastases. |
doi_str_mv | 10.1093/noajnl/vdae090.109 |
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BACKGROUND
Patients with brain metastases that undergo brain metastasis resection regularly receive perioperative dexamethasone. We sought to evaluate variation in pre- and post-operative dexamethasone dosing and whether perioperative dexamethasone in brain metastases is linked to patient outcome.
METHODS
This was a multicenter retrospective study collecting data on daily pre- and post-operative dexamethasone dosage over a period of 27 days in patients undergoing brain metastasis resection. Non arbitrary cutpoint selection was performed using maximally selected rank statistics to dichotomize patients. Propensity score matching served to reduce bias and adjust for potential confounders including tumor and edema volume, localization of the dominant brain metastasis, disease-specifc GPA score, presence of other non-oncological diseases.
RESULTS
988 patients were included. Median follow-up time was 55,2 months [95% CI: 50.7 – 61.5]. After propensity score matching patients below the determined cutpoint of 122 mg cumulative dexamethasone showed an overall survival of 16.0 months [95% CI: 13.3 – 21] vs. patients with more than 122 mg cumulative dexamethasone with a OS of 10.6 months [9.0 – 12.7], p=0.0022. No effect on extracranial or intracranial disease progression was observed. In a multivariable model for the matched data the cumulative peri-operative dexamethasone above the cutpoint remained independently associated with overall survival (HR: 1.3 [95% CI: 1.12 – 1.6], p=0.001).
CONCLUSION
Cumulative perioperative dexamethasone is associated with decreased survival in the context of brain metastasis resection. Strict dosage, down taper or methods reducing corticosteroid dependency should be regularly evaluated in clinical practice in patients with brain metastases.</description><identifier>ISSN: 2632-2498</identifier><identifier>EISSN: 2632-2498</identifier><identifier>DOI: 10.1093/noajnl/vdae090.109</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Final Category: Research Methods and Trial Design Considerations</subject><ispartof>Neuro-oncology advances, 2024-08, Vol.6 (Supplement_1), p.i33-i33</ispartof><rights>The Author(s) 2024. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11296740/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11296740/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids></links><search><creatorcontrib>Wasilewski, David</creatorcontrib><creatorcontrib>Tommaso, Araceli</creatorcontrib><creatorcontrib>Rafaelian, Artem</creatorcontrib><creatorcontrib>Demetz, Matthias</creatorcontrib><creatorcontrib>Asey, Benedikt</creatorcontrib><creatorcontrib>Ersoy, Tunc-Faik</creatorcontrib><creatorcontrib>Dauth, Alice</creatorcontrib><creatorcontrib>Peukert, Ricarda</creatorcontrib><creatorcontrib>Poeser, Paul</creatorcontrib><creatorcontrib>Jelgersma, Claudius</creatorcontrib><creatorcontrib>Früh, Anton</creatorcontrib><creatorcontrib>Xu, Ran</creatorcontrib><creatorcontrib>Capper, David</creatorcontrib><creatorcontrib>Ehret, Felix</creatorcontrib><creatorcontrib>Frost, Nikolaj</creatorcontrib><creatorcontrib>Schmidt, Leon</creatorcontrib><creatorcontrib>Krenzlin, Harald</creatorcontrib><creatorcontrib>Ringel, Florian</creatorcontrib><creatorcontrib>Meyer, Hanno</creatorcontrib><creatorcontrib>Gempt, Jens</creatorcontrib><creatorcontrib>Kerschbaumer, Johannes</creatorcontrib><creatorcontrib>Freyschlag, Christian</creatorcontrib><creatorcontrib>Thomé, Claudius</creatorcontrib><creatorcontrib>Simon, Matthias</creatorcontrib><creatorcontrib>Dubinski, Daniel</creatorcontrib><creatorcontrib>Freiman, Thomas</creatorcontrib><creatorcontrib>Schmidt, Nils Ole</creatorcontrib><creatorcontrib>Proescholdt, Martin</creatorcontrib><creatorcontrib>Vajkoczy, Peter</creatorcontrib><creatorcontrib>Onken, Julia</creatorcontrib><title>RMTD-02 PRACTICE VARIATION AND IMPACT OF PRE-OPERATIVE AND POST-OPERATIVE DEXAMETHASONE ON PATIENT OUTCOME IN THE RESECTED BRAIN METASTASIS – INSIGHTS FROM THE CLINDEXMET MULTICENTER REGISTRY</title><title>Neuro-oncology advances</title><description>Abstract
BACKGROUND
Patients with brain metastases that undergo brain metastasis resection regularly receive perioperative dexamethasone. We sought to evaluate variation in pre- and post-operative dexamethasone dosing and whether perioperative dexamethasone in brain metastases is linked to patient outcome.
METHODS
This was a multicenter retrospective study collecting data on daily pre- and post-operative dexamethasone dosage over a period of 27 days in patients undergoing brain metastasis resection. Non arbitrary cutpoint selection was performed using maximally selected rank statistics to dichotomize patients. Propensity score matching served to reduce bias and adjust for potential confounders including tumor and edema volume, localization of the dominant brain metastasis, disease-specifc GPA score, presence of other non-oncological diseases.
RESULTS
988 patients were included. Median follow-up time was 55,2 months [95% CI: 50.7 – 61.5]. After propensity score matching patients below the determined cutpoint of 122 mg cumulative dexamethasone showed an overall survival of 16.0 months [95% CI: 13.3 – 21] vs. patients with more than 122 mg cumulative dexamethasone with a OS of 10.6 months [9.0 – 12.7], p=0.0022. No effect on extracranial or intracranial disease progression was observed. In a multivariable model for the matched data the cumulative peri-operative dexamethasone above the cutpoint remained independently associated with overall survival (HR: 1.3 [95% CI: 1.12 – 1.6], p=0.001).
CONCLUSION
Cumulative perioperative dexamethasone is associated with decreased survival in the context of brain metastasis resection. Strict dosage, down taper or methods reducing corticosteroid dependency should be regularly evaluated in clinical practice in patients with brain metastases.</description><subject>Final Category: Research Methods and Trial Design Considerations</subject><issn>2632-2498</issn><issn>2632-2498</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNqNkdtKwzAYx4MoKNMX8CovUE3Sw9YriV22BdYDaSZ6VbI11clcR-sG3vkOPpGv4pP47YDonSSQ8PsfSPgQuqTkipLQvV7W5nm5uN6UxpJwx47QGQtc5jAv7B3_up-ii7Z9JoQw3_M9ws7Qp4p13yEMZ4pHWkYC33EluZZpgnnSxzLOgON0AAbhpJlQoN2JnZaluf6F-uKex0KPeJ4mAkM-Ay4SCE90lMYCywTrkcBK5CLSoo9vFQcEEZ7Dljn-ev8AUy6HI53jgUrjnT8aywS6wYfjyXj7xkQLBTVDmWv1cI5OKrNo7cXh7KDJQOho5IzToYz42JnRHg0d-HHAfMv8Ken5ge9aa32PVSbskdBjvktKQ2FVMxpYUnWDMqi6tAwtsWwaBl3jdtDNvne1nr7YcmaXr41ZFKtm_mKat6I28-Kvspw_FY_1pqCUQYFHoIHtG2ZN3baNrX7ClBTbSRb7SRaHSe5YBzn7UL1e_cf_DTBJl5Y</recordid><startdate>20240802</startdate><enddate>20240802</enddate><creator>Wasilewski, David</creator><creator>Tommaso, Araceli</creator><creator>Rafaelian, Artem</creator><creator>Demetz, Matthias</creator><creator>Asey, Benedikt</creator><creator>Ersoy, Tunc-Faik</creator><creator>Dauth, Alice</creator><creator>Peukert, Ricarda</creator><creator>Poeser, Paul</creator><creator>Jelgersma, Claudius</creator><creator>Früh, Anton</creator><creator>Xu, Ran</creator><creator>Capper, David</creator><creator>Ehret, Felix</creator><creator>Frost, Nikolaj</creator><creator>Schmidt, Leon</creator><creator>Krenzlin, Harald</creator><creator>Ringel, Florian</creator><creator>Meyer, Hanno</creator><creator>Gempt, Jens</creator><creator>Kerschbaumer, Johannes</creator><creator>Freyschlag, Christian</creator><creator>Thomé, Claudius</creator><creator>Simon, Matthias</creator><creator>Dubinski, Daniel</creator><creator>Freiman, Thomas</creator><creator>Schmidt, Nils Ole</creator><creator>Proescholdt, Martin</creator><creator>Vajkoczy, Peter</creator><creator>Onken, Julia</creator><general>Oxford University Press</general><scope>TOX</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20240802</creationdate><title>RMTD-02 PRACTICE VARIATION AND IMPACT OF PRE-OPERATIVE AND POST-OPERATIVE DEXAMETHASONE ON PATIENT OUTCOME IN THE RESECTED BRAIN METASTASIS – INSIGHTS FROM THE CLINDEXMET MULTICENTER REGISTRY</title><author>Wasilewski, David ; Tommaso, Araceli ; Rafaelian, Artem ; Demetz, Matthias ; Asey, Benedikt ; Ersoy, Tunc-Faik ; Dauth, Alice ; Peukert, Ricarda ; Poeser, Paul ; Jelgersma, Claudius ; Früh, Anton ; Xu, Ran ; Capper, David ; Ehret, Felix ; Frost, Nikolaj ; Schmidt, Leon ; Krenzlin, Harald ; Ringel, Florian ; Meyer, Hanno ; Gempt, Jens ; Kerschbaumer, Johannes ; Freyschlag, Christian ; Thomé, Claudius ; Simon, Matthias ; Dubinski, Daniel ; Freiman, Thomas ; Schmidt, Nils Ole ; Proescholdt, Martin ; Vajkoczy, Peter ; Onken, Julia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1819-254625e25b085653eee542fa980942530da1a1afc16e0f76d6f71d9e0e2b967a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Final Category: Research Methods and Trial Design Considerations</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wasilewski, David</creatorcontrib><creatorcontrib>Tommaso, Araceli</creatorcontrib><creatorcontrib>Rafaelian, Artem</creatorcontrib><creatorcontrib>Demetz, Matthias</creatorcontrib><creatorcontrib>Asey, Benedikt</creatorcontrib><creatorcontrib>Ersoy, Tunc-Faik</creatorcontrib><creatorcontrib>Dauth, Alice</creatorcontrib><creatorcontrib>Peukert, Ricarda</creatorcontrib><creatorcontrib>Poeser, Paul</creatorcontrib><creatorcontrib>Jelgersma, Claudius</creatorcontrib><creatorcontrib>Früh, Anton</creatorcontrib><creatorcontrib>Xu, Ran</creatorcontrib><creatorcontrib>Capper, David</creatorcontrib><creatorcontrib>Ehret, Felix</creatorcontrib><creatorcontrib>Frost, Nikolaj</creatorcontrib><creatorcontrib>Schmidt, Leon</creatorcontrib><creatorcontrib>Krenzlin, Harald</creatorcontrib><creatorcontrib>Ringel, Florian</creatorcontrib><creatorcontrib>Meyer, Hanno</creatorcontrib><creatorcontrib>Gempt, Jens</creatorcontrib><creatorcontrib>Kerschbaumer, Johannes</creatorcontrib><creatorcontrib>Freyschlag, Christian</creatorcontrib><creatorcontrib>Thomé, Claudius</creatorcontrib><creatorcontrib>Simon, Matthias</creatorcontrib><creatorcontrib>Dubinski, Daniel</creatorcontrib><creatorcontrib>Freiman, Thomas</creatorcontrib><creatorcontrib>Schmidt, Nils Ole</creatorcontrib><creatorcontrib>Proescholdt, Martin</creatorcontrib><creatorcontrib>Vajkoczy, Peter</creatorcontrib><creatorcontrib>Onken, Julia</creatorcontrib><collection>Oxford University Press Open Access</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neuro-oncology advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wasilewski, David</au><au>Tommaso, Araceli</au><au>Rafaelian, Artem</au><au>Demetz, Matthias</au><au>Asey, Benedikt</au><au>Ersoy, Tunc-Faik</au><au>Dauth, Alice</au><au>Peukert, Ricarda</au><au>Poeser, Paul</au><au>Jelgersma, Claudius</au><au>Früh, Anton</au><au>Xu, Ran</au><au>Capper, David</au><au>Ehret, Felix</au><au>Frost, Nikolaj</au><au>Schmidt, Leon</au><au>Krenzlin, Harald</au><au>Ringel, Florian</au><au>Meyer, Hanno</au><au>Gempt, Jens</au><au>Kerschbaumer, Johannes</au><au>Freyschlag, Christian</au><au>Thomé, Claudius</au><au>Simon, Matthias</au><au>Dubinski, Daniel</au><au>Freiman, Thomas</au><au>Schmidt, Nils Ole</au><au>Proescholdt, Martin</au><au>Vajkoczy, Peter</au><au>Onken, Julia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>RMTD-02 PRACTICE VARIATION AND IMPACT OF PRE-OPERATIVE AND POST-OPERATIVE DEXAMETHASONE ON PATIENT OUTCOME IN THE RESECTED BRAIN METASTASIS – INSIGHTS FROM THE CLINDEXMET MULTICENTER REGISTRY</atitle><jtitle>Neuro-oncology advances</jtitle><date>2024-08-02</date><risdate>2024</risdate><volume>6</volume><issue>Supplement_1</issue><spage>i33</spage><epage>i33</epage><pages>i33-i33</pages><issn>2632-2498</issn><eissn>2632-2498</eissn><abstract>Abstract
BACKGROUND
Patients with brain metastases that undergo brain metastasis resection regularly receive perioperative dexamethasone. We sought to evaluate variation in pre- and post-operative dexamethasone dosing and whether perioperative dexamethasone in brain metastases is linked to patient outcome.
METHODS
This was a multicenter retrospective study collecting data on daily pre- and post-operative dexamethasone dosage over a period of 27 days in patients undergoing brain metastasis resection. Non arbitrary cutpoint selection was performed using maximally selected rank statistics to dichotomize patients. Propensity score matching served to reduce bias and adjust for potential confounders including tumor and edema volume, localization of the dominant brain metastasis, disease-specifc GPA score, presence of other non-oncological diseases.
RESULTS
988 patients were included. Median follow-up time was 55,2 months [95% CI: 50.7 – 61.5]. After propensity score matching patients below the determined cutpoint of 122 mg cumulative dexamethasone showed an overall survival of 16.0 months [95% CI: 13.3 – 21] vs. patients with more than 122 mg cumulative dexamethasone with a OS of 10.6 months [9.0 – 12.7], p=0.0022. No effect on extracranial or intracranial disease progression was observed. In a multivariable model for the matched data the cumulative peri-operative dexamethasone above the cutpoint remained independently associated with overall survival (HR: 1.3 [95% CI: 1.12 – 1.6], p=0.001).
CONCLUSION
Cumulative perioperative dexamethasone is associated with decreased survival in the context of brain metastasis resection. Strict dosage, down taper or methods reducing corticosteroid dependency should be regularly evaluated in clinical practice in patients with brain metastases.</abstract><cop>US</cop><pub>Oxford University Press</pub><doi>10.1093/noajnl/vdae090.109</doi><oa>free_for_read</oa></addata></record> |
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subjects | Final Category: Research Methods and Trial Design Considerations |
title | RMTD-02 PRACTICE VARIATION AND IMPACT OF PRE-OPERATIVE AND POST-OPERATIVE DEXAMETHASONE ON PATIENT OUTCOME IN THE RESECTED BRAIN METASTASIS – INSIGHTS FROM THE CLINDEXMET MULTICENTER REGISTRY |
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