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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
Main Authors: 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
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container_issue Supplement_1
container_start_page i33
container_title Neuro-oncology advances
container_volume 6
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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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. 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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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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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