Glomerular filtration rate estimation for carboplatin dosing in patients with gynaecological cancers

Carboplatin remains integral for treatment of gynaecological malignancies and dosing is based on glomerular filtration rate (GFR). Measurement via radiotracer decay [nuclear medicine GFR (nmGFR)] is ideal. However, this may be unavailable. Therefore GFR is often estimated using formulae that have no...

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Veröffentlicht in:ESMO open 2022-04, Vol.7 (2), p.100401, Article 100401
Hauptverfasser: Samani, A., Bennett, R., Eremeishvili, K., Kalofonou, F., Whear, S., Montes, A., Kristeleit, R., Krell, J., McNeish, I., Ghosh, S., Tookman, L.
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container_start_page 100401
container_title ESMO open
container_volume 7
creator Samani, A.
Bennett, R.
Eremeishvili, K.
Kalofonou, F.
Whear, S.
Montes, A.
Kristeleit, R.
Krell, J.
McNeish, I.
Ghosh, S.
Tookman, L.
description Carboplatin remains integral for treatment of gynaecological malignancies and dosing is based on glomerular filtration rate (GFR). Measurement via radiotracer decay [nuclear medicine GFR (nmGFR)] is ideal. However, this may be unavailable. Therefore GFR is often estimated using formulae that have not been validated in patients with cancer and/or specifically for gynaecological malignancies, leading to debate over optimal estimation. Suboptimal GFR estimation may affect efficacy or toxicity. We surveyed several UK National Health Service Trusts to assess carboplatin dosing practise. We then explored single-centre accuracy, bias and precision of various formulae for GFR estimation, relative to nmGFR, before validating our findings in an external cohort. Across 18 Trusts, there was considerable heterogeneity in GFR estimation, including the formulae used [Cockcroft–Gault (CG) versus Wright], weight adjustment and area under the curve (AUC; 5 versus 6). We analysed 274 and 192 patients in two centres. Overall, CamGFR v2 (a novel formula for GFR estimation developed at Cambridge University Hospitals NHS Foundation Trust) excelled, showing the highest accuracy and precision. This translated into accuracy of hypothetical carboplatin dosing; nmGFR-derived carboplatin dose fell within 20% of the Cam GFR v2-derived dose in 86.5% and 87% of patients across the cohorts. Among the CG formula and its derivatives, using adjusted body weight in those with body mass index ≥25 kg/m2 [CG-adjusted body weight (CG-AdBW)] was optimal. The Wright and unadjusted CG estimators performed most poorly. When compared with nmGFR assessment, accuracy, bias and precision varied widely between GFR estimators, with the newly developed Cam GFR v2 and CG-AdBW performing best. In general, weight (or body surface area)-adjusted formulae excelled, while the unadjusted CG and Wright formulae or the use of AUC6 (versus nmGFR AUC5) produced risk of significant overdose. Thus, individual centres should validate their GFR estimation methods. In the absence of validation, CG-AdBW or CamGFR v2 is likely to perform well while unadjusted CG/Wright formulae or AUC6 dosing should be avoided. •Despite therapeutic advances, carboplatin is still used repeatedly for treatment of gynaecological cancers.•Between centres, there is heterogenous use of GFR estimation methods for carboplatin dosing.•The novel CamGFR v2 and CG-AdBW are the most accurate estimators.•The Wright formula, unadjusted CG and the use of AU
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Measurement via radiotracer decay [nuclear medicine GFR (nmGFR)] is ideal. However, this may be unavailable. Therefore GFR is often estimated using formulae that have not been validated in patients with cancer and/or specifically for gynaecological malignancies, leading to debate over optimal estimation. Suboptimal GFR estimation may affect efficacy or toxicity. We surveyed several UK National Health Service Trusts to assess carboplatin dosing practise. We then explored single-centre accuracy, bias and precision of various formulae for GFR estimation, relative to nmGFR, before validating our findings in an external cohort. Across 18 Trusts, there was considerable heterogeneity in GFR estimation, including the formulae used [Cockcroft–Gault (CG) versus Wright], weight adjustment and area under the curve (AUC; 5 versus 6). We analysed 274 and 192 patients in two centres. Overall, CamGFR v2 (a novel formula for GFR estimation developed at Cambridge University Hospitals NHS Foundation Trust) excelled, showing the highest accuracy and precision. This translated into accuracy of hypothetical carboplatin dosing; nmGFR-derived carboplatin dose fell within 20% of the Cam GFR v2-derived dose in 86.5% and 87% of patients across the cohorts. Among the CG formula and its derivatives, using adjusted body weight in those with body mass index ≥25 kg/m2 [CG-adjusted body weight (CG-AdBW)] was optimal. The Wright and unadjusted CG estimators performed most poorly. When compared with nmGFR assessment, accuracy, bias and precision varied widely between GFR estimators, with the newly developed Cam GFR v2 and CG-AdBW performing best. In general, weight (or body surface area)-adjusted formulae excelled, while the unadjusted CG and Wright formulae or the use of AUC6 (versus nmGFR AUC5) produced risk of significant overdose. 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All rights reserved.</rights><rights>Crown Copyright © 2022 Published by Elsevier Ltd on behalf of European Society for Medical Oncology. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-26cb6ddac2e1027c1a9306e235207a5df10b0432aa8864446a1c9458237b58fe3</citedby><cites>FETCH-LOGICAL-c463t-26cb6ddac2e1027c1a9306e235207a5df10b0432aa8864446a1c9458237b58fe3</cites><orcidid>0000-0003-0752-3974</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9058909/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9058909/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35227967$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Samani, A.</creatorcontrib><creatorcontrib>Bennett, R.</creatorcontrib><creatorcontrib>Eremeishvili, K.</creatorcontrib><creatorcontrib>Kalofonou, F.</creatorcontrib><creatorcontrib>Whear, S.</creatorcontrib><creatorcontrib>Montes, A.</creatorcontrib><creatorcontrib>Kristeleit, R.</creatorcontrib><creatorcontrib>Krell, J.</creatorcontrib><creatorcontrib>McNeish, I.</creatorcontrib><creatorcontrib>Ghosh, S.</creatorcontrib><creatorcontrib>Tookman, L.</creatorcontrib><title>Glomerular filtration rate estimation for carboplatin dosing in patients with gynaecological cancers</title><title>ESMO open</title><addtitle>ESMO Open</addtitle><description>Carboplatin remains integral for treatment of gynaecological malignancies and dosing is based on glomerular filtration rate (GFR). Measurement via radiotracer decay [nuclear medicine GFR (nmGFR)] is ideal. However, this may be unavailable. Therefore GFR is often estimated using formulae that have not been validated in patients with cancer and/or specifically for gynaecological malignancies, leading to debate over optimal estimation. Suboptimal GFR estimation may affect efficacy or toxicity. We surveyed several UK National Health Service Trusts to assess carboplatin dosing practise. We then explored single-centre accuracy, bias and precision of various formulae for GFR estimation, relative to nmGFR, before validating our findings in an external cohort. Across 18 Trusts, there was considerable heterogeneity in GFR estimation, including the formulae used [Cockcroft–Gault (CG) versus Wright], weight adjustment and area under the curve (AUC; 5 versus 6). We analysed 274 and 192 patients in two centres. Overall, CamGFR v2 (a novel formula for GFR estimation developed at Cambridge University Hospitals NHS Foundation Trust) excelled, showing the highest accuracy and precision. This translated into accuracy of hypothetical carboplatin dosing; nmGFR-derived carboplatin dose fell within 20% of the Cam GFR v2-derived dose in 86.5% and 87% of patients across the cohorts. Among the CG formula and its derivatives, using adjusted body weight in those with body mass index ≥25 kg/m2 [CG-adjusted body weight (CG-AdBW)] was optimal. The Wright and unadjusted CG estimators performed most poorly. When compared with nmGFR assessment, accuracy, bias and precision varied widely between GFR estimators, with the newly developed Cam GFR v2 and CG-AdBW performing best. In general, weight (or body surface area)-adjusted formulae excelled, while the unadjusted CG and Wright formulae or the use of AUC6 (versus nmGFR AUC5) produced risk of significant overdose. 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In the absence of validation, CG-AdBW or CamGFR v2 is likely to perform well while unadjusted CG/Wright formulae or AUC6 dosing should be avoided. •Despite therapeutic advances, carboplatin is still used repeatedly for treatment of gynaecological cancers.•Between centres, there is heterogenous use of GFR estimation methods for carboplatin dosing.•The novel CamGFR v2 and CG-AdBW are the most accurate estimators.•The Wright formula, unadjusted CG and the use of AUC6 with estimated GFR should all be avoided.•If internal validation unavailable, centres should use CamGFR v2 or CG-AdBW for GFR estimation.</description><subject>Antineoplastic Agents - adverse effects</subject><subject>Body Weight</subject><subject>carboplatin</subject><subject>Carboplatin - pharmacology</subject><subject>Carboplatin - therapeutic use</subject><subject>chemotherapy</subject><subject>Female</subject><subject>Genital Neoplasms, Female - drug therapy</subject><subject>Glomerular Filtration Rate</subject><subject>gynaecological cancers</subject><subject>Humans</subject><subject>Original Research</subject><subject>Retrospective Studies</subject><subject>State Medicine</subject><subject>toxicity</subject><issn>2059-7029</issn><issn>2059-7029</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UEFOwzAQtBCIVqU_QCgfaFk7jpNckFAFBakSFzhbjrNJXaVxZKdF_T2uAqVcOO3urGZ2dgi5pTCnQMX9Zo5-a203Z8BYgIADvSBjBkk-S4Hll2f9iEy93wAATXkAxTUZxQljaS7SMSmXjd2i2zXKRZVpeqd6Y9soFIzQ92Y7zJV1kVausF0TgDYqrTdtHYWuCzO2vY8-Tb-O6kOrUNvG1karJlBajc7fkKtKNR6n33VCPp6f3hcvs9Xb8nXxuJppLuJ-xoQuRFkqzZACSzVVeQwCWXALqUrKikIBPGZKZZngnAtFdc6TjMVpkWQVxhPyMOh2u2KLpQ6-nGpk58Ib7iCtMvLvpjVrWdu9zCHJcsiDAB8EtLPeO6xOXAryGLzcyCF4eQxeDsEH2t353RPpJ-ZfYxi-3xt00uuQmsbSONS9LK35_8IX1RqZSQ</recordid><startdate>20220401</startdate><enddate>20220401</enddate><creator>Samani, A.</creator><creator>Bennett, R.</creator><creator>Eremeishvili, K.</creator><creator>Kalofonou, F.</creator><creator>Whear, S.</creator><creator>Montes, A.</creator><creator>Kristeleit, R.</creator><creator>Krell, J.</creator><creator>McNeish, I.</creator><creator>Ghosh, S.</creator><creator>Tookman, L.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0752-3974</orcidid></search><sort><creationdate>20220401</creationdate><title>Glomerular filtration rate estimation for carboplatin dosing in patients with gynaecological cancers</title><author>Samani, A. ; Bennett, R. ; Eremeishvili, K. ; Kalofonou, F. ; Whear, S. ; Montes, A. ; Kristeleit, R. ; Krell, J. ; McNeish, I. ; Ghosh, S. ; Tookman, L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-26cb6ddac2e1027c1a9306e235207a5df10b0432aa8864446a1c9458237b58fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antineoplastic Agents - adverse effects</topic><topic>Body Weight</topic><topic>carboplatin</topic><topic>Carboplatin - pharmacology</topic><topic>Carboplatin - therapeutic use</topic><topic>chemotherapy</topic><topic>Female</topic><topic>Genital Neoplasms, Female - drug therapy</topic><topic>Glomerular Filtration Rate</topic><topic>gynaecological cancers</topic><topic>Humans</topic><topic>Original Research</topic><topic>Retrospective Studies</topic><topic>State Medicine</topic><topic>toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Samani, A.</creatorcontrib><creatorcontrib>Bennett, R.</creatorcontrib><creatorcontrib>Eremeishvili, K.</creatorcontrib><creatorcontrib>Kalofonou, F.</creatorcontrib><creatorcontrib>Whear, S.</creatorcontrib><creatorcontrib>Montes, A.</creatorcontrib><creatorcontrib>Kristeleit, R.</creatorcontrib><creatorcontrib>Krell, J.</creatorcontrib><creatorcontrib>McNeish, I.</creatorcontrib><creatorcontrib>Ghosh, S.</creatorcontrib><creatorcontrib>Tookman, L.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>ESMO open</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Samani, A.</au><au>Bennett, R.</au><au>Eremeishvili, K.</au><au>Kalofonou, F.</au><au>Whear, S.</au><au>Montes, A.</au><au>Kristeleit, R.</au><au>Krell, J.</au><au>McNeish, I.</au><au>Ghosh, S.</au><au>Tookman, L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glomerular filtration rate estimation for carboplatin dosing in patients with gynaecological cancers</atitle><jtitle>ESMO open</jtitle><addtitle>ESMO Open</addtitle><date>2022-04-01</date><risdate>2022</risdate><volume>7</volume><issue>2</issue><spage>100401</spage><pages>100401-</pages><artnum>100401</artnum><issn>2059-7029</issn><eissn>2059-7029</eissn><abstract>Carboplatin remains integral for treatment of gynaecological malignancies and dosing is based on glomerular filtration rate (GFR). Measurement via radiotracer decay [nuclear medicine GFR (nmGFR)] is ideal. However, this may be unavailable. Therefore GFR is often estimated using formulae that have not been validated in patients with cancer and/or specifically for gynaecological malignancies, leading to debate over optimal estimation. Suboptimal GFR estimation may affect efficacy or toxicity. We surveyed several UK National Health Service Trusts to assess carboplatin dosing practise. We then explored single-centre accuracy, bias and precision of various formulae for GFR estimation, relative to nmGFR, before validating our findings in an external cohort. Across 18 Trusts, there was considerable heterogeneity in GFR estimation, including the formulae used [Cockcroft–Gault (CG) versus Wright], weight adjustment and area under the curve (AUC; 5 versus 6). We analysed 274 and 192 patients in two centres. Overall, CamGFR v2 (a novel formula for GFR estimation developed at Cambridge University Hospitals NHS Foundation Trust) excelled, showing the highest accuracy and precision. This translated into accuracy of hypothetical carboplatin dosing; nmGFR-derived carboplatin dose fell within 20% of the Cam GFR v2-derived dose in 86.5% and 87% of patients across the cohorts. Among the CG formula and its derivatives, using adjusted body weight in those with body mass index ≥25 kg/m2 [CG-adjusted body weight (CG-AdBW)] was optimal. The Wright and unadjusted CG estimators performed most poorly. When compared with nmGFR assessment, accuracy, bias and precision varied widely between GFR estimators, with the newly developed Cam GFR v2 and CG-AdBW performing best. In general, weight (or body surface area)-adjusted formulae excelled, while the unadjusted CG and Wright formulae or the use of AUC6 (versus nmGFR AUC5) produced risk of significant overdose. Thus, individual centres should validate their GFR estimation methods. In the absence of validation, CG-AdBW or CamGFR v2 is likely to perform well while unadjusted CG/Wright formulae or AUC6 dosing should be avoided. •Despite therapeutic advances, carboplatin is still used repeatedly for treatment of gynaecological cancers.•Between centres, there is heterogenous use of GFR estimation methods for carboplatin dosing.•The novel CamGFR v2 and CG-AdBW are the most accurate estimators.•The Wright formula, unadjusted CG and the use of AUC6 with estimated GFR should all be avoided.•If internal validation unavailable, centres should use CamGFR v2 or CG-AdBW for GFR estimation.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>35227967</pmid><doi>10.1016/j.esmoop.2022.100401</doi><orcidid>https://orcid.org/0000-0003-0752-3974</orcidid><oa>free_for_read</oa></addata></record>
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subjects Antineoplastic Agents - adverse effects
Body Weight
carboplatin
Carboplatin - pharmacology
Carboplatin - therapeutic use
chemotherapy
Female
Genital Neoplasms, Female - drug therapy
Glomerular Filtration Rate
gynaecological cancers
Humans
Original Research
Retrospective Studies
State Medicine
toxicity
title Glomerular filtration rate estimation for carboplatin dosing in patients with gynaecological cancers
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