{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,22]],"date-time":"2026-10-22T20:17:32Z","timestamp":1792700252700,"version":"4.5.0"},"reference-count":63,"publisher":"American Medical Association (AMA)","issue":"7","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi230639-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Serum creatinine\u2013based estimated glomerular filtration rate (eGFRcr) may overestimate the glomerular filtration rate (GFR) in patients with cancer. Cystatin C\u2013based eGFR (eGFRcys) is an alternative marker of GFR.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi230639-5\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To determine whether the therapeutic drug levels and adverse events (AEs) associated with renally cleared medications were higher in patients with cancer whose eGFRcys was more than 30% lower than their eGFRcr.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi230639-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>This cohort study analyzed adult patients with cancer at 2 major academic cancer centers in Boston, Massachusetts. These patients had their creatinine and cystatin C measured on the same day between May 2010 and January 2022. The date of the first simultaneous eGFRcr and eGFRcys measurement was considered to be the baseline date.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi230639-7\">\n                    <jats:title>Exposure<\/jats:title>\n                    <jats:p>The primary exposure was eGFR discordance, defined as an eGFRcys that was more than 30% lower than the eGFRcr.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi230639-8\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>The primary outcome was risk of the following medication-related AEs within 90 days of the baseline date: (1) supratherapeutic vancomycin trough level greater than 30 \u03bcg\/mL, (2) trimethoprim-sulfamethoxazole\u2013related hyperkalemia (&amp;amp;gt;5.5 mEq\/L), (3) baclofen toxic effect, and (4) supratherapeutic digoxin level (&amp;amp;gt;2.0 ng\/mL). For the secondary outcome, a multivariable Cox proportional hazards regression model was used to compare 30-day survival of those with vs without eGFR discordance.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi230639-9\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      A total of 1869 adult patients with cancer (mean [SD] age, 66 [14] years; 948 males [51%]) had simultaneous eGFRcys and eGFRcr measurement. There were 543 patients (29%) with an eGFRcys that was more than 30% lower than their eGFRcr. Patients with an eGFRcys that was more than 30% lower than their eGFRcr were more likely to experience medication-related AEs compared with patients with concordant eGFRs (defined as eGFRcys within 30% of eGFRcr), including vancomycin levels greater than 30 \u03bcg\/mL (43 of 179 [24%] vs 7 of 77 [9%];\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.01), trimethoprim-sulfamethoxazole\u2013related hyperkalemia (29 of 129 [22%] vs 11 of 92 [12%];\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.07), baclofen toxic effects (5 of 19 [26%] vs 0 of 11;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.19), and supratherapeutic digoxin levels (7 of 24 [29%] vs 0 of 10;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.08). The adjusted odds ratio for vancomycin levels more than 30 \u03bcg\/mL was 2.59 (95% CI, 1.08-7.03;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.04). Patients with an eGFRcys more than 30% lower than their eGFRcr had an increased 30-day mortality (adjusted hazard ratio, 1.98; 95% CI, 1.26-3.11;\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u2009.003).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi230639-10\">\n                    <jats:title>Conclusions and relevance<\/jats:title>\n                    <jats:p>Results of this study suggest that among patients with cancer with simultaneous assessment of eGFRcys and eGFRcr, supratherapeutic drug levels and medication-related AEs occurred more commonly in those with an eGFRcys more than 30% lower than their eGFRcr. Future prospective studies are needed to improve and personalize GFR estimation and medication dosing in patients with cancer.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2023.21715","type":"journal-article","created":{"date-parts":[[2023,7,5]],"date-time":"2023-07-05T11:03:43Z","timestamp":1688555023000},"page":"e2321715","source":"Crossref","is-referenced-by-count":39,"title":["Medication-Related Adverse Events and Discordancies in Cystatin C\u2013Based vs Serum Creatinine\u2013Based Estimated Glomerular Filtration Rate in Patients With Cancer"],"prefix":"10.1001","volume":"6","author":[{"given":"Paul E.","family":"Hanna","sequence":"first","affiliation":[{"name":"Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Qiyu","family":"Wang","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Department of Medicine, Massachusetts General 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Boston"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nurit","family":"Katz-Agranov","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Harish","family":"Seethapathy","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kerry L.","family":"Reynolds","sequence":"additional","affiliation":[{"name":"Division of Hematology and Oncology, Department of Medicine, Massachusetts General Hospital, Boston"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shruti","family":"Gupta","sequence":"additional","affiliation":[{"name":"Division of Renal Medicine, Brigham and Women's Hospital, Boston, Massachusetts"},{"name":"Adult Survivorship Program, Dana-Farber Cancer Institute, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David E.","family":"Leaf","sequence":"additional","affiliation":[{"name":"Division of Renal Medicine, Brigham and Women's Hospital, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Meghan E.","family":"Sise","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"10","published-online":{"date-parts":[[2023,7,5]]},"reference":[{"issue":"3","key":"zoi230639r1","doi-asserted-by":"publisher","first-page":"411","DOI":"10.1053\/j.ajkd.2014.04.010","article-title":"Measuring GFR: a systematic review.","volume":"64","author":"Soveri","year":"2014","journal-title":"Am J Kidney Dis"},{"issue":"6","key":"zoi230639r2","doi-asserted-by":"publisher","first-page":"461","DOI":"10.7326\/0003-4819-130-6-199903160-00002","article-title":"A 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