Loading…

Renal function evaluation in patients with cancer who were scheduled to receive carboplatin or S-1

Background Accurate glomerular filtration rate (GFR) evaluation is significant for drug dosing of carboplatin, anticancer drug excreted mainly from kidney. Serum cystatin-C (sCys-C) is a GFR marker with little affected by body muscle mass volume. And GFR equations based on serum creatinine (eGFRcrea...

Full description

Saved in:
Bibliographic Details
Published in:Clinical and experimental nephrology 2015-12, Vol.19 (6), p.1107-1113
Main Authors: Shibata, Kanako, Yasuda, Yoshinari, Kobayashi, Ryo, Ando, Yuichi, Shimokata, Tomoya, Kamiya, Hideki, Hayashi, Mutsuharu, Maruyama, Shoichi, Matsuo, Seiichi, Nakao, Makoto, Tsuchiya, Teruo, Teramachi, Hitomi
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c521t-ec537baa989745b598bd35f8df0667af7f796f6c8af7635c031437d0d62f2e0b3
cites cdi_FETCH-LOGICAL-c521t-ec537baa989745b598bd35f8df0667af7f796f6c8af7635c031437d0d62f2e0b3
container_end_page 1113
container_issue 6
container_start_page 1107
container_title Clinical and experimental nephrology
container_volume 19
creator Shibata, Kanako
Yasuda, Yoshinari
Kobayashi, Ryo
Ando, Yuichi
Shimokata, Tomoya
Kamiya, Hideki
Hayashi, Mutsuharu
Maruyama, Shoichi
Matsuo, Seiichi
Nakao, Makoto
Tsuchiya, Teruo
Teramachi, Hitomi
description Background Accurate glomerular filtration rate (GFR) evaluation is significant for drug dosing of carboplatin, anticancer drug excreted mainly from kidney. Serum cystatin-C (sCys-C) is a GFR marker with little affected by body muscle mass volume. And GFR equations based on serum creatinine (eGFRcreat) and sCys-C (eGFRcys) were developed; however, accuracy of eGFRcys has not been elucidated fully among patients with cancer. Therefore, we analyzed the performance of GFR equations among patients with cancer whose GFR values were measured by inulin clearance (Cin). Methods Study design was a cross-sectional study. Subjects were 41 patients with cancer whose GFR values were measured by Cin for drug dosing studies of carboplatin or S-1 in Nagoya University Hospital from 2007 to 2010 and 29 non-cancer patients. Correlation with Cin and slope of regression line were evaluated in eGFRcreat and eGFRcys. Single and multiple regression analyses were analyzed to identify associating factors with eGFRcreat/Cin or eGFRcys/Cin. Results Age, body weight, body mass index (BMI) and sCr were different between cancer patients and non-cancer patients, but sCys-C and Cin were consistent in 2 groups. The slope of the regression line for Cin vs. eGFRcys with zero intercept in cancer patients was 1.10 (95 % CI: 1.02–1.17), which was significantly different from 1.0. In multiple regression analysis revealed that BMI and urinary creatinine excretion were significantly associated with eGFRcreat/Cin, and cancer was only associating factor with eGFRcys/Cin. Conclusion eGFRcys should not be used for evaluation of renal function in patients with cancer because it underestimates GFR.
doi_str_mv 10.1007/s10157-015-1115-1
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1749991656</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1749991656</sourcerecordid><originalsourceid>FETCH-LOGICAL-c521t-ec537baa989745b598bd35f8df0667af7f796f6c8af7635c031437d0d62f2e0b3</originalsourceid><addsrcrecordid>eNp1kUtLxDAUhYMozvj4AW4k4MZNNUmbplmK-AJB8LEOaXrjVDrJmLQz-O9NZ1REcHNyIN-5IfcgdETJGSVEnEdKKBdZkozSUbbQlBa5yISQcjv5vGAZFZxO0F6Mb4SQSnK5iyaMV7JgjExR_QhOd9gOzvStdxiWuhv02rYOL5ID10e8avsZNtoZCHg183gFAXA0M2iGDhrcexzAQLuEBIXaL7oUdNgH_JTRA7RjdRfh8OvcRy_XV8-Xt9n9w83d5cV9ZjijfQaG56LWWlZSFLzmsqqbnNuqsaQshbbCClna0lTJljk3JB-_2pCmZJYBqfN9dLqZuwj-fYDYq3kbDXSdduCHqKgopJS05GVCT_6gb34IaRFrqkoUy0eKbigTfIwBrFqEdq7Dh6JEjQWoTQEqiRoLUDRljr8mD_Ucmp_E98YTwDZATFfuFcKvp_-d-glFzJAT</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1748991236</pqid></control><display><type>article</type><title>Renal function evaluation in patients with cancer who were scheduled to receive carboplatin or S-1</title><source>Springer Link</source><creator>Shibata, Kanako ; Yasuda, Yoshinari ; Kobayashi, Ryo ; Ando, Yuichi ; Shimokata, Tomoya ; Kamiya, Hideki ; Hayashi, Mutsuharu ; Maruyama, Shoichi ; Matsuo, Seiichi ; Nakao, Makoto ; Tsuchiya, Teruo ; Teramachi, Hitomi</creator><creatorcontrib>Shibata, Kanako ; Yasuda, Yoshinari ; Kobayashi, Ryo ; Ando, Yuichi ; Shimokata, Tomoya ; Kamiya, Hideki ; Hayashi, Mutsuharu ; Maruyama, Shoichi ; Matsuo, Seiichi ; Nakao, Makoto ; Tsuchiya, Teruo ; Teramachi, Hitomi</creatorcontrib><description>Background Accurate glomerular filtration rate (GFR) evaluation is significant for drug dosing of carboplatin, anticancer drug excreted mainly from kidney. Serum cystatin-C (sCys-C) is a GFR marker with little affected by body muscle mass volume. And GFR equations based on serum creatinine (eGFRcreat) and sCys-C (eGFRcys) were developed; however, accuracy of eGFRcys has not been elucidated fully among patients with cancer. Therefore, we analyzed the performance of GFR equations among patients with cancer whose GFR values were measured by inulin clearance (Cin). Methods Study design was a cross-sectional study. Subjects were 41 patients with cancer whose GFR values were measured by Cin for drug dosing studies of carboplatin or S-1 in Nagoya University Hospital from 2007 to 2010 and 29 non-cancer patients. Correlation with Cin and slope of regression line were evaluated in eGFRcreat and eGFRcys. Single and multiple regression analyses were analyzed to identify associating factors with eGFRcreat/Cin or eGFRcys/Cin. Results Age, body weight, body mass index (BMI) and sCr were different between cancer patients and non-cancer patients, but sCys-C and Cin were consistent in 2 groups. The slope of the regression line for Cin vs. eGFRcys with zero intercept in cancer patients was 1.10 (95 % CI: 1.02–1.17), which was significantly different from 1.0. In multiple regression analysis revealed that BMI and urinary creatinine excretion were significantly associated with eGFRcreat/Cin, and cancer was only associating factor with eGFRcys/Cin. Conclusion eGFRcys should not be used for evaluation of renal function in patients with cancer because it underestimates GFR.</description><identifier>ISSN: 1342-1751</identifier><identifier>EISSN: 1437-7799</identifier><identifier>DOI: 10.1007/s10157-015-1115-1</identifier><identifier>PMID: 25894220</identifier><identifier>CODEN: CENPFV</identifier><language>eng</language><publisher>Tokyo: Springer Japan</publisher><subject>Aged ; Antineoplastic Agents - adverse effects ; Antineoplastic Agents - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Body Mass Index ; Carboplatin - adverse effects ; Carboplatin - therapeutic use ; Creatinine - blood ; Cross-Sectional Studies ; Cystatin C - blood ; Drug Combinations ; Female ; Glomerular Filtration Rate ; Humans ; Inulin - metabolism ; Kidney Function Tests - methods ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Neoplasms - drug therapy ; Neoplasms - physiopathology ; Nephrology ; Original Article ; Oxonic Acid - adverse effects ; Oxonic Acid - therapeutic use ; Pyridines - adverse effects ; Pyridines - therapeutic use ; Tegafur - adverse effects ; Tegafur - therapeutic use ; Urology</subject><ispartof>Clinical and experimental nephrology, 2015-12, Vol.19 (6), p.1107-1113</ispartof><rights>Japanese Society of Nephrology 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-ec537baa989745b598bd35f8df0667af7f796f6c8af7635c031437d0d62f2e0b3</citedby><cites>FETCH-LOGICAL-c521t-ec537baa989745b598bd35f8df0667af7f796f6c8af7635c031437d0d62f2e0b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25894220$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shibata, Kanako</creatorcontrib><creatorcontrib>Yasuda, Yoshinari</creatorcontrib><creatorcontrib>Kobayashi, Ryo</creatorcontrib><creatorcontrib>Ando, Yuichi</creatorcontrib><creatorcontrib>Shimokata, Tomoya</creatorcontrib><creatorcontrib>Kamiya, Hideki</creatorcontrib><creatorcontrib>Hayashi, Mutsuharu</creatorcontrib><creatorcontrib>Maruyama, Shoichi</creatorcontrib><creatorcontrib>Matsuo, Seiichi</creatorcontrib><creatorcontrib>Nakao, Makoto</creatorcontrib><creatorcontrib>Tsuchiya, Teruo</creatorcontrib><creatorcontrib>Teramachi, Hitomi</creatorcontrib><title>Renal function evaluation in patients with cancer who were scheduled to receive carboplatin or S-1</title><title>Clinical and experimental nephrology</title><addtitle>Clin Exp Nephrol</addtitle><addtitle>Clin Exp Nephrol</addtitle><description>Background Accurate glomerular filtration rate (GFR) evaluation is significant for drug dosing of carboplatin, anticancer drug excreted mainly from kidney. Serum cystatin-C (sCys-C) is a GFR marker with little affected by body muscle mass volume. And GFR equations based on serum creatinine (eGFRcreat) and sCys-C (eGFRcys) were developed; however, accuracy of eGFRcys has not been elucidated fully among patients with cancer. Therefore, we analyzed the performance of GFR equations among patients with cancer whose GFR values were measured by inulin clearance (Cin). Methods Study design was a cross-sectional study. Subjects were 41 patients with cancer whose GFR values were measured by Cin for drug dosing studies of carboplatin or S-1 in Nagoya University Hospital from 2007 to 2010 and 29 non-cancer patients. Correlation with Cin and slope of regression line were evaluated in eGFRcreat and eGFRcys. Single and multiple regression analyses were analyzed to identify associating factors with eGFRcreat/Cin or eGFRcys/Cin. Results Age, body weight, body mass index (BMI) and sCr were different between cancer patients and non-cancer patients, but sCys-C and Cin were consistent in 2 groups. The slope of the regression line for Cin vs. eGFRcys with zero intercept in cancer patients was 1.10 (95 % CI: 1.02–1.17), which was significantly different from 1.0. In multiple regression analysis revealed that BMI and urinary creatinine excretion were significantly associated with eGFRcreat/Cin, and cancer was only associating factor with eGFRcys/Cin. Conclusion eGFRcys should not be used for evaluation of renal function in patients with cancer because it underestimates GFR.</description><subject>Aged</subject><subject>Antineoplastic Agents - adverse effects</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Body Mass Index</subject><subject>Carboplatin - adverse effects</subject><subject>Carboplatin - therapeutic use</subject><subject>Creatinine - blood</subject><subject>Cross-Sectional Studies</subject><subject>Cystatin C - blood</subject><subject>Drug Combinations</subject><subject>Female</subject><subject>Glomerular Filtration Rate</subject><subject>Humans</subject><subject>Inulin - metabolism</subject><subject>Kidney Function Tests - methods</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - physiopathology</subject><subject>Nephrology</subject><subject>Original Article</subject><subject>Oxonic Acid - adverse effects</subject><subject>Oxonic Acid - therapeutic use</subject><subject>Pyridines - adverse effects</subject><subject>Pyridines - therapeutic use</subject><subject>Tegafur - adverse effects</subject><subject>Tegafur - therapeutic use</subject><subject>Urology</subject><issn>1342-1751</issn><issn>1437-7799</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp1kUtLxDAUhYMozvj4AW4k4MZNNUmbplmK-AJB8LEOaXrjVDrJmLQz-O9NZ1REcHNyIN-5IfcgdETJGSVEnEdKKBdZkozSUbbQlBa5yISQcjv5vGAZFZxO0F6Mb4SQSnK5iyaMV7JgjExR_QhOd9gOzvStdxiWuhv02rYOL5ID10e8avsZNtoZCHg183gFAXA0M2iGDhrcexzAQLuEBIXaL7oUdNgH_JTRA7RjdRfh8OvcRy_XV8-Xt9n9w83d5cV9ZjijfQaG56LWWlZSFLzmsqqbnNuqsaQshbbCClna0lTJljk3JB-_2pCmZJYBqfN9dLqZuwj-fYDYq3kbDXSdduCHqKgopJS05GVCT_6gb34IaRFrqkoUy0eKbigTfIwBrFqEdq7Dh6JEjQWoTQEqiRoLUDRljr8mD_Ucmp_E98YTwDZATFfuFcKvp_-d-glFzJAT</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Shibata, Kanako</creator><creator>Yasuda, Yoshinari</creator><creator>Kobayashi, Ryo</creator><creator>Ando, Yuichi</creator><creator>Shimokata, Tomoya</creator><creator>Kamiya, Hideki</creator><creator>Hayashi, Mutsuharu</creator><creator>Maruyama, Shoichi</creator><creator>Matsuo, Seiichi</creator><creator>Nakao, Makoto</creator><creator>Tsuchiya, Teruo</creator><creator>Teramachi, Hitomi</creator><general>Springer Japan</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7QP</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20151201</creationdate><title>Renal function evaluation in patients with cancer who were scheduled to receive carboplatin or S-1</title><author>Shibata, Kanako ; Yasuda, Yoshinari ; Kobayashi, Ryo ; Ando, Yuichi ; Shimokata, Tomoya ; Kamiya, Hideki ; Hayashi, Mutsuharu ; Maruyama, Shoichi ; Matsuo, Seiichi ; Nakao, Makoto ; Tsuchiya, Teruo ; Teramachi, Hitomi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-ec537baa989745b598bd35f8df0667af7f796f6c8af7635c031437d0d62f2e0b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aged</topic><topic>Antineoplastic Agents - adverse effects</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Body Mass Index</topic><topic>Carboplatin - adverse effects</topic><topic>Carboplatin - therapeutic use</topic><topic>Creatinine - blood</topic><topic>Cross-Sectional Studies</topic><topic>Cystatin C - blood</topic><topic>Drug Combinations</topic><topic>Female</topic><topic>Glomerular Filtration Rate</topic><topic>Humans</topic><topic>Inulin - metabolism</topic><topic>Kidney Function Tests - methods</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Middle Aged</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - physiopathology</topic><topic>Nephrology</topic><topic>Original Article</topic><topic>Oxonic Acid - adverse effects</topic><topic>Oxonic Acid - therapeutic use</topic><topic>Pyridines - adverse effects</topic><topic>Pyridines - therapeutic use</topic><topic>Tegafur - adverse effects</topic><topic>Tegafur - therapeutic use</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shibata, Kanako</creatorcontrib><creatorcontrib>Yasuda, Yoshinari</creatorcontrib><creatorcontrib>Kobayashi, Ryo</creatorcontrib><creatorcontrib>Ando, Yuichi</creatorcontrib><creatorcontrib>Shimokata, Tomoya</creatorcontrib><creatorcontrib>Kamiya, Hideki</creatorcontrib><creatorcontrib>Hayashi, Mutsuharu</creatorcontrib><creatorcontrib>Maruyama, Shoichi</creatorcontrib><creatorcontrib>Matsuo, Seiichi</creatorcontrib><creatorcontrib>Nakao, Makoto</creatorcontrib><creatorcontrib>Tsuchiya, Teruo</creatorcontrib><creatorcontrib>Teramachi, Hitomi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical and experimental nephrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shibata, Kanako</au><au>Yasuda, Yoshinari</au><au>Kobayashi, Ryo</au><au>Ando, Yuichi</au><au>Shimokata, Tomoya</au><au>Kamiya, Hideki</au><au>Hayashi, Mutsuharu</au><au>Maruyama, Shoichi</au><au>Matsuo, Seiichi</au><au>Nakao, Makoto</au><au>Tsuchiya, Teruo</au><au>Teramachi, Hitomi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Renal function evaluation in patients with cancer who were scheduled to receive carboplatin or S-1</atitle><jtitle>Clinical and experimental nephrology</jtitle><stitle>Clin Exp Nephrol</stitle><addtitle>Clin Exp Nephrol</addtitle><date>2015-12-01</date><risdate>2015</risdate><volume>19</volume><issue>6</issue><spage>1107</spage><epage>1113</epage><pages>1107-1113</pages><issn>1342-1751</issn><eissn>1437-7799</eissn><coden>CENPFV</coden><abstract>Background Accurate glomerular filtration rate (GFR) evaluation is significant for drug dosing of carboplatin, anticancer drug excreted mainly from kidney. Serum cystatin-C (sCys-C) is a GFR marker with little affected by body muscle mass volume. And GFR equations based on serum creatinine (eGFRcreat) and sCys-C (eGFRcys) were developed; however, accuracy of eGFRcys has not been elucidated fully among patients with cancer. Therefore, we analyzed the performance of GFR equations among patients with cancer whose GFR values were measured by inulin clearance (Cin). Methods Study design was a cross-sectional study. Subjects were 41 patients with cancer whose GFR values were measured by Cin for drug dosing studies of carboplatin or S-1 in Nagoya University Hospital from 2007 to 2010 and 29 non-cancer patients. Correlation with Cin and slope of regression line were evaluated in eGFRcreat and eGFRcys. Single and multiple regression analyses were analyzed to identify associating factors with eGFRcreat/Cin or eGFRcys/Cin. Results Age, body weight, body mass index (BMI) and sCr were different between cancer patients and non-cancer patients, but sCys-C and Cin were consistent in 2 groups. The slope of the regression line for Cin vs. eGFRcys with zero intercept in cancer patients was 1.10 (95 % CI: 1.02–1.17), which was significantly different from 1.0. In multiple regression analysis revealed that BMI and urinary creatinine excretion were significantly associated with eGFRcreat/Cin, and cancer was only associating factor with eGFRcys/Cin. Conclusion eGFRcys should not be used for evaluation of renal function in patients with cancer because it underestimates GFR.</abstract><cop>Tokyo</cop><pub>Springer Japan</pub><pmid>25894220</pmid><doi>10.1007/s10157-015-1115-1</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1342-1751
ispartof Clinical and experimental nephrology, 2015-12, Vol.19 (6), p.1107-1113
issn 1342-1751
1437-7799
language eng
recordid cdi_proquest_miscellaneous_1749991656
source Springer Link
subjects Aged
Antineoplastic Agents - adverse effects
Antineoplastic Agents - therapeutic use
Antineoplastic Combined Chemotherapy Protocols - adverse effects
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Body Mass Index
Carboplatin - adverse effects
Carboplatin - therapeutic use
Creatinine - blood
Cross-Sectional Studies
Cystatin C - blood
Drug Combinations
Female
Glomerular Filtration Rate
Humans
Inulin - metabolism
Kidney Function Tests - methods
Male
Medicine
Medicine & Public Health
Middle Aged
Neoplasms - drug therapy
Neoplasms - physiopathology
Nephrology
Original Article
Oxonic Acid - adverse effects
Oxonic Acid - therapeutic use
Pyridines - adverse effects
Pyridines - therapeutic use
Tegafur - adverse effects
Tegafur - therapeutic use
Urology
title Renal function evaluation in patients with cancer who were scheduled to receive carboplatin or S-1
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T17%3A17%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Renal%20function%20evaluation%20in%20patients%20with%20cancer%20who%20were%20scheduled%20to%20receive%20carboplatin%20or%20S-1&rft.jtitle=Clinical%20and%20experimental%20nephrology&rft.au=Shibata,%20Kanako&rft.date=2015-12-01&rft.volume=19&rft.issue=6&rft.spage=1107&rft.epage=1113&rft.pages=1107-1113&rft.issn=1342-1751&rft.eissn=1437-7799&rft.coden=CENPFV&rft_id=info:doi/10.1007/s10157-015-1115-1&rft_dat=%3Cproquest_cross%3E1749991656%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c521t-ec537baa989745b598bd35f8df0667af7f796f6c8af7635c031437d0d62f2e0b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1748991236&rft_id=info:pmid/25894220&rfr_iscdi=true