Correlation between plasma concentration ratios of SN-38 glucuronide and SN-38 and neutropenia induction in patients with colorectal cancer and wild-type UGT1A1 gene
In irinotecan (CPT-11)-based chemotherapy, neutropenia and diarrhea are often induced. In the present study, the clinical significance of the concentration ratios of 7-ethyl-10-hydroxycamptothecin (SN-38) glucuronide (SN-38G) and SN-38 in the plasma in predicting CPT-11-induced neutropenia was exami...
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Veröffentlicht in: | Oncology letters 2012-03, Vol.3 (3), p.694-698 |
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creator | HIROSE, KOICHI KOZU, CHIHIRO YAMASHITA, KOSHIRO MARUO, EIJI KITAMURA, MIZUHO HASEGAWA, JUNICHI OMODA, KEI MURAKAMI, TERUO MAEDA, YORINOBU |
description | In irinotecan (CPT-11)-based chemotherapy, neutropenia and diarrhea are often induced. In the present study, the clinical significance of the concentration ratios of 7-ethyl-10-hydroxycamptothecin (SN-38) glucuronide (SN-38G) and SN-38 in the plasma in predicting CPT-11-induced neutropenia was examined. A total of 17 patients with colorectal cancer and wild-type UDP-glucuronosyltransferase (UGT)1A1 gene were enrolled and treated with CPT-11 as part of the FOLFIRI regimen [CPT-11 and fluorouracil (5-FU)]. Blood was taken exactly 15 min following a 2-h continuous infusion of CPT-11. Plasma concentrations of SN-38, SN-38G and CPT-11 were determined by a modified high-performance liquid chromatography (HPLC) method. The median, maximum and minimum values of plasma SN-38G/SN-38 ratios were 4.25, 7.09 and 1.03, respectively, indicating that UGT activities are variable among patients with the wild-type UGT1A1 gene. The plasma SN-38G/SN-38 ratios decreased with an increase in the trial numbers of chemotherapy (r=0.741, p=0.000669), suggesting that CPT-11 treatment suppresses UGT activity, and the low plasma SN-38G/SN-38 ratios resulted in the induction of greater neutropenia. However, in this analysis, 2 clearly separated regression lines were observed between plasma SN-38G/SN-38 ratios and neutropenia induction. In conclusion, UGT activity involved in SN-38 metabolism is variable among patients with the wild-type UGT1A1 gene, and each CPT-11 treatment suppresses UGT activity. One-point determination of the plasma SN-38G/SN-38 ratio may provide indications for the prediction of CPT-11-induced neutropenia and adjustment of the optimal dose, although further studies are required. |
doi_str_mv | 10.3892/ol.2011.533 |
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In the present study, the clinical significance of the concentration ratios of 7-ethyl-10-hydroxycamptothecin (SN-38) glucuronide (SN-38G) and SN-38 in the plasma in predicting CPT-11-induced neutropenia was examined. A total of 17 patients with colorectal cancer and wild-type UDP-glucuronosyltransferase (UGT)1A1 gene were enrolled and treated with CPT-11 as part of the FOLFIRI regimen [CPT-11 and fluorouracil (5-FU)]. Blood was taken exactly 15 min following a 2-h continuous infusion of CPT-11. Plasma concentrations of SN-38, SN-38G and CPT-11 were determined by a modified high-performance liquid chromatography (HPLC) method. The median, maximum and minimum values of plasma SN-38G/SN-38 ratios were 4.25, 7.09 and 1.03, respectively, indicating that UGT activities are variable among patients with the wild-type UGT1A1 gene. The plasma SN-38G/SN-38 ratios decreased with an increase in the trial numbers of chemotherapy (r=0.741, p=0.000669), suggesting that CPT-11 treatment suppresses UGT activity, and the low plasma SN-38G/SN-38 ratios resulted in the induction of greater neutropenia. However, in this analysis, 2 clearly separated regression lines were observed between plasma SN-38G/SN-38 ratios and neutropenia induction. In conclusion, UGT activity involved in SN-38 metabolism is variable among patients with the wild-type UGT1A1 gene, and each CPT-11 treatment suppresses UGT activity. One-point determination of the plasma SN-38G/SN-38 ratio may provide indications for the prediction of CPT-11-induced neutropenia and adjustment of the optimal dose, although further studies are required.</description><identifier>ISSN: 1792-1074</identifier><identifier>EISSN: 1792-1082</identifier><identifier>DOI: 10.3892/ol.2011.533</identifier><identifier>PMID: 22740978</identifier><language>eng</language><publisher>Greece: D.A. Spandidos</publisher><subject>FOLFILI regimen ; irinotecan hydrochloride ; neutropenia ; plasma SN-38G/SN-38 ratio ; polymorphism of UGT1A1 ; UDP-glucuronosyltransferase</subject><ispartof>Oncology letters, 2012-03, Vol.3 (3), p.694-698</ispartof><rights>Copyright © 2012, Spandidos Publications</rights><rights>Copyright © 2012, Spandidos Publications 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-3bee5be57c89d342a70d80bae55ad5880b98963ddd6b360fbda84618e54e93d3</citedby><cites>FETCH-LOGICAL-c412t-3bee5be57c89d342a70d80bae55ad5880b98963ddd6b360fbda84618e54e93d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3362497/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3362497/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,5556,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22740978$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HIROSE, KOICHI</creatorcontrib><creatorcontrib>KOZU, CHIHIRO</creatorcontrib><creatorcontrib>YAMASHITA, KOSHIRO</creatorcontrib><creatorcontrib>MARUO, EIJI</creatorcontrib><creatorcontrib>KITAMURA, MIZUHO</creatorcontrib><creatorcontrib>HASEGAWA, JUNICHI</creatorcontrib><creatorcontrib>OMODA, KEI</creatorcontrib><creatorcontrib>MURAKAMI, TERUO</creatorcontrib><creatorcontrib>MAEDA, YORINOBU</creatorcontrib><title>Correlation between plasma concentration ratios of SN-38 glucuronide and SN-38 and neutropenia induction in patients with colorectal cancer and wild-type UGT1A1 gene</title><title>Oncology letters</title><addtitle>Oncol Lett</addtitle><description>In irinotecan (CPT-11)-based chemotherapy, neutropenia and diarrhea are often induced. In the present study, the clinical significance of the concentration ratios of 7-ethyl-10-hydroxycamptothecin (SN-38) glucuronide (SN-38G) and SN-38 in the plasma in predicting CPT-11-induced neutropenia was examined. A total of 17 patients with colorectal cancer and wild-type UDP-glucuronosyltransferase (UGT)1A1 gene were enrolled and treated with CPT-11 as part of the FOLFIRI regimen [CPT-11 and fluorouracil (5-FU)]. Blood was taken exactly 15 min following a 2-h continuous infusion of CPT-11. Plasma concentrations of SN-38, SN-38G and CPT-11 were determined by a modified high-performance liquid chromatography (HPLC) method. The median, maximum and minimum values of plasma SN-38G/SN-38 ratios were 4.25, 7.09 and 1.03, respectively, indicating that UGT activities are variable among patients with the wild-type UGT1A1 gene. The plasma SN-38G/SN-38 ratios decreased with an increase in the trial numbers of chemotherapy (r=0.741, p=0.000669), suggesting that CPT-11 treatment suppresses UGT activity, and the low plasma SN-38G/SN-38 ratios resulted in the induction of greater neutropenia. However, in this analysis, 2 clearly separated regression lines were observed between plasma SN-38G/SN-38 ratios and neutropenia induction. In conclusion, UGT activity involved in SN-38 metabolism is variable among patients with the wild-type UGT1A1 gene, and each CPT-11 treatment suppresses UGT activity. One-point determination of the plasma SN-38G/SN-38 ratio may provide indications for the prediction of CPT-11-induced neutropenia and adjustment of the optimal dose, although further studies are required.</description><subject>FOLFILI regimen</subject><subject>irinotecan hydrochloride</subject><subject>neutropenia</subject><subject>plasma SN-38G/SN-38 ratio</subject><subject>polymorphism of UGT1A1</subject><subject>UDP-glucuronosyltransferase</subject><issn>1792-1074</issn><issn>1792-1082</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpVUU1vEzEQXSEqWpWeuCOfEBLa4I_1rn1BqiIoSBU9ND1bXnuSGjn2Yu826g_if-JkQwDL0jx53rwZz6uqNwQvmJD0Y_QLiglZcMZeVBekk7QmWNCXJ9w159VVzj9wObwlQrSvqnNKuwbLTlxUv5YxJfB6dDGgHsYdQECD13mrkYnBQBjTnDyEjOIa3X-vmUAbP5kpxeAsIB3s8XWPAkxjigMEp5ELdjKHeld0i0QRzGjnxsci72MCM2qPjC6d0qF457ytx-cB0MPNilwTtIEAr6uztfYZro7xslp9-bxafq1v726-La9va9MQOtasB-A98M4IaVlDdYetwL0GzrXlokApZMustW3PWrzurRZN2QnwBiSz7LL6NMsOU78FO3_eqyG5rU7PKmqn_s8E96g28Ukx1tJGdkXg_VEgxZ8T5FFtXTbgvQ4Qp6yIoC3nsuW0UD_MVJNizgnWpzYEq721Knq1t1YVawv77b-Tnbh_jCyEdzMhD2WLzsb8d2xfY3a4rWzYb2Q0rw8</recordid><startdate>20120301</startdate><enddate>20120301</enddate><creator>HIROSE, KOICHI</creator><creator>KOZU, CHIHIRO</creator><creator>YAMASHITA, KOSHIRO</creator><creator>MARUO, EIJI</creator><creator>KITAMURA, MIZUHO</creator><creator>HASEGAWA, JUNICHI</creator><creator>OMODA, KEI</creator><creator>MURAKAMI, TERUO</creator><creator>MAEDA, YORINOBU</creator><general>D.A. Spandidos</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120301</creationdate><title>Correlation between plasma concentration ratios of SN-38 glucuronide and SN-38 and neutropenia induction in patients with colorectal cancer and wild-type UGT1A1 gene</title><author>HIROSE, KOICHI ; KOZU, CHIHIRO ; YAMASHITA, KOSHIRO ; MARUO, EIJI ; KITAMURA, MIZUHO ; HASEGAWA, JUNICHI ; OMODA, KEI ; MURAKAMI, TERUO ; MAEDA, YORINOBU</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-3bee5be57c89d342a70d80bae55ad5880b98963ddd6b360fbda84618e54e93d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>FOLFILI regimen</topic><topic>irinotecan hydrochloride</topic><topic>neutropenia</topic><topic>plasma SN-38G/SN-38 ratio</topic><topic>polymorphism of UGT1A1</topic><topic>UDP-glucuronosyltransferase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HIROSE, KOICHI</creatorcontrib><creatorcontrib>KOZU, CHIHIRO</creatorcontrib><creatorcontrib>YAMASHITA, KOSHIRO</creatorcontrib><creatorcontrib>MARUO, EIJI</creatorcontrib><creatorcontrib>KITAMURA, MIZUHO</creatorcontrib><creatorcontrib>HASEGAWA, JUNICHI</creatorcontrib><creatorcontrib>OMODA, KEI</creatorcontrib><creatorcontrib>MURAKAMI, TERUO</creatorcontrib><creatorcontrib>MAEDA, YORINOBU</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HIROSE, KOICHI</au><au>KOZU, CHIHIRO</au><au>YAMASHITA, KOSHIRO</au><au>MARUO, EIJI</au><au>KITAMURA, MIZUHO</au><au>HASEGAWA, JUNICHI</au><au>OMODA, KEI</au><au>MURAKAMI, TERUO</au><au>MAEDA, YORINOBU</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlation between plasma concentration ratios of SN-38 glucuronide and SN-38 and neutropenia induction in patients with colorectal cancer and wild-type UGT1A1 gene</atitle><jtitle>Oncology letters</jtitle><addtitle>Oncol Lett</addtitle><date>2012-03-01</date><risdate>2012</risdate><volume>3</volume><issue>3</issue><spage>694</spage><epage>698</epage><pages>694-698</pages><issn>1792-1074</issn><eissn>1792-1082</eissn><abstract>In irinotecan (CPT-11)-based chemotherapy, neutropenia and diarrhea are often induced. In the present study, the clinical significance of the concentration ratios of 7-ethyl-10-hydroxycamptothecin (SN-38) glucuronide (SN-38G) and SN-38 in the plasma in predicting CPT-11-induced neutropenia was examined. A total of 17 patients with colorectal cancer and wild-type UDP-glucuronosyltransferase (UGT)1A1 gene were enrolled and treated with CPT-11 as part of the FOLFIRI regimen [CPT-11 and fluorouracil (5-FU)]. Blood was taken exactly 15 min following a 2-h continuous infusion of CPT-11. Plasma concentrations of SN-38, SN-38G and CPT-11 were determined by a modified high-performance liquid chromatography (HPLC) method. The median, maximum and minimum values of plasma SN-38G/SN-38 ratios were 4.25, 7.09 and 1.03, respectively, indicating that UGT activities are variable among patients with the wild-type UGT1A1 gene. The plasma SN-38G/SN-38 ratios decreased with an increase in the trial numbers of chemotherapy (r=0.741, p=0.000669), suggesting that CPT-11 treatment suppresses UGT activity, and the low plasma SN-38G/SN-38 ratios resulted in the induction of greater neutropenia. However, in this analysis, 2 clearly separated regression lines were observed between plasma SN-38G/SN-38 ratios and neutropenia induction. In conclusion, UGT activity involved in SN-38 metabolism is variable among patients with the wild-type UGT1A1 gene, and each CPT-11 treatment suppresses UGT activity. One-point determination of the plasma SN-38G/SN-38 ratio may provide indications for the prediction of CPT-11-induced neutropenia and adjustment of the optimal dose, although further studies are required.</abstract><cop>Greece</cop><pub>D.A. Spandidos</pub><pmid>22740978</pmid><doi>10.3892/ol.2011.533</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | FOLFILI regimen irinotecan hydrochloride neutropenia plasma SN-38G/SN-38 ratio polymorphism of UGT1A1 UDP-glucuronosyltransferase |
title | Correlation between plasma concentration ratios of SN-38 glucuronide and SN-38 and neutropenia induction in patients with colorectal cancer and wild-type UGT1A1 gene |
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