Serum diamine oxidase activity as a predictor of gastrointestinal toxicity and malnutrition due to anticancer drugs

Background and Aim Objective evaluation of intestinal mucosal damage due to anticancer drugs is generally difficult. Serum diamine oxidase (DAO) activity is reported to reflect the integrity and maturity of the small intestinal mucosa. Therefore, we investigated whether serum DAO activity is an indi...

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Veröffentlicht in:Journal of gastroenterology and hepatology 2015-11, Vol.30 (11), p.1582-1590
Hauptverfasser: Miyoshi, Jinsei, Miyamoto, Hiroshi, Goji, Takahiro, Taniguchi, Tatsuya, Tomonari, Tetsu, Sogabe, Masahiro, Kimura, Tetsuo, Kitamura, Shinji, Okamoto, Koichi, Fujino, Yasuteru, Muguruma, Naoki, Okahisa, Toshiya, Takayama, Tetsuji
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container_end_page 1590
container_issue 11
container_start_page 1582
container_title Journal of gastroenterology and hepatology
container_volume 30
creator Miyoshi, Jinsei
Miyamoto, Hiroshi
Goji, Takahiro
Taniguchi, Tatsuya
Tomonari, Tetsu
Sogabe, Masahiro
Kimura, Tetsuo
Kitamura, Shinji
Okamoto, Koichi
Fujino, Yasuteru
Muguruma, Naoki
Okahisa, Toshiya
Takayama, Tetsuji
description Background and Aim Objective evaluation of intestinal mucosal damage due to anticancer drugs is generally difficult. Serum diamine oxidase (DAO) activity is reported to reflect the integrity and maturity of the small intestinal mucosa. Therefore, we investigated whether serum DAO activity is an indicator of gastrointestinal toxicity or nutritional status in patients receiving chemotherapy. Methods We prospectively enrolled 20 patients with unresectable metastatic gastric cancer who received oral S‐1 (80 mg/m2) on days 1–14, and intravenous cisplatin (60 mg/m2) and docetaxel (50 mg/m2) on day 8 every 3 weeks. Serum DAO activity was measured by colorimetry. Gastrointestinal toxicity was evaluated by Common Toxicity Criteria for Adverse Events version 4.0. Endoscopic examination and biopsy of duodenal mucosa assessed mucosal damage. Malnutrition was evaluated by measuring serum total protein and albumin levels. Results Serum DAO activity decreased step‐by‐step significantly during anticancer drug treatment and recovered after drug holidays. In all 14 patients who experienced diarrhea, serum DAO activity significantly decreased prior to diarrhea onset. Percent decrease in DAO activity was significantly correlated with severity of diarrhea. Significant correlation was observed between percent decrease in DAO activity and percent decrease in duodenal villus height or surface area from baseline. There were also significant correlations between percent decrease in serum DAO activity at day 14 and percent decrease in serum total protein or albumin levels at day 21 from baseline. Conclusion Serum DAO activity sensitively indicates gastrointestinal damage prior to symptom onset and can be a useful predictor of intestinal mucosal damage and nutritional status in patients receiving chemotherapy.
doi_str_mv 10.1111/jgh.13004
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Serum diamine oxidase (DAO) activity is reported to reflect the integrity and maturity of the small intestinal mucosa. Therefore, we investigated whether serum DAO activity is an indicator of gastrointestinal toxicity or nutritional status in patients receiving chemotherapy. Methods We prospectively enrolled 20 patients with unresectable metastatic gastric cancer who received oral S‐1 (80 mg/m2) on days 1–14, and intravenous cisplatin (60 mg/m2) and docetaxel (50 mg/m2) on day 8 every 3 weeks. Serum DAO activity was measured by colorimetry. Gastrointestinal toxicity was evaluated by Common Toxicity Criteria for Adverse Events version 4.0. Endoscopic examination and biopsy of duodenal mucosa assessed mucosal damage. Malnutrition was evaluated by measuring serum total protein and albumin levels. Results Serum DAO activity decreased step‐by‐step significantly during anticancer drug treatment and recovered after drug holidays. In all 14 patients who experienced diarrhea, serum DAO activity significantly decreased prior to diarrhea onset. Percent decrease in DAO activity was significantly correlated with severity of diarrhea. Significant correlation was observed between percent decrease in DAO activity and percent decrease in duodenal villus height or surface area from baseline. There were also significant correlations between percent decrease in serum DAO activity at day 14 and percent decrease in serum total protein or albumin levels at day 21 from baseline. Conclusion Serum DAO activity sensitively indicates gastrointestinal damage prior to symptom onset and can be a useful predictor of intestinal mucosal damage and nutritional status in patients receiving chemotherapy.</description><identifier>ISSN: 0815-9319</identifier><identifier>EISSN: 1440-1746</identifier><identifier>DOI: 10.1111/jgh.13004</identifier><identifier>PMID: 25968084</identifier><language>eng</language><publisher>Australia: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Amine Oxidase (Copper-Containing) - blood ; anticancer drugs ; Antineoplastic Agents - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biomarkers - blood ; Cisplatin - administration &amp; dosage ; Cisplatin - adverse effects ; diamine oxidase ; diarrhea ; Drug Combinations ; Duodenum - drug effects ; Female ; Gastrointestinal Diseases - chemically induced ; Gastrointestinal Diseases - diagnosis ; gastrointestinal toxicity ; Humans ; Intestinal Mucosa - drug effects ; Male ; malnutrition ; Malnutrition - chemically induced ; Malnutrition - diagnosis ; Middle Aged ; Oxonic Acid - administration &amp; dosage ; Oxonic Acid - adverse effects ; Prospective Studies ; Sensitivity and Specificity ; Stomach Neoplasms - drug therapy ; Stomach Neoplasms - secondary ; Taxoids - administration &amp; dosage ; Taxoids - adverse effects ; Tegafur - administration &amp; dosage ; Tegafur - adverse effects</subject><ispartof>Journal of gastroenterology and hepatology, 2015-11, Vol.30 (11), p.1582-1590</ispartof><rights>2015 Journal of Gastroenterology and Hepatology Foundation and Wiley Publishing Asia Pty Ltd</rights><rights>2015 Journal of Gastroenterology and Hepatology Foundation and Wiley Publishing Asia Pty Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4584-11497787523b5c6b11467e0449625cbc873a5c596e7e01528f20eb8dd7eba2653</citedby><cites>FETCH-LOGICAL-c4584-11497787523b5c6b11467e0449625cbc873a5c596e7e01528f20eb8dd7eba2653</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjgh.13004$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjgh.13004$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25968084$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miyoshi, Jinsei</creatorcontrib><creatorcontrib>Miyamoto, Hiroshi</creatorcontrib><creatorcontrib>Goji, Takahiro</creatorcontrib><creatorcontrib>Taniguchi, Tatsuya</creatorcontrib><creatorcontrib>Tomonari, Tetsu</creatorcontrib><creatorcontrib>Sogabe, Masahiro</creatorcontrib><creatorcontrib>Kimura, Tetsuo</creatorcontrib><creatorcontrib>Kitamura, Shinji</creatorcontrib><creatorcontrib>Okamoto, Koichi</creatorcontrib><creatorcontrib>Fujino, Yasuteru</creatorcontrib><creatorcontrib>Muguruma, Naoki</creatorcontrib><creatorcontrib>Okahisa, Toshiya</creatorcontrib><creatorcontrib>Takayama, Tetsuji</creatorcontrib><title>Serum diamine oxidase activity as a predictor of gastrointestinal toxicity and malnutrition due to anticancer drugs</title><title>Journal of gastroenterology and hepatology</title><addtitle>J Gastroenterol Hepatol</addtitle><description>Background and Aim Objective evaluation of intestinal mucosal damage due to anticancer drugs is generally difficult. Serum diamine oxidase (DAO) activity is reported to reflect the integrity and maturity of the small intestinal mucosa. Therefore, we investigated whether serum DAO activity is an indicator of gastrointestinal toxicity or nutritional status in patients receiving chemotherapy. Methods We prospectively enrolled 20 patients with unresectable metastatic gastric cancer who received oral S‐1 (80 mg/m2) on days 1–14, and intravenous cisplatin (60 mg/m2) and docetaxel (50 mg/m2) on day 8 every 3 weeks. Serum DAO activity was measured by colorimetry. Gastrointestinal toxicity was evaluated by Common Toxicity Criteria for Adverse Events version 4.0. Endoscopic examination and biopsy of duodenal mucosa assessed mucosal damage. Malnutrition was evaluated by measuring serum total protein and albumin levels. Results Serum DAO activity decreased step‐by‐step significantly during anticancer drug treatment and recovered after drug holidays. In all 14 patients who experienced diarrhea, serum DAO activity significantly decreased prior to diarrhea onset. Percent decrease in DAO activity was significantly correlated with severity of diarrhea. Significant correlation was observed between percent decrease in DAO activity and percent decrease in duodenal villus height or surface area from baseline. There were also significant correlations between percent decrease in serum DAO activity at day 14 and percent decrease in serum total protein or albumin levels at day 21 from baseline. 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dosage</subject><subject>Oxonic Acid - adverse effects</subject><subject>Prospective Studies</subject><subject>Sensitivity and Specificity</subject><subject>Stomach Neoplasms - drug therapy</subject><subject>Stomach Neoplasms - secondary</subject><subject>Taxoids - administration &amp; dosage</subject><subject>Taxoids - adverse effects</subject><subject>Tegafur - administration &amp; dosage</subject><subject>Tegafur - adverse effects</subject><issn>0815-9319</issn><issn>1440-1746</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kDFPwzAQhS0EoqUw8AeQV4a0dmLHyYgq2lIhGApCYrEc2ykuTVLZDrT_HtPQbtxyurvvPekeANcYDXGo0Wr5McQJQuQE9DEhKMKMpKegjzJMozzBeQ9cOLdCgUCMnoNeTPM0QxnpA7fQtq2gMqIytYbN1ijhNBTSmy_jd1A4KODGamWkbyxsSrgUztvG1F47b2qxhj6I5J6tFazEum69Nd40NVStDtew90aKWmoLlW2X7hKclWLt9NVfH4DXyf3LeBY9Pk8fxnePkSQ0IxHGJGcsYzROCirTIswp04iQPI2pLGTGEkFl-ESHLaZxVsZIF5lSTBciTmkyALedr7SNc1aXfGNNJeyOY8R_g-MhOL4PLrA3Hbtpi0qrI3lIKgCjDvg2a73734nPp7ODZdQpjPN6e1QI-8lTljDK356mPJ5P3mfJYsHnyQ-wSIhR</recordid><startdate>201511</startdate><enddate>201511</enddate><creator>Miyoshi, Jinsei</creator><creator>Miyamoto, Hiroshi</creator><creator>Goji, Takahiro</creator><creator>Taniguchi, Tatsuya</creator><creator>Tomonari, Tetsu</creator><creator>Sogabe, Masahiro</creator><creator>Kimura, Tetsuo</creator><creator>Kitamura, Shinji</creator><creator>Okamoto, Koichi</creator><creator>Fujino, Yasuteru</creator><creator>Muguruma, Naoki</creator><creator>Okahisa, Toshiya</creator><creator>Takayama, Tetsuji</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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></search><sort><creationdate>201511</creationdate><title>Serum diamine oxidase activity as a predictor of gastrointestinal toxicity and malnutrition due to anticancer drugs</title><author>Miyoshi, Jinsei ; Miyamoto, Hiroshi ; Goji, Takahiro ; Taniguchi, Tatsuya ; Tomonari, Tetsu ; Sogabe, Masahiro ; Kimura, Tetsuo ; Kitamura, Shinji ; Okamoto, Koichi ; Fujino, Yasuteru ; Muguruma, Naoki ; Okahisa, Toshiya ; Takayama, Tetsuji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4584-11497787523b5c6b11467e0449625cbc873a5c596e7e01528f20eb8dd7eba2653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Amine Oxidase (Copper-Containing) - blood</topic><topic>anticancer drugs</topic><topic>Antineoplastic Agents - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biomarkers - blood</topic><topic>Cisplatin - administration &amp; dosage</topic><topic>Cisplatin - adverse effects</topic><topic>diamine oxidase</topic><topic>diarrhea</topic><topic>Drug Combinations</topic><topic>Duodenum - drug effects</topic><topic>Female</topic><topic>Gastrointestinal Diseases - chemically induced</topic><topic>Gastrointestinal Diseases - diagnosis</topic><topic>gastrointestinal toxicity</topic><topic>Humans</topic><topic>Intestinal Mucosa - drug effects</topic><topic>Male</topic><topic>malnutrition</topic><topic>Malnutrition - chemically induced</topic><topic>Malnutrition - diagnosis</topic><topic>Middle Aged</topic><topic>Oxonic Acid - administration &amp; dosage</topic><topic>Oxonic Acid - adverse effects</topic><topic>Prospective Studies</topic><topic>Sensitivity and Specificity</topic><topic>Stomach Neoplasms - drug therapy</topic><topic>Stomach Neoplasms - secondary</topic><topic>Taxoids - administration &amp; dosage</topic><topic>Taxoids - adverse effects</topic><topic>Tegafur - administration &amp; dosage</topic><topic>Tegafur - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miyoshi, Jinsei</creatorcontrib><creatorcontrib>Miyamoto, Hiroshi</creatorcontrib><creatorcontrib>Goji, Takahiro</creatorcontrib><creatorcontrib>Taniguchi, Tatsuya</creatorcontrib><creatorcontrib>Tomonari, Tetsu</creatorcontrib><creatorcontrib>Sogabe, Masahiro</creatorcontrib><creatorcontrib>Kimura, Tetsuo</creatorcontrib><creatorcontrib>Kitamura, Shinji</creatorcontrib><creatorcontrib>Okamoto, Koichi</creatorcontrib><creatorcontrib>Fujino, Yasuteru</creatorcontrib><creatorcontrib>Muguruma, Naoki</creatorcontrib><creatorcontrib>Okahisa, Toshiya</creatorcontrib><creatorcontrib>Takayama, Tetsuji</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of gastroenterology and hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miyoshi, Jinsei</au><au>Miyamoto, Hiroshi</au><au>Goji, Takahiro</au><au>Taniguchi, Tatsuya</au><au>Tomonari, Tetsu</au><au>Sogabe, Masahiro</au><au>Kimura, Tetsuo</au><au>Kitamura, Shinji</au><au>Okamoto, Koichi</au><au>Fujino, Yasuteru</au><au>Muguruma, Naoki</au><au>Okahisa, Toshiya</au><au>Takayama, Tetsuji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum diamine oxidase activity as a predictor of gastrointestinal toxicity and malnutrition due to anticancer drugs</atitle><jtitle>Journal of gastroenterology and hepatology</jtitle><addtitle>J Gastroenterol Hepatol</addtitle><date>2015-11</date><risdate>2015</risdate><volume>30</volume><issue>11</issue><spage>1582</spage><epage>1590</epage><pages>1582-1590</pages><issn>0815-9319</issn><eissn>1440-1746</eissn><abstract>Background and Aim Objective evaluation of intestinal mucosal damage due to anticancer drugs is generally difficult. Serum diamine oxidase (DAO) activity is reported to reflect the integrity and maturity of the small intestinal mucosa. Therefore, we investigated whether serum DAO activity is an indicator of gastrointestinal toxicity or nutritional status in patients receiving chemotherapy. Methods We prospectively enrolled 20 patients with unresectable metastatic gastric cancer who received oral S‐1 (80 mg/m2) on days 1–14, and intravenous cisplatin (60 mg/m2) and docetaxel (50 mg/m2) on day 8 every 3 weeks. Serum DAO activity was measured by colorimetry. Gastrointestinal toxicity was evaluated by Common Toxicity Criteria for Adverse Events version 4.0. Endoscopic examination and biopsy of duodenal mucosa assessed mucosal damage. Malnutrition was evaluated by measuring serum total protein and albumin levels. Results Serum DAO activity decreased step‐by‐step significantly during anticancer drug treatment and recovered after drug holidays. In all 14 patients who experienced diarrhea, serum DAO activity significantly decreased prior to diarrhea onset. Percent decrease in DAO activity was significantly correlated with severity of diarrhea. Significant correlation was observed between percent decrease in DAO activity and percent decrease in duodenal villus height or surface area from baseline. There were also significant correlations between percent decrease in serum DAO activity at day 14 and percent decrease in serum total protein or albumin levels at day 21 from baseline. Conclusion Serum DAO activity sensitively indicates gastrointestinal damage prior to symptom onset and can be a useful predictor of intestinal mucosal damage and nutritional status in patients receiving chemotherapy.</abstract><cop>Australia</cop><pub>Blackwell Publishing Ltd</pub><pmid>25968084</pmid><doi>10.1111/jgh.13004</doi><tpages>9</tpages></addata></record>
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subjects Adult
Aged
Amine Oxidase (Copper-Containing) - blood
anticancer drugs
Antineoplastic Agents - adverse effects
Antineoplastic Combined Chemotherapy Protocols - adverse effects
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biomarkers - blood
Cisplatin - administration & dosage
Cisplatin - adverse effects
diamine oxidase
diarrhea
Drug Combinations
Duodenum - drug effects
Female
Gastrointestinal Diseases - chemically induced
Gastrointestinal Diseases - diagnosis
gastrointestinal toxicity
Humans
Intestinal Mucosa - drug effects
Male
malnutrition
Malnutrition - chemically induced
Malnutrition - diagnosis
Middle Aged
Oxonic Acid - administration & dosage
Oxonic Acid - adverse effects
Prospective Studies
Sensitivity and Specificity
Stomach Neoplasms - drug therapy
Stomach Neoplasms - secondary
Taxoids - administration & dosage
Taxoids - adverse effects
Tegafur - administration & dosage
Tegafur - adverse effects
title Serum diamine oxidase activity as a predictor of gastrointestinal toxicity and malnutrition due to anticancer drugs
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