In vitro and in vivo evaluation of combined calcitriol and cisplatin in dogs with spontaneously occurring tumors
Purpose Calcitriol potentiates cisplatin-mediated activity in a variety of tumor models. We examine here, the effect of calcitriol and cisplatin pre-clinically and clinically in canine spontaneous tumors through in vitro studies on tumor cells and through a phase I study of calcitriol and cisplatin...
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Veröffentlicht in: | Cancer chemotherapy and pharmacology 2008-10, Vol.62 (5), p.881-891 |
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container_title | Cancer chemotherapy and pharmacology |
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creator | Rassnick, Kenneth M. Muindi, Josephia R. Johnson, Candace S. Balkman, Cheryl E. Ramnath, Nithya Yu, Wei-Dong Engler, Kristie L. Page, Rodney L. Trump, Donald L. |
description | Purpose
Calcitriol potentiates cisplatin-mediated activity in a variety of tumor models. We examine here, the effect of calcitriol and cisplatin pre-clinically and clinically in canine spontaneous tumors through in vitro studies on tumor cells and through a phase I study of calcitriol and cisplatin to identify the maximum-tolerated dosage (MTD) of this combination in dogs with cancer and to characterize the pharmacokinetic disposition of calcitriol in dogs.
Methods
Canine tumor cells were investigated for calcitriol/cisplatin interactions on proliferation using an MTT assay in a median-dose effect analysis; data were used to derive a combination index (CI). Cisplatin was given at a fixed dosage of 60 mg/m
2
. Calcitriol was given i.v. and the dosage was escalated in cohorts of three dogs until the MTD was defined. Serum calcitriol concentrations were quantified by radioimmunoassay.
Results
In vitro, CIs 1.5 μg/kg achieved
C
max
≥ 9.8 ng/mL and dosages >1.0 μg/kg achieved AUC ≥ 45 h ng/mL.
Conclusions
Calcitriol and cisplatin have synergistic antiproliferative effects on multiple canine tumor cells and high-dosages of i.v. calcitriol in combination with cisplatin can be safely administered to dogs.
C
max
and AUC at the MTD 3.75 μg/kg calcitriol exceed concentrations associated with antitumor activity in a murine model, indicating this combination might have significant clinical utility in dogs. |
doi_str_mv | 10.1007/s00280-008-0678-x |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2715945</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1536964301</sourcerecordid><originalsourceid>FETCH-LOGICAL-c497t-51c4a2f3e2cc013f2b2b946b1f9f80c81032198e74a3141033977b22ea5dd8953</originalsourceid><addsrcrecordid>eNp1kUtLJDEUhYMo2jrzA2YzBMFl6c2jupKNIOILhNnMrEMqleqOVCdlUtXqvzdlN60uZhUu-c65l3MQ-kXgnABUFwmACigARAHzShSve2hGOKMFCM720QwY50VZAT9Cxyk9AQAnjB2iIyIonzMuZ6h_8Hjthhiw9g1207AO2K51N-rBBY9Di01Y1c7bBhvdmcy60H3QxqW-y5SfdE1YJPzihiVOffCD9jaMqXvDwZgxRucXeBhXIaYf6KDVXbI_t-8J-nd78_f6vnj8c_dwffVYGC6roSiJ4Zq2zFJjgLCW1rSWfF6TVrYCjCDAKJHCVlwzwvPEZFXVlFpdNo2QJTtBlxvffqxXtjHWD1F3qo9upeObCtqp7z_eLdUirBWtSCn5ZHC6NYjhebRpUE9hjD7frChhXIAkNENkA5kYUoq23S0goKaO1KYjlTtSU0fqNWt-f73sU7EtJQNnW0CnHHkbtc9R7zgKcwpSsMzRDZf6KWAbPy_8__Z3jB-sOg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>213480912</pqid></control><display><type>article</type><title>In vitro and in vivo evaluation of combined calcitriol and cisplatin in dogs with spontaneously occurring tumors</title><source>MEDLINE</source><source>SpringerLink Journals</source><creator>Rassnick, Kenneth M. ; Muindi, Josephia R. ; Johnson, Candace S. ; Balkman, Cheryl E. ; Ramnath, Nithya ; Yu, Wei-Dong ; Engler, Kristie L. ; Page, Rodney L. ; Trump, Donald L.</creator><creatorcontrib>Rassnick, Kenneth M. ; Muindi, Josephia R. ; Johnson, Candace S. ; Balkman, Cheryl E. ; Ramnath, Nithya ; Yu, Wei-Dong ; Engler, Kristie L. ; Page, Rodney L. ; Trump, Donald L.</creatorcontrib><description>Purpose
Calcitriol potentiates cisplatin-mediated activity in a variety of tumor models. We examine here, the effect of calcitriol and cisplatin pre-clinically and clinically in canine spontaneous tumors through in vitro studies on tumor cells and through a phase I study of calcitriol and cisplatin to identify the maximum-tolerated dosage (MTD) of this combination in dogs with cancer and to characterize the pharmacokinetic disposition of calcitriol in dogs.
Methods
Canine tumor cells were investigated for calcitriol/cisplatin interactions on proliferation using an MTT assay in a median-dose effect analysis; data were used to derive a combination index (CI). Cisplatin was given at a fixed dosage of 60 mg/m
2
. Calcitriol was given i.v. and the dosage was escalated in cohorts of three dogs until the MTD was defined. Serum calcitriol concentrations were quantified by radioimmunoassay.
Results
In vitro, CIs < 1.0 were obtained for all combinations of calcitriol/cisplatin examined. The MTD was 3.75 μg/kg calcitriol in combination with cisplatin, and hypercalcemia was the dose-limiting toxicosis. The relationship between calcitriol dosage and either
C
max
or AUC was linear. Calcitriol dosages >1.5 μg/kg achieved
C
max
≥ 9.8 ng/mL and dosages >1.0 μg/kg achieved AUC ≥ 45 h ng/mL.
Conclusions
Calcitriol and cisplatin have synergistic antiproliferative effects on multiple canine tumor cells and high-dosages of i.v. calcitriol in combination with cisplatin can be safely administered to dogs.
C
max
and AUC at the MTD 3.75 μg/kg calcitriol exceed concentrations associated with antitumor activity in a murine model, indicating this combination might have significant clinical utility in dogs.</description><identifier>ISSN: 0344-5704</identifier><identifier>EISSN: 1432-0843</identifier><identifier>DOI: 10.1007/s00280-008-0678-x</identifier><identifier>PMID: 18246349</identifier><identifier>CODEN: CCPHDZ</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Animals ; Antineoplastic agents ; Antineoplastic Agents - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - pharmacokinetics ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Area Under Curve ; Biological and medical sciences ; Calcitriol - administration & dosage ; Cancer Research ; Cell Line, Tumor ; Cisplatin - administration & dosage ; Dog Diseases - drug therapy ; Dogs ; Dose-Response Relationship, Drug ; Drug Hypersensitivity - epidemiology ; Gastrointestinal Diseases - chemically induced ; Gastrointestinal Diseases - epidemiology ; Hematologic Diseases - chemically induced ; Hematologic Diseases - epidemiology ; Injections, Intravenous ; Medical sciences ; Medicine ; Medicine & Public Health ; Neoplasms - drug therapy ; Neoplasms - veterinary ; Oncology ; Original ; Original Article ; Pharmacology. Drug treatments ; Pharmacology/Toxicology ; Tetrazolium Salts ; Thiazoles ; Vitamins - administration & dosage</subject><ispartof>Cancer chemotherapy and pharmacology, 2008-10, Vol.62 (5), p.881-891</ispartof><rights>Springer-Verlag 2008</rights><rights>2008 INIST-CNRS</rights><rights>Springer-Verlag 2008 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c497t-51c4a2f3e2cc013f2b2b946b1f9f80c81032198e74a3141033977b22ea5dd8953</citedby><cites>FETCH-LOGICAL-c497t-51c4a2f3e2cc013f2b2b946b1f9f80c81032198e74a3141033977b22ea5dd8953</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00280-008-0678-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00280-008-0678-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20620983$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18246349$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rassnick, Kenneth M.</creatorcontrib><creatorcontrib>Muindi, Josephia R.</creatorcontrib><creatorcontrib>Johnson, Candace S.</creatorcontrib><creatorcontrib>Balkman, Cheryl E.</creatorcontrib><creatorcontrib>Ramnath, Nithya</creatorcontrib><creatorcontrib>Yu, Wei-Dong</creatorcontrib><creatorcontrib>Engler, Kristie L.</creatorcontrib><creatorcontrib>Page, Rodney L.</creatorcontrib><creatorcontrib>Trump, Donald L.</creatorcontrib><title>In vitro and in vivo evaluation of combined calcitriol and cisplatin in dogs with spontaneously occurring tumors</title><title>Cancer chemotherapy and pharmacology</title><addtitle>Cancer Chemother Pharmacol</addtitle><addtitle>Cancer Chemother Pharmacol</addtitle><description>Purpose
Calcitriol potentiates cisplatin-mediated activity in a variety of tumor models. We examine here, the effect of calcitriol and cisplatin pre-clinically and clinically in canine spontaneous tumors through in vitro studies on tumor cells and through a phase I study of calcitriol and cisplatin to identify the maximum-tolerated dosage (MTD) of this combination in dogs with cancer and to characterize the pharmacokinetic disposition of calcitriol in dogs.
Methods
Canine tumor cells were investigated for calcitriol/cisplatin interactions on proliferation using an MTT assay in a median-dose effect analysis; data were used to derive a combination index (CI). Cisplatin was given at a fixed dosage of 60 mg/m
2
. Calcitriol was given i.v. and the dosage was escalated in cohorts of three dogs until the MTD was defined. Serum calcitriol concentrations were quantified by radioimmunoassay.
Results
In vitro, CIs < 1.0 were obtained for all combinations of calcitriol/cisplatin examined. The MTD was 3.75 μg/kg calcitriol in combination with cisplatin, and hypercalcemia was the dose-limiting toxicosis. The relationship between calcitriol dosage and either
C
max
or AUC was linear. Calcitriol dosages >1.5 μg/kg achieved
C
max
≥ 9.8 ng/mL and dosages >1.0 μg/kg achieved AUC ≥ 45 h ng/mL.
Conclusions
Calcitriol and cisplatin have synergistic antiproliferative effects on multiple canine tumor cells and high-dosages of i.v. calcitriol in combination with cisplatin can be safely administered to dogs.
C
max
and AUC at the MTD 3.75 μg/kg calcitriol exceed concentrations associated with antitumor activity in a murine model, indicating this combination might have significant clinical utility in dogs.</description><subject>Animals</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - pharmacokinetics</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Area Under Curve</subject><subject>Biological and medical sciences</subject><subject>Calcitriol - administration & dosage</subject><subject>Cancer Research</subject><subject>Cell Line, Tumor</subject><subject>Cisplatin - administration & dosage</subject><subject>Dog Diseases - drug therapy</subject><subject>Dogs</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Hypersensitivity - epidemiology</subject><subject>Gastrointestinal Diseases - chemically induced</subject><subject>Gastrointestinal Diseases - epidemiology</subject><subject>Hematologic Diseases - chemically induced</subject><subject>Hematologic Diseases - epidemiology</subject><subject>Injections, Intravenous</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - veterinary</subject><subject>Oncology</subject><subject>Original</subject><subject>Original Article</subject><subject>Pharmacology. Drug treatments</subject><subject>Pharmacology/Toxicology</subject><subject>Tetrazolium Salts</subject><subject>Thiazoles</subject><subject>Vitamins - administration & dosage</subject><issn>0344-5704</issn><issn>1432-0843</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kUtLJDEUhYMo2jrzA2YzBMFl6c2jupKNIOILhNnMrEMqleqOVCdlUtXqvzdlN60uZhUu-c65l3MQ-kXgnABUFwmACigARAHzShSve2hGOKMFCM720QwY50VZAT9Cxyk9AQAnjB2iIyIonzMuZ6h_8Hjthhiw9g1207AO2K51N-rBBY9Di01Y1c7bBhvdmcy60H3QxqW-y5SfdE1YJPzihiVOffCD9jaMqXvDwZgxRucXeBhXIaYf6KDVXbI_t-8J-nd78_f6vnj8c_dwffVYGC6roSiJ4Zq2zFJjgLCW1rSWfF6TVrYCjCDAKJHCVlwzwvPEZFXVlFpdNo2QJTtBlxvffqxXtjHWD1F3qo9upeObCtqp7z_eLdUirBWtSCn5ZHC6NYjhebRpUE9hjD7frChhXIAkNENkA5kYUoq23S0goKaO1KYjlTtSU0fqNWt-f73sU7EtJQNnW0CnHHkbtc9R7zgKcwpSsMzRDZf6KWAbPy_8__Z3jB-sOg</recordid><startdate>20081001</startdate><enddate>20081001</enddate><creator>Rassnick, Kenneth M.</creator><creator>Muindi, Josephia R.</creator><creator>Johnson, Candace S.</creator><creator>Balkman, Cheryl E.</creator><creator>Ramnath, Nithya</creator><creator>Yu, Wei-Dong</creator><creator>Engler, Kristie L.</creator><creator>Page, Rodney L.</creator><creator>Trump, Donald L.</creator><general>Springer-Verlag</general><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</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>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>5PM</scope></search><sort><creationdate>20081001</creationdate><title>In vitro and in vivo evaluation of combined calcitriol and cisplatin in dogs with spontaneously occurring tumors</title><author>Rassnick, Kenneth M. ; Muindi, Josephia R. ; Johnson, Candace S. ; Balkman, Cheryl E. ; Ramnath, Nithya ; Yu, Wei-Dong ; Engler, Kristie L. ; Page, Rodney L. ; Trump, Donald L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c497t-51c4a2f3e2cc013f2b2b946b1f9f80c81032198e74a3141033977b22ea5dd8953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - pharmacokinetics</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Area Under Curve</topic><topic>Biological and medical sciences</topic><topic>Calcitriol - administration & dosage</topic><topic>Cancer Research</topic><topic>Cell Line, Tumor</topic><topic>Cisplatin - administration & dosage</topic><topic>Dog Diseases - drug therapy</topic><topic>Dogs</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Hypersensitivity - epidemiology</topic><topic>Gastrointestinal Diseases - chemically induced</topic><topic>Gastrointestinal Diseases - epidemiology</topic><topic>Hematologic Diseases - chemically induced</topic><topic>Hematologic Diseases - epidemiology</topic><topic>Injections, Intravenous</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - veterinary</topic><topic>Oncology</topic><topic>Original</topic><topic>Original Article</topic><topic>Pharmacology. Drug treatments</topic><topic>Pharmacology/Toxicology</topic><topic>Tetrazolium Salts</topic><topic>Thiazoles</topic><topic>Vitamins - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rassnick, Kenneth M.</creatorcontrib><creatorcontrib>Muindi, Josephia R.</creatorcontrib><creatorcontrib>Johnson, Candace S.</creatorcontrib><creatorcontrib>Balkman, Cheryl E.</creatorcontrib><creatorcontrib>Ramnath, Nithya</creatorcontrib><creatorcontrib>Yu, Wei-Dong</creatorcontrib><creatorcontrib>Engler, Kristie L.</creatorcontrib><creatorcontrib>Page, Rodney L.</creatorcontrib><creatorcontrib>Trump, Donald L.</creatorcontrib><collection>Pascal-Francis</collection><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>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</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 Edition)</collection><collection>ProQuest Central UK/Ireland</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>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & 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>PubMed Central (Full Participant titles)</collection><jtitle>Cancer chemotherapy and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rassnick, Kenneth M.</au><au>Muindi, Josephia R.</au><au>Johnson, Candace S.</au><au>Balkman, Cheryl E.</au><au>Ramnath, Nithya</au><au>Yu, Wei-Dong</au><au>Engler, Kristie L.</au><au>Page, Rodney L.</au><au>Trump, Donald L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro and in vivo evaluation of combined calcitriol and cisplatin in dogs with spontaneously occurring tumors</atitle><jtitle>Cancer chemotherapy and pharmacology</jtitle><stitle>Cancer Chemother Pharmacol</stitle><addtitle>Cancer Chemother Pharmacol</addtitle><date>2008-10-01</date><risdate>2008</risdate><volume>62</volume><issue>5</issue><spage>881</spage><epage>891</epage><pages>881-891</pages><issn>0344-5704</issn><eissn>1432-0843</eissn><coden>CCPHDZ</coden><abstract>Purpose
Calcitriol potentiates cisplatin-mediated activity in a variety of tumor models. We examine here, the effect of calcitriol and cisplatin pre-clinically and clinically in canine spontaneous tumors through in vitro studies on tumor cells and through a phase I study of calcitriol and cisplatin to identify the maximum-tolerated dosage (MTD) of this combination in dogs with cancer and to characterize the pharmacokinetic disposition of calcitriol in dogs.
Methods
Canine tumor cells were investigated for calcitriol/cisplatin interactions on proliferation using an MTT assay in a median-dose effect analysis; data were used to derive a combination index (CI). Cisplatin was given at a fixed dosage of 60 mg/m
2
. Calcitriol was given i.v. and the dosage was escalated in cohorts of three dogs until the MTD was defined. Serum calcitriol concentrations were quantified by radioimmunoassay.
Results
In vitro, CIs < 1.0 were obtained for all combinations of calcitriol/cisplatin examined. The MTD was 3.75 μg/kg calcitriol in combination with cisplatin, and hypercalcemia was the dose-limiting toxicosis. The relationship between calcitriol dosage and either
C
max
or AUC was linear. Calcitriol dosages >1.5 μg/kg achieved
C
max
≥ 9.8 ng/mL and dosages >1.0 μg/kg achieved AUC ≥ 45 h ng/mL.
Conclusions
Calcitriol and cisplatin have synergistic antiproliferative effects on multiple canine tumor cells and high-dosages of i.v. calcitriol in combination with cisplatin can be safely administered to dogs.
C
max
and AUC at the MTD 3.75 μg/kg calcitriol exceed concentrations associated with antitumor activity in a murine model, indicating this combination might have significant clinical utility in dogs.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>18246349</pmid><doi>10.1007/s00280-008-0678-x</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antineoplastic agents Antineoplastic Agents - administration & dosage Antineoplastic Combined Chemotherapy Protocols - pharmacokinetics Antineoplastic Combined Chemotherapy Protocols - therapeutic use Area Under Curve Biological and medical sciences Calcitriol - administration & dosage Cancer Research Cell Line, Tumor Cisplatin - administration & dosage Dog Diseases - drug therapy Dogs Dose-Response Relationship, Drug Drug Hypersensitivity - epidemiology Gastrointestinal Diseases - chemically induced Gastrointestinal Diseases - epidemiology Hematologic Diseases - chemically induced Hematologic Diseases - epidemiology Injections, Intravenous Medical sciences Medicine Medicine & Public Health Neoplasms - drug therapy Neoplasms - veterinary Oncology Original Original Article Pharmacology. Drug treatments Pharmacology/Toxicology Tetrazolium Salts Thiazoles Vitamins - administration & dosage |
title | In vitro and in vivo evaluation of combined calcitriol and cisplatin in dogs with spontaneously occurring tumors |
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