A phase II trial of dexamethasone, vitamin D, and carboplatin in patients with hormone‐refractory prostate cancer
BACKGROUND. A Phase II prospective trial was performed to study the efficacy of combination therapy with dexamethasone, calcitriol (1,25‐dihydroxyvitamin D3), and carboplatin in patients with hormone‐refractory prostate cancer (HRPC). Preclinical data from prostate cancer cell lines suggested a syne...
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creator | Flaig, Thomas W. Barqawi, Albaha Miller, Gary Kane, Madeleine Zeng, Chan Crawford, E. David Glodé, L. Michael |
description | BACKGROUND.
A Phase II prospective trial was performed to study the efficacy of combination therapy with dexamethasone, calcitriol (1,25‐dihydroxyvitamin D3), and carboplatin in patients with hormone‐refractory prostate cancer (HRPC). Preclinical data from prostate cancer cell lines suggested a synergistic effect of these therapies.
METHODS.
All patients had pathologically confirmed prostate cancer with at least 2 consecutive increases in prostate‐specific antigen (PSA). Treatment started with 1 mg of oral dexamethasone given daily with 0.5 mcg of daily calcitriol added at the start of Week 5. Carboplatin (area under the concentration time curve = 2) was started at the beginning of Week 7. Initially, carboplatin was given weekly; however, the protocol was changed later to give carboplatin for the first 4 weeks of a 6‐week cycle. Of 40 patients who consented to participate, 6 patients were ineligible or declined to start therapy, leaving 34 treated patients. The median follow‐up was 80.7 weeks (range, 11.5–260 weeks).
RESULTS.
A formal PSA response was seen in 13 of 34 treated patients (38.2%; 95% confidence interval [95% CI], 22.2–56.4%). The median overall survival was 97.7 weeks (95% CI, 61–114 weeks). Significant adverse events that were observed during the trial period included 2 deaths (myocardial infarction and cardiogenic shock), 4 patients with Grade 3 neutropenia (according to the National Cancer Institute Common Toxicity Criteria, version 2.0), 2 patients with thrombosis, 2 patients with inflammatory bowel symptoms, and 2 patients with new‐onset diabetes mellitus.
CONCLUSIONS.
The novel combination of dexamethasone, calcitriol, and carboplatin for patients with HRPC produced a PSA response in 13 of 34 patients and had an acceptable side‐effect profile. Cancer 2006. © 2006 American Cancer Society.
Metronomic therapy is the frequent administration of low‐dose treatment. In this article, the authors report on the efficacy of metronomic calcitriol and dexamethasone in combination with carboplatin for the treatment of patients with hormone‐refractory prostate cancer. |
doi_str_mv | 10.1002/cncr.21982 |
format | Article |
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A Phase II prospective trial was performed to study the efficacy of combination therapy with dexamethasone, calcitriol (1,25‐dihydroxyvitamin D3), and carboplatin in patients with hormone‐refractory prostate cancer (HRPC). Preclinical data from prostate cancer cell lines suggested a synergistic effect of these therapies.
METHODS.
All patients had pathologically confirmed prostate cancer with at least 2 consecutive increases in prostate‐specific antigen (PSA). Treatment started with 1 mg of oral dexamethasone given daily with 0.5 mcg of daily calcitriol added at the start of Week 5. Carboplatin (area under the concentration time curve = 2) was started at the beginning of Week 7. Initially, carboplatin was given weekly; however, the protocol was changed later to give carboplatin for the first 4 weeks of a 6‐week cycle. Of 40 patients who consented to participate, 6 patients were ineligible or declined to start therapy, leaving 34 treated patients. The median follow‐up was 80.7 weeks (range, 11.5–260 weeks).
RESULTS.
A formal PSA response was seen in 13 of 34 treated patients (38.2%; 95% confidence interval [95% CI], 22.2–56.4%). The median overall survival was 97.7 weeks (95% CI, 61–114 weeks). Significant adverse events that were observed during the trial period included 2 deaths (myocardial infarction and cardiogenic shock), 4 patients with Grade 3 neutropenia (according to the National Cancer Institute Common Toxicity Criteria, version 2.0), 2 patients with thrombosis, 2 patients with inflammatory bowel symptoms, and 2 patients with new‐onset diabetes mellitus.
CONCLUSIONS.
The novel combination of dexamethasone, calcitriol, and carboplatin for patients with HRPC produced a PSA response in 13 of 34 patients and had an acceptable side‐effect profile. Cancer 2006. © 2006 American Cancer Society.
Metronomic therapy is the frequent administration of low‐dose treatment. In this article, the authors report on the efficacy of metronomic calcitriol and dexamethasone in combination with carboplatin for the treatment of patients with hormone‐refractory prostate cancer.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.21982</identifier><identifier>PMID: 16779800</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Aged ; Aged, 80 and over ; Androgen Antagonists - therapeutic use ; antineoplastic combined chemotherapy protocols ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; carboplatin ; Carboplatin - administration & dosage ; Carboplatin - adverse effects ; Carboplatin - therapeutic use ; dexamethasone ; Dexamethasone - administration & dosage ; Dexamethasone - adverse effects ; Dexamethasone - therapeutic use ; human ; Humans ; Male ; Medical sciences ; metronomic ; Middle Aged ; Nephrology. Urinary tract diseases ; prostate neoplasms ; Prostate-Specific Antigen - blood ; prostate‐specific antigen ; Prostatic Neoplasms - diagnosis ; Prostatic Neoplasms - drug therapy ; Prostatic Neoplasms - mortality ; Treatment Outcome ; Tumors ; Tumors of the urinary system ; Urinary tract. Prostate gland ; vitamin D ; Vitamin D - administration & dosage ; Vitamin D - adverse effects ; Vitamin D - blood ; Vitamin D - therapeutic use</subject><ispartof>Cancer, 2006-07, Vol.107 (2), p.266-274</ispartof><rights>Copyright © 2006 American Cancer Society</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4242-3a60c5a236f6bf2ddb9619367319b26382c843cfa9d5e4aee61eb6769f7e02133</citedby><cites>FETCH-LOGICAL-c4242-3a60c5a236f6bf2ddb9619367319b26382c843cfa9d5e4aee61eb6769f7e02133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcncr.21982$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcncr.21982$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17935166$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16779800$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Flaig, Thomas W.</creatorcontrib><creatorcontrib>Barqawi, Albaha</creatorcontrib><creatorcontrib>Miller, Gary</creatorcontrib><creatorcontrib>Kane, Madeleine</creatorcontrib><creatorcontrib>Zeng, Chan</creatorcontrib><creatorcontrib>Crawford, E. David</creatorcontrib><creatorcontrib>Glodé, L. Michael</creatorcontrib><title>A phase II trial of dexamethasone, vitamin D, and carboplatin in patients with hormone‐refractory prostate cancer</title><title>Cancer</title><addtitle>Cancer</addtitle><description>BACKGROUND.
A Phase II prospective trial was performed to study the efficacy of combination therapy with dexamethasone, calcitriol (1,25‐dihydroxyvitamin D3), and carboplatin in patients with hormone‐refractory prostate cancer (HRPC). Preclinical data from prostate cancer cell lines suggested a synergistic effect of these therapies.
METHODS.
All patients had pathologically confirmed prostate cancer with at least 2 consecutive increases in prostate‐specific antigen (PSA). Treatment started with 1 mg of oral dexamethasone given daily with 0.5 mcg of daily calcitriol added at the start of Week 5. Carboplatin (area under the concentration time curve = 2) was started at the beginning of Week 7. Initially, carboplatin was given weekly; however, the protocol was changed later to give carboplatin for the first 4 weeks of a 6‐week cycle. Of 40 patients who consented to participate, 6 patients were ineligible or declined to start therapy, leaving 34 treated patients. The median follow‐up was 80.7 weeks (range, 11.5–260 weeks).
RESULTS.
A formal PSA response was seen in 13 of 34 treated patients (38.2%; 95% confidence interval [95% CI], 22.2–56.4%). The median overall survival was 97.7 weeks (95% CI, 61–114 weeks). Significant adverse events that were observed during the trial period included 2 deaths (myocardial infarction and cardiogenic shock), 4 patients with Grade 3 neutropenia (according to the National Cancer Institute Common Toxicity Criteria, version 2.0), 2 patients with thrombosis, 2 patients with inflammatory bowel symptoms, and 2 patients with new‐onset diabetes mellitus.
CONCLUSIONS.
The novel combination of dexamethasone, calcitriol, and carboplatin for patients with HRPC produced a PSA response in 13 of 34 patients and had an acceptable side‐effect profile. Cancer 2006. © 2006 American Cancer Society.
Metronomic therapy is the frequent administration of low‐dose treatment. In this article, the authors report on the efficacy of metronomic calcitriol and dexamethasone in combination with carboplatin for the treatment of patients with hormone‐refractory prostate cancer.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Androgen Antagonists - therapeutic use</subject><subject>antineoplastic combined chemotherapy protocols</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>carboplatin</subject><subject>Carboplatin - administration & dosage</subject><subject>Carboplatin - adverse effects</subject><subject>Carboplatin - therapeutic use</subject><subject>dexamethasone</subject><subject>Dexamethasone - administration & dosage</subject><subject>Dexamethasone - adverse effects</subject><subject>Dexamethasone - therapeutic use</subject><subject>human</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>metronomic</subject><subject>Middle Aged</subject><subject>Nephrology. Urinary tract diseases</subject><subject>prostate neoplasms</subject><subject>Prostate-Specific Antigen - blood</subject><subject>prostate‐specific antigen</subject><subject>Prostatic Neoplasms - diagnosis</subject><subject>Prostatic Neoplasms - drug therapy</subject><subject>Prostatic Neoplasms - mortality</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><subject>Tumors of the urinary system</subject><subject>Urinary tract. Prostate gland</subject><subject>vitamin D</subject><subject>Vitamin D - administration & dosage</subject><subject>Vitamin D - adverse effects</subject><subject>Vitamin D - blood</subject><subject>Vitamin D - therapeutic use</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKxDAUhoMoOl42PoBkowuxmkubNsthvA2Igii4K6fpKVPpzSSjzs5H8Bl9EqMz4E4IJDl85_yHj5B9zk45Y-LMdMaeCq4zsUZGnOk0YjwW62TEGMuiJJZPW2TbuefwTUUiN8kWV2mqM8ZGxI3pMAOHdDql3tbQ0L6iJb5Diz7U-w5P6Gvtoa07en5CoSupAVv0QwM-lMIZwgM77-hb7Wd01ts2NH19fFqsLBjf2wUdbO88eAytnUG7SzYqaBzure4d8nh58TC5jm7urqaT8U1kYhGLSIJiJgEhVaWKSpRloRXXUqWS60IomQmTxdJUoMsEY0BUHAuVKl2lyASXcoccLeeG_Jc5Op-3tTPYNNBhP3e54CJTXCYBPF6CJizqwuL5YOsW7CLnLP9RnP8ozn8VB_hgNXVetFj-oSunAThcAeAMNMFCZ2r3x6VaJlypwPEl91Y3uPgnMp_cTu6X4d9a0JVC</recordid><startdate>20060715</startdate><enddate>20060715</enddate><creator>Flaig, Thomas W.</creator><creator>Barqawi, Albaha</creator><creator>Miller, Gary</creator><creator>Kane, Madeleine</creator><creator>Zeng, Chan</creator><creator>Crawford, E. David</creator><creator>Glodé, L. Michael</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</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>7U7</scope><scope>C1K</scope></search><sort><creationdate>20060715</creationdate><title>A phase II trial of dexamethasone, vitamin D, and carboplatin in patients with hormone‐refractory prostate cancer</title><author>Flaig, Thomas W. ; Barqawi, Albaha ; Miller, Gary ; Kane, Madeleine ; Zeng, Chan ; Crawford, E. David ; Glodé, L. Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4242-3a60c5a236f6bf2ddb9619367319b26382c843cfa9d5e4aee61eb6769f7e02133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Androgen Antagonists - therapeutic use</topic><topic>antineoplastic combined chemotherapy protocols</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>carboplatin</topic><topic>Carboplatin - administration & dosage</topic><topic>Carboplatin - adverse effects</topic><topic>Carboplatin - therapeutic use</topic><topic>dexamethasone</topic><topic>Dexamethasone - administration & dosage</topic><topic>Dexamethasone - adverse effects</topic><topic>Dexamethasone - therapeutic use</topic><topic>human</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>metronomic</topic><topic>Middle Aged</topic><topic>Nephrology. Urinary tract diseases</topic><topic>prostate neoplasms</topic><topic>Prostate-Specific Antigen - blood</topic><topic>prostate‐specific antigen</topic><topic>Prostatic Neoplasms - diagnosis</topic><topic>Prostatic Neoplasms - drug therapy</topic><topic>Prostatic Neoplasms - mortality</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><topic>Tumors of the urinary system</topic><topic>Urinary tract. Prostate gland</topic><topic>vitamin D</topic><topic>Vitamin D - administration & dosage</topic><topic>Vitamin D - adverse effects</topic><topic>Vitamin D - blood</topic><topic>Vitamin D - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Flaig, Thomas W.</creatorcontrib><creatorcontrib>Barqawi, Albaha</creatorcontrib><creatorcontrib>Miller, Gary</creatorcontrib><creatorcontrib>Kane, Madeleine</creatorcontrib><creatorcontrib>Zeng, Chan</creatorcontrib><creatorcontrib>Crawford, E. David</creatorcontrib><creatorcontrib>Glodé, L. Michael</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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Flaig, Thomas W.</au><au>Barqawi, Albaha</au><au>Miller, Gary</au><au>Kane, Madeleine</au><au>Zeng, Chan</au><au>Crawford, E. David</au><au>Glodé, L. Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A phase II trial of dexamethasone, vitamin D, and carboplatin in patients with hormone‐refractory prostate cancer</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2006-07-15</date><risdate>2006</risdate><volume>107</volume><issue>2</issue><spage>266</spage><epage>274</epage><pages>266-274</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>BACKGROUND.
A Phase II prospective trial was performed to study the efficacy of combination therapy with dexamethasone, calcitriol (1,25‐dihydroxyvitamin D3), and carboplatin in patients with hormone‐refractory prostate cancer (HRPC). Preclinical data from prostate cancer cell lines suggested a synergistic effect of these therapies.
METHODS.
All patients had pathologically confirmed prostate cancer with at least 2 consecutive increases in prostate‐specific antigen (PSA). Treatment started with 1 mg of oral dexamethasone given daily with 0.5 mcg of daily calcitriol added at the start of Week 5. Carboplatin (area under the concentration time curve = 2) was started at the beginning of Week 7. Initially, carboplatin was given weekly; however, the protocol was changed later to give carboplatin for the first 4 weeks of a 6‐week cycle. Of 40 patients who consented to participate, 6 patients were ineligible or declined to start therapy, leaving 34 treated patients. The median follow‐up was 80.7 weeks (range, 11.5–260 weeks).
RESULTS.
A formal PSA response was seen in 13 of 34 treated patients (38.2%; 95% confidence interval [95% CI], 22.2–56.4%). The median overall survival was 97.7 weeks (95% CI, 61–114 weeks). Significant adverse events that were observed during the trial period included 2 deaths (myocardial infarction and cardiogenic shock), 4 patients with Grade 3 neutropenia (according to the National Cancer Institute Common Toxicity Criteria, version 2.0), 2 patients with thrombosis, 2 patients with inflammatory bowel symptoms, and 2 patients with new‐onset diabetes mellitus.
CONCLUSIONS.
The novel combination of dexamethasone, calcitriol, and carboplatin for patients with HRPC produced a PSA response in 13 of 34 patients and had an acceptable side‐effect profile. Cancer 2006. © 2006 American Cancer Society.
Metronomic therapy is the frequent administration of low‐dose treatment. In this article, the authors report on the efficacy of metronomic calcitriol and dexamethasone in combination with carboplatin for the treatment of patients with hormone‐refractory prostate cancer.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>16779800</pmid><doi>10.1002/cncr.21982</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aged, 80 and over Androgen Antagonists - therapeutic use antineoplastic combined chemotherapy protocols Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences carboplatin Carboplatin - administration & dosage Carboplatin - adverse effects Carboplatin - therapeutic use dexamethasone Dexamethasone - administration & dosage Dexamethasone - adverse effects Dexamethasone - therapeutic use human Humans Male Medical sciences metronomic Middle Aged Nephrology. Urinary tract diseases prostate neoplasms Prostate-Specific Antigen - blood prostate‐specific antigen Prostatic Neoplasms - diagnosis Prostatic Neoplasms - drug therapy Prostatic Neoplasms - mortality Treatment Outcome Tumors Tumors of the urinary system Urinary tract. Prostate gland vitamin D Vitamin D - administration & dosage Vitamin D - adverse effects Vitamin D - blood Vitamin D - therapeutic use |
title | A phase II trial of dexamethasone, vitamin D, and carboplatin in patients with hormone‐refractory prostate cancer |
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