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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Veröffentlicht in:Cancer 2006-07, Vol.107 (2), p.266-274
Hauptverfasser: Flaig, Thomas W., Barqawi, Albaha, Miller, Gary, Kane, Madeleine, Zeng, Chan, Crawford, E. David, Glodé, L. Michael
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container_end_page 274
container_issue 2
container_start_page 266
container_title Cancer
container_volume 107
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
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David ; Glodé, L. Michael</creator><creatorcontrib>Flaig, Thomas W. ; Barqawi, Albaha ; Miller, Gary ; Kane, Madeleine ; Zeng, Chan ; Crawford, E. David ; Glodé, L. Michael</creatorcontrib><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><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 &amp; dosage ; Carboplatin - adverse effects ; Carboplatin - therapeutic use ; dexamethasone ; Dexamethasone - administration &amp; 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. 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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. 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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 &amp; 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. 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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 &amp; dosage</topic><topic>Carboplatin - adverse effects</topic><topic>Carboplatin - therapeutic use</topic><topic>dexamethasone</topic><topic>Dexamethasone - administration &amp; 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 &amp; 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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source Wiley Free Content; Wiley Online Library - AutoHoldings Journals; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
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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