Anti-tumour activity of platinum compounds in advanced prostate cancer—a systematic literature review
For men with advanced castration-resistant prostate cancer (CRPC), several treatment options are available, including androgen receptor (AR) pathway inhibitors (abiraterone acetate, enzalutamide), taxanes (docetaxel, cabazitaxel) and the radionuclide (radium-223). However, cross-resistance is a clin...
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Veröffentlicht in: | Annals of oncology 2016-06, Vol.27 (6), p.975-984 |
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description | For men with advanced castration-resistant prostate cancer (CRPC), several treatment options are available, including androgen receptor (AR) pathway inhibitors (abiraterone acetate, enzalutamide), taxanes (docetaxel, cabazitaxel) and the radionuclide (radium-223). However, cross-resistance is a clinically relevant problem. Platinum compounds have been tested in a number of clinical trials in molecularly unselected prostate cancer patients. Advances in CRPC molecular profiling have shown that a significant proportion of patients harbour DNA repair defects, which may serve as predictive markers for sensitivity to platinum agents.
To systematically identify and analyse clinical trials that have evaluated platinum agents in advanced prostate cancer patients.
PubMed was searched to identify published clinical trials of platinum agents in advanced prostate cancer. The PRIMSA statement was followed for the systematic review process. Identified trials are analysed for study design, statistical plan, assessments of anti-tumour activity and the potential value of predictive biomarkers.
A total of 163 references were identified by the literature search and 72 publications that met the selection criteria were included in this review; of these 33 used carboplatin, 27 cisplatin, 6 satraplatin, 4 oxaliplatin and 2 other platinum compounds. Overall, anti-tumour activity varies in the range of 10%–40% for objective response and 20%–70% for PSA decline ≥50%. Response seemed highest for the combinations of carboplatin with taxanes or oxaliplatin with gemcitabine. The interpretation of the clinical data is limited by differences in response criteria used and patient populations studied.
Platinum compounds have moderate anti-tumour activity in molecularly unselected patients with advanced prostate cancer. Translational evidence of DNA repair deficiency should be leveraged in future studies to select prostate cancer patients most likely to benefit from platinum-based therapy. |
doi_str_mv | 10.1093/annonc/mdw156 |
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To systematically identify and analyse clinical trials that have evaluated platinum agents in advanced prostate cancer patients.
PubMed was searched to identify published clinical trials of platinum agents in advanced prostate cancer. The PRIMSA statement was followed for the systematic review process. Identified trials are analysed for study design, statistical plan, assessments of anti-tumour activity and the potential value of predictive biomarkers.
A total of 163 references were identified by the literature search and 72 publications that met the selection criteria were included in this review; of these 33 used carboplatin, 27 cisplatin, 6 satraplatin, 4 oxaliplatin and 2 other platinum compounds. Overall, anti-tumour activity varies in the range of 10%–40% for objective response and 20%–70% for PSA decline ≥50%. Response seemed highest for the combinations of carboplatin with taxanes or oxaliplatin with gemcitabine. The interpretation of the clinical data is limited by differences in response criteria used and patient populations studied.
Platinum compounds have moderate anti-tumour activity in molecularly unselected patients with advanced prostate cancer. Translational evidence of DNA repair deficiency should be leveraged in future studies to select prostate cancer patients most likely to benefit from platinum-based therapy.</description><identifier>ISSN: 0923-7534</identifier><identifier>EISSN: 1569-8041</identifier><identifier>DOI: 10.1093/annonc/mdw156</identifier><identifier>PMID: 27052650</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Androgen Receptor Antagonists - adverse effects ; Androgen Receptor Antagonists - therapeutic use ; carboplatin ; castration-resistant prostate cancer ; cisplatin ; Cisplatin - adverse effects ; Cisplatin - therapeutic use ; Clinical Trials as Topic ; Combined Modality Therapy ; Docetaxel ; Humans ; Male ; oxaliplatin ; Phenylthiohydantoin - adverse effects ; Phenylthiohydantoin - analogs & derivatives ; Phenylthiohydantoin - therapeutic use ; platinum ; Platinum Compounds - adverse effects ; Platinum Compounds - therapeutic use ; Prostatic Neoplasms, Castration-Resistant - drug therapy ; Prostatic Neoplasms, Castration-Resistant - pathology ; Prostatic Neoplasms, Castration-Resistant - radiotherapy ; Radium - therapeutic use ; satraplatin ; Taxoids - adverse effects ; Taxoids - therapeutic use ; Treatment Outcome</subject><ispartof>Annals of oncology, 2016-06, Vol.27 (6), p.975-984</ispartof><rights>2016 European Society for Medical Oncology</rights><rights>The Author 2016. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c413t-c28d15327be020704a88012ded564c1524b271a422776242a260518ea65eb0353</citedby><cites>FETCH-LOGICAL-c413t-c28d15327be020704a88012ded564c1524b271a422776242a260518ea65eb0353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27052650$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hager, S.</creatorcontrib><creatorcontrib>Ackermann, C.J.</creatorcontrib><creatorcontrib>Joerger, M.</creatorcontrib><creatorcontrib>Gillessen, S.</creatorcontrib><creatorcontrib>Omlin, A.</creatorcontrib><title>Anti-tumour activity of platinum compounds in advanced prostate cancer—a systematic literature review</title><title>Annals of oncology</title><addtitle>Ann Oncol</addtitle><description>For men with advanced castration-resistant prostate cancer (CRPC), several treatment options are available, including androgen receptor (AR) pathway inhibitors (abiraterone acetate, enzalutamide), taxanes (docetaxel, cabazitaxel) and the radionuclide (radium-223). However, cross-resistance is a clinically relevant problem. Platinum compounds have been tested in a number of clinical trials in molecularly unselected prostate cancer patients. Advances in CRPC molecular profiling have shown that a significant proportion of patients harbour DNA repair defects, which may serve as predictive markers for sensitivity to platinum agents.
To systematically identify and analyse clinical trials that have evaluated platinum agents in advanced prostate cancer patients.
PubMed was searched to identify published clinical trials of platinum agents in advanced prostate cancer. The PRIMSA statement was followed for the systematic review process. Identified trials are analysed for study design, statistical plan, assessments of anti-tumour activity and the potential value of predictive biomarkers.
A total of 163 references were identified by the literature search and 72 publications that met the selection criteria were included in this review; of these 33 used carboplatin, 27 cisplatin, 6 satraplatin, 4 oxaliplatin and 2 other platinum compounds. Overall, anti-tumour activity varies in the range of 10%–40% for objective response and 20%–70% for PSA decline ≥50%. Response seemed highest for the combinations of carboplatin with taxanes or oxaliplatin with gemcitabine. The interpretation of the clinical data is limited by differences in response criteria used and patient populations studied.
Platinum compounds have moderate anti-tumour activity in molecularly unselected patients with advanced prostate cancer. Translational evidence of DNA repair deficiency should be leveraged in future studies to select prostate cancer patients most likely to benefit from platinum-based therapy.</description><subject>Androgen Receptor Antagonists - adverse effects</subject><subject>Androgen Receptor Antagonists - therapeutic use</subject><subject>carboplatin</subject><subject>castration-resistant prostate cancer</subject><subject>cisplatin</subject><subject>Cisplatin - adverse effects</subject><subject>Cisplatin - therapeutic use</subject><subject>Clinical Trials as Topic</subject><subject>Combined Modality Therapy</subject><subject>Docetaxel</subject><subject>Humans</subject><subject>Male</subject><subject>oxaliplatin</subject><subject>Phenylthiohydantoin - adverse effects</subject><subject>Phenylthiohydantoin - analogs & derivatives</subject><subject>Phenylthiohydantoin - therapeutic use</subject><subject>platinum</subject><subject>Platinum Compounds - adverse effects</subject><subject>Platinum Compounds - therapeutic use</subject><subject>Prostatic Neoplasms, Castration-Resistant - drug therapy</subject><subject>Prostatic Neoplasms, Castration-Resistant - pathology</subject><subject>Prostatic Neoplasms, Castration-Resistant - radiotherapy</subject><subject>Radium - therapeutic use</subject><subject>satraplatin</subject><subject>Taxoids - adverse effects</subject><subject>Taxoids - therapeutic use</subject><subject>Treatment Outcome</subject><issn>0923-7534</issn><issn>1569-8041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kLtOxDAQRS0EguVR0iKXNGHHTuwkJUK8JCQaqC2vPYuMEmexnUXb8RF8IV-CVwE6Go8snbmaewg5ZXDBoC3n2vvBm3lv35mQO2SW37ZooGK7ZAYtL4talNUBOYzxFQBky9t9csBrEFwKmJGXS59ckcZ-GAPVJrm1Sxs6LOmq08n5sadm6FfD6G2kzlNt19obtHQVhph0Qmq2__D18alp3MSEfV4ztHMJg05jQBpw7fD9mOwtdRfx5Gcekeeb66eru-Lh8fb-6vKhMBUrU2F4Y5koeb1A4FBDpZsGGLdohawME7xa8JrpivO6lrzimksQrEEtBS6gFOUROZ9y84FvI8akehcNdp32OIxRsQYayZpSthktJtTkLjHgUq2C63XYKAZq61ZNbtXkNvNnP9Hjokf7R__KzEA9AZgL5tJBReNwq8sFNEnZwf0T_Q0ZBYyi</recordid><startdate>20160601</startdate><enddate>20160601</enddate><creator>Hager, S.</creator><creator>Ackermann, C.J.</creator><creator>Joerger, M.</creator><creator>Gillessen, S.</creator><creator>Omlin, A.</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</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>7TO</scope><scope>H94</scope></search><sort><creationdate>20160601</creationdate><title>Anti-tumour activity of platinum compounds in advanced prostate cancer—a systematic literature review</title><author>Hager, S. ; Ackermann, C.J. ; Joerger, M. ; Gillessen, S. ; Omlin, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-c28d15327be020704a88012ded564c1524b271a422776242a260518ea65eb0353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Androgen Receptor Antagonists - adverse effects</topic><topic>Androgen Receptor Antagonists - therapeutic use</topic><topic>carboplatin</topic><topic>castration-resistant prostate cancer</topic><topic>cisplatin</topic><topic>Cisplatin - adverse effects</topic><topic>Cisplatin - therapeutic use</topic><topic>Clinical Trials as Topic</topic><topic>Combined Modality Therapy</topic><topic>Docetaxel</topic><topic>Humans</topic><topic>Male</topic><topic>oxaliplatin</topic><topic>Phenylthiohydantoin - adverse effects</topic><topic>Phenylthiohydantoin - analogs & derivatives</topic><topic>Phenylthiohydantoin - therapeutic use</topic><topic>platinum</topic><topic>Platinum Compounds - adverse effects</topic><topic>Platinum Compounds - therapeutic use</topic><topic>Prostatic Neoplasms, Castration-Resistant - drug therapy</topic><topic>Prostatic Neoplasms, Castration-Resistant - pathology</topic><topic>Prostatic Neoplasms, Castration-Resistant - radiotherapy</topic><topic>Radium - therapeutic use</topic><topic>satraplatin</topic><topic>Taxoids - adverse effects</topic><topic>Taxoids - therapeutic use</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hager, S.</creatorcontrib><creatorcontrib>Ackermann, C.J.</creatorcontrib><creatorcontrib>Joerger, M.</creatorcontrib><creatorcontrib>Gillessen, S.</creatorcontrib><creatorcontrib>Omlin, A.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Annals of oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hager, S.</au><au>Ackermann, C.J.</au><au>Joerger, M.</au><au>Gillessen, S.</au><au>Omlin, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti-tumour activity of platinum compounds in advanced prostate cancer—a systematic literature review</atitle><jtitle>Annals of oncology</jtitle><addtitle>Ann Oncol</addtitle><date>2016-06-01</date><risdate>2016</risdate><volume>27</volume><issue>6</issue><spage>975</spage><epage>984</epage><pages>975-984</pages><issn>0923-7534</issn><eissn>1569-8041</eissn><abstract>For men with advanced castration-resistant prostate cancer (CRPC), several treatment options are available, including androgen receptor (AR) pathway inhibitors (abiraterone acetate, enzalutamide), taxanes (docetaxel, cabazitaxel) and the radionuclide (radium-223). However, cross-resistance is a clinically relevant problem. Platinum compounds have been tested in a number of clinical trials in molecularly unselected prostate cancer patients. Advances in CRPC molecular profiling have shown that a significant proportion of patients harbour DNA repair defects, which may serve as predictive markers for sensitivity to platinum agents.
To systematically identify and analyse clinical trials that have evaluated platinum agents in advanced prostate cancer patients.
PubMed was searched to identify published clinical trials of platinum agents in advanced prostate cancer. The PRIMSA statement was followed for the systematic review process. Identified trials are analysed for study design, statistical plan, assessments of anti-tumour activity and the potential value of predictive biomarkers.
A total of 163 references were identified by the literature search and 72 publications that met the selection criteria were included in this review; of these 33 used carboplatin, 27 cisplatin, 6 satraplatin, 4 oxaliplatin and 2 other platinum compounds. Overall, anti-tumour activity varies in the range of 10%–40% for objective response and 20%–70% for PSA decline ≥50%. Response seemed highest for the combinations of carboplatin with taxanes or oxaliplatin with gemcitabine. The interpretation of the clinical data is limited by differences in response criteria used and patient populations studied.
Platinum compounds have moderate anti-tumour activity in molecularly unselected patients with advanced prostate cancer. Translational evidence of DNA repair deficiency should be leveraged in future studies to select prostate cancer patients most likely to benefit from platinum-based therapy.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>27052650</pmid><doi>10.1093/annonc/mdw156</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Androgen Receptor Antagonists - adverse effects Androgen Receptor Antagonists - therapeutic use carboplatin castration-resistant prostate cancer cisplatin Cisplatin - adverse effects Cisplatin - therapeutic use Clinical Trials as Topic Combined Modality Therapy Docetaxel Humans Male oxaliplatin Phenylthiohydantoin - adverse effects Phenylthiohydantoin - analogs & derivatives Phenylthiohydantoin - therapeutic use platinum Platinum Compounds - adverse effects Platinum Compounds - therapeutic use Prostatic Neoplasms, Castration-Resistant - drug therapy Prostatic Neoplasms, Castration-Resistant - pathology Prostatic Neoplasms, Castration-Resistant - radiotherapy Radium - therapeutic use satraplatin Taxoids - adverse effects Taxoids - therapeutic use Treatment Outcome |
title | Anti-tumour activity of platinum compounds in advanced prostate cancer—a systematic literature review |
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