Tackling pancreatic cancer with metronomic chemotherapy
Abstract Pancreatic tumours, the majority of which arise from the exocrine pancreas, have recently shown an increasing incidence in western countries. Over the past few years more and more new selective molecules directed against specific cellular targets have become available for cancer therapy, le...
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Veröffentlicht in: | Cancer letters 2017-05, Vol.394, p.88-95 |
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description | Abstract Pancreatic tumours, the majority of which arise from the exocrine pancreas, have recently shown an increasing incidence in western countries. Over the past few years more and more new selective molecules directed against specific cellular targets have become available for cancer therapy, leading to significant improvements. However, despite such advances in therapy, prognosis of pancreatic cancer remains disappointing. Metronomic chemotherapy (MCT), which consists in the administration of continuous, low-dose anticancer drugs, has demonstrated the ability to suppress tumour growth. Thus, it may provide an additional therapeutic opportunity for counteracting the progression of the tumour. Here we discuss evidence arising from preclinical and clinical studies regarding the use of MCT in pancreatic cancer. Good results have generally been achieved in preclinical studies, particularly when MCT was combined with standard dose chemotherapy or antinflammatory, antiangiogenic and immunostimolatory agents. The few available clinical experiences, which mainly refer to retrospective data, have reported good tolerability though mild activity of metronomic schedules. Further studies are therefore awaited to confirm both preclinical findings and the preliminary clinical data. |
doi_str_mv | 10.1016/j.canlet.2017.02.017 |
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Over the past few years more and more new selective molecules directed against specific cellular targets have become available for cancer therapy, leading to significant improvements. However, despite such advances in therapy, prognosis of pancreatic cancer remains disappointing. Metronomic chemotherapy (MCT), which consists in the administration of continuous, low-dose anticancer drugs, has demonstrated the ability to suppress tumour growth. Thus, it may provide an additional therapeutic opportunity for counteracting the progression of the tumour. Here we discuss evidence arising from preclinical and clinical studies regarding the use of MCT in pancreatic cancer. Good results have generally been achieved in preclinical studies, particularly when MCT was combined with standard dose chemotherapy or antinflammatory, antiangiogenic and immunostimolatory agents. The few available clinical experiences, which mainly refer to retrospective data, have reported good tolerability though mild activity of metronomic schedules. Further studies are therefore awaited to confirm both preclinical findings and the preliminary clinical data.</description><identifier>ISSN: 0304-3835</identifier><identifier>EISSN: 1872-7980</identifier><identifier>DOI: 10.1016/j.canlet.2017.02.017</identifier><identifier>PMID: 28232048</identifier><language>eng</language><publisher>Ireland: Elsevier Limited</publisher><subject>Administration, Metronomic ; Angiogenesis ; Animals ; Antiangiogenics ; Antineoplastic Agents - administration & dosage ; Antineoplastic drugs ; Antitumor agents ; Apoptosis - drug effects ; Biomarkers, Tumor - genetics ; Biomarkers, Tumor - metabolism ; Cancer therapies ; Cell Movement - drug effects ; Cell Proliferation - drug effects ; Chemotherapy ; Drug dosages ; Growth factors ; Hematology, Oncology and Palliative Medicine ; Humans ; Incidence ; Kinases ; Neoplasm Metastasis ; Pancreas ; Pancreatic cancer ; Pancreatic Neoplasms - drug therapy ; Pancreatic Neoplasms - genetics ; Pancreatic Neoplasms - metabolism ; Pancreatic Neoplasms - pathology ; Radiation therapy ; Rodents ; Schedules ; Signal Transduction - drug effects ; Studies ; Treatment Outcome ; Tumor Burden - drug effects ; Tumor Microenvironment ; Tumors</subject><ispartof>Cancer letters, 2017-05, Vol.394, p.88-95</ispartof><rights>Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier Limited May 28, 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-edff6ca8b67dc24e2221f3555f8e689eac6763f6b86ba9fdae46fd73a9b0cca73</citedby><cites>FETCH-LOGICAL-c423t-edff6ca8b67dc24e2221f3555f8e689eac6763f6b86ba9fdae46fd73a9b0cca73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28232048$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Romiti, Adriana</creatorcontrib><creatorcontrib>Falcone, Rosa</creatorcontrib><creatorcontrib>Roberto, Michela</creatorcontrib><creatorcontrib>Marchetti, Paolo</creatorcontrib><title>Tackling pancreatic cancer with metronomic chemotherapy</title><title>Cancer letters</title><addtitle>Cancer Lett</addtitle><description>Abstract Pancreatic tumours, the majority of which arise from the exocrine pancreas, have recently shown an increasing incidence in western countries. Over the past few years more and more new selective molecules directed against specific cellular targets have become available for cancer therapy, leading to significant improvements. However, despite such advances in therapy, prognosis of pancreatic cancer remains disappointing. Metronomic chemotherapy (MCT), which consists in the administration of continuous, low-dose anticancer drugs, has demonstrated the ability to suppress tumour growth. Thus, it may provide an additional therapeutic opportunity for counteracting the progression of the tumour. Here we discuss evidence arising from preclinical and clinical studies regarding the use of MCT in pancreatic cancer. Good results have generally been achieved in preclinical studies, particularly when MCT was combined with standard dose chemotherapy or antinflammatory, antiangiogenic and immunostimolatory agents. The few available clinical experiences, which mainly refer to retrospective data, have reported good tolerability though mild activity of metronomic schedules. Further studies are therefore awaited to confirm both preclinical findings and the preliminary clinical data.</description><subject>Administration, Metronomic</subject><subject>Angiogenesis</subject><subject>Animals</subject><subject>Antiangiogenics</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic drugs</subject><subject>Antitumor agents</subject><subject>Apoptosis - drug effects</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Cancer therapies</subject><subject>Cell Movement - drug effects</subject><subject>Cell Proliferation - drug effects</subject><subject>Chemotherapy</subject><subject>Drug dosages</subject><subject>Growth factors</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Incidence</subject><subject>Kinases</subject><subject>Neoplasm Metastasis</subject><subject>Pancreas</subject><subject>Pancreatic cancer</subject><subject>Pancreatic Neoplasms - drug therapy</subject><subject>Pancreatic Neoplasms - genetics</subject><subject>Pancreatic Neoplasms - metabolism</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Radiation therapy</subject><subject>Rodents</subject><subject>Schedules</subject><subject>Signal Transduction - drug effects</subject><subject>Studies</subject><subject>Treatment Outcome</subject><subject>Tumor Burden - drug effects</subject><subject>Tumor Microenvironment</subject><subject>Tumors</subject><issn>0304-3835</issn><issn>1872-7980</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtLJDEURsOgjK0z_0CkwY2bKvN-bAQRXyDMQgdmF1KpG7vaerRJtdL_3hTtA1zN6sLl3EPyfQgdElwSTOTpsvSub2EsKSaqxLTM4weaEa1ooYzGO2iGGeYF00zsof2UlhhjwZX4ifaopoxirmdIPTj_1Db943zleh_BjY2fZ7GHOH9txsW8gzEO_dBN6wV0w7iA6FabX2g3uDbB7_d5gP5eXT5c3BR3f65vL87vCs8pGwuoQ5De6Uqq2lMOlFISmBAiaJDagPNSSRZkpWXlTKgdcBlqxZypsPdOsQN0svWu4vC8hjTarkke2tb1MKyTJVpro4wx_D9QRYUyRIiMHn9Dl8M69vkjk5BTmfPTmeJbyschpQjBrmLTubixBNupA7u02w7s1IHF1OaRz47e5euqg_rz6CP0DJxtAcjBvTQQrc8NNN61T7CB9PUUm7LR3k81Ti1mNyZU_mNv6JmZBA</recordid><startdate>20170528</startdate><enddate>20170528</enddate><creator>Romiti, Adriana</creator><creator>Falcone, Rosa</creator><creator>Roberto, Michela</creator><creator>Marchetti, Paolo</creator><general>Elsevier Limited</general><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>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20170528</creationdate><title>Tackling pancreatic cancer with metronomic chemotherapy</title><author>Romiti, Adriana ; Falcone, Rosa ; Roberto, Michela ; Marchetti, Paolo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-edff6ca8b67dc24e2221f3555f8e689eac6763f6b86ba9fdae46fd73a9b0cca73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Administration, Metronomic</topic><topic>Angiogenesis</topic><topic>Animals</topic><topic>Antiangiogenics</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic drugs</topic><topic>Antitumor agents</topic><topic>Apoptosis - drug effects</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Cancer therapies</topic><topic>Cell Movement - drug effects</topic><topic>Cell Proliferation - drug effects</topic><topic>Chemotherapy</topic><topic>Drug dosages</topic><topic>Growth factors</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Incidence</topic><topic>Kinases</topic><topic>Neoplasm Metastasis</topic><topic>Pancreas</topic><topic>Pancreatic cancer</topic><topic>Pancreatic Neoplasms - drug therapy</topic><topic>Pancreatic Neoplasms - genetics</topic><topic>Pancreatic Neoplasms - metabolism</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Radiation therapy</topic><topic>Rodents</topic><topic>Schedules</topic><topic>Signal Transduction - drug effects</topic><topic>Studies</topic><topic>Treatment Outcome</topic><topic>Tumor Burden - drug effects</topic><topic>Tumor Microenvironment</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Romiti, Adriana</creatorcontrib><creatorcontrib>Falcone, Rosa</creatorcontrib><creatorcontrib>Roberto, Michela</creatorcontrib><creatorcontrib>Marchetti, Paolo</creatorcontrib><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>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Romiti, Adriana</au><au>Falcone, Rosa</au><au>Roberto, Michela</au><au>Marchetti, Paolo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tackling pancreatic cancer with metronomic chemotherapy</atitle><jtitle>Cancer letters</jtitle><addtitle>Cancer Lett</addtitle><date>2017-05-28</date><risdate>2017</risdate><volume>394</volume><spage>88</spage><epage>95</epage><pages>88-95</pages><issn>0304-3835</issn><eissn>1872-7980</eissn><abstract>Abstract Pancreatic tumours, the majority of which arise from the exocrine pancreas, have recently shown an increasing incidence in western countries. Over the past few years more and more new selective molecules directed against specific cellular targets have become available for cancer therapy, leading to significant improvements. However, despite such advances in therapy, prognosis of pancreatic cancer remains disappointing. Metronomic chemotherapy (MCT), which consists in the administration of continuous, low-dose anticancer drugs, has demonstrated the ability to suppress tumour growth. Thus, it may provide an additional therapeutic opportunity for counteracting the progression of the tumour. Here we discuss evidence arising from preclinical and clinical studies regarding the use of MCT in pancreatic cancer. Good results have generally been achieved in preclinical studies, particularly when MCT was combined with standard dose chemotherapy or antinflammatory, antiangiogenic and immunostimolatory agents. The few available clinical experiences, which mainly refer to retrospective data, have reported good tolerability though mild activity of metronomic schedules. Further studies are therefore awaited to confirm both preclinical findings and the preliminary clinical data.</abstract><cop>Ireland</cop><pub>Elsevier Limited</pub><pmid>28232048</pmid><doi>10.1016/j.canlet.2017.02.017</doi><tpages>8</tpages></addata></record> |
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subjects | Administration, Metronomic Angiogenesis Animals Antiangiogenics Antineoplastic Agents - administration & dosage Antineoplastic drugs Antitumor agents Apoptosis - drug effects Biomarkers, Tumor - genetics Biomarkers, Tumor - metabolism Cancer therapies Cell Movement - drug effects Cell Proliferation - drug effects Chemotherapy Drug dosages Growth factors Hematology, Oncology and Palliative Medicine Humans Incidence Kinases Neoplasm Metastasis Pancreas Pancreatic cancer Pancreatic Neoplasms - drug therapy Pancreatic Neoplasms - genetics Pancreatic Neoplasms - metabolism Pancreatic Neoplasms - pathology Radiation therapy Rodents Schedules Signal Transduction - drug effects Studies Treatment Outcome Tumor Burden - drug effects Tumor Microenvironment Tumors |
title | Tackling pancreatic cancer with metronomic chemotherapy |
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