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
Hauptverfasser: Romiti, Adriana, Falcone, Rosa, Roberto, Michela, Marchetti, Paolo
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container_title Cancer letters
container_volume 394
creator Romiti, Adriana
Falcone, Rosa
Roberto, Michela
Marchetti, Paolo
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.
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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. 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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><subject>Administration, Metronomic</subject><subject>Angiogenesis</subject><subject>Animals</subject><subject>Antiangiogenics</subject><subject>Antineoplastic Agents - administration &amp; 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 ; 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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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