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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/75470
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dc.contributor.authorNars, Mariana S.-
dc.contributor.authorKaneno, Ramon-
dc.date.accessioned2014-05-27T11:29:33Z-
dc.date.accessioned2016-10-25T18:48:42Z-
dc.date.available2014-05-27T11:29:33Z-
dc.date.available2016-10-25T18:48:42Z-
dc.date.issued2013-06-01-
dc.identifierhttp://dx.doi.org/10.1002/ijc.27801-
dc.identifier.citationInternational Journal of Cancer, v. 132, n. 11, p. 2471-2478, 2013.-
dc.identifier.issn0020-7136-
dc.identifier.issn1097-0215-
dc.identifier.urihttp://hdl.handle.net/11449/75470-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/75470-
dc.description.abstractGiven that cancer is one of the main causes of death worldwide, many efforts have been directed toward discovering new treatments and approaches to cure or control this group of diseases. Chemotherapy is the main treatment for cancer; however, a conventional schedule based on maximum tolerated dose (MTD) shows several side effects and frequently allows the development of drug resistance. On the other side, low dose chemotherapy involves antiangiogenic and immunomodulatory processes that help host to fight against tumor cells, with lower grade of side effects. In this review, we present evidence that metronomic chemotherapy, based on the frequent administration of low or intermediate doses of chemotherapeutics, can be better than or as efficient as MTD. Finally, we present some data indicating that noncytotoxic concentrations of antineoplastic agents are able to both up-regulate the immune system and increase the susceptibility of tumor cells to cytotoxic T lymphocytes. Taken together, data from the literature provides us with sufficient evidence that low concentrations of selected chemotherapeutic agents, rather than conventional high doses, should be evaluated in combination with immunotherapy. Copyright © 2012 UICC.en
dc.format.extent2471-2478-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectchemotherapy-
dc.subjectdendritic cells-
dc.subjectimmunotherapy-
dc.subjectmetronomic-
dc.subjectTreg-
dc.subjectvaccine-
dc.subject5 aza 2' deoxycytidine-
dc.subjectadenovirus vector-
dc.subjectantineoplastic agent-
dc.subjectbevacizumab-
dc.subjectcelecoxib-
dc.subjectcetuximab-
dc.subjectcisplatin-
dc.subjectcyclophosphamide-
dc.subjectdendritic cell vaccine-
dc.subjectdocetaxel-
dc.subjectdoxorubicin-
dc.subjectetoposide-
dc.subjectfluorouracil-
dc.subjectfolinic acid-
dc.subjectgemcitabine-
dc.subjectgranulocyte colony stimulating factor-
dc.subjectidarubicin-
dc.subjectinterleukin 12-
dc.subjectirinotecan-
dc.subjectmercaptopurine-
dc.subjectmethotrexate-
dc.subjectmitomycin-
dc.subjectmitoxantrone-
dc.subjectoxaliplatin-
dc.subjectpaclitaxel-
dc.subjectrofecoxib-
dc.subjecttumor cell vaccine-
dc.subjectunindexed drug-
dc.subjectvinblastine-
dc.subjectvincristine-
dc.subjectadvanced cancer-
dc.subjectalopecia-
dc.subjectantiangiogenic activity-
dc.subjectantineoplastic activity-
dc.subjectarthralgia-
dc.subjectbleeding-
dc.subjectblood toxicity-
dc.subjectbone marrow suppression-
dc.subjectbrain damage-
dc.subjectbreast cancer-
dc.subjectbreast metastasis-
dc.subjectcancer chemotherapy-
dc.subjectcancer combination chemotherapy-
dc.subjectcancer immunotherapy-
dc.subjectcancer resistance-
dc.subjectcolon cancer-
dc.subjectcolon carcinoma-
dc.subjectcolorectal cancer-
dc.subjectcytokine response-
dc.subjectcytotoxic T lymphocyte-
dc.subjectdepression-
dc.subjectdigestive system function disorder-
dc.subjectDNA methylation-
dc.subjectdose calculation-
dc.subjectdose response-
dc.subjectdrug cytotoxicity-
dc.subjectdrug megadose-
dc.subjectdrug potentiation-
dc.subjectdrug safety-
dc.subjectdrug sensitivity-
dc.subjectheat injury-
dc.subjectHodgkin disease-
dc.subjecthuman-
dc.subjectimmunological tolerance-
dc.subjectimmunomodulation-
dc.subjectimmunostimulation-
dc.subjectinfection-
dc.subjectleukemia-
dc.subjectleukopenia-
dc.subjectliver toxicity-
dc.subjectlow dose metronomic chemotherapy-
dc.subjectlow drug dose-
dc.subjectlung carcinoma-
dc.subjectlung non small cell cancer-
dc.subjectlymphocytopenia-
dc.subjectlymphoma-
dc.subjectmaintenance therapy-
dc.subjectmalignant neoplastic disease-
dc.subjectmaximum tolerated dose-
dc.subjectmelanoma-
dc.subjectmucosal disease-
dc.subjectmultiple myeloma-
dc.subjectneoplasm-
dc.subjectneuroblastoma-
dc.subjectneutropenia-
dc.subjectnonhuman-
dc.subjectovary cancer-
dc.subjectpriority journal-
dc.subjectreview-
dc.subjectside effect-
dc.subjectsingle drug dose-
dc.subjectstomach tumor-
dc.subjectT cell depletion-
dc.subjectthrombocytopenia-
dc.subjectthromboembolism-
dc.subjectviral gene delivery system-
dc.subjectweight reduction-
dc.subjectAnimals-
dc.subjectAntineoplastic Agents-
dc.subjectCombined Modality Therapy-
dc.subjectHumans-
dc.subjectImmunologic Factors-
dc.subjectImmunotherapy-
dc.subjectNeoplasms-
dc.titleImmunomodulatory effects of low dose chemotherapy and perspectives of its combination with immunotherapyen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartamento de Microbiologia e Imunologia Instituto de Biociências de Botucatu UNESP-Univ Estadual Paulista, Cx Postal 510, Distrito de Rubião Jr. s/n, 18618-970, Botucatu, São Paulo-
dc.description.affiliationDepartment of Pathology School of Medicine UNESP-Univ Estadual Paulista, Botucatu, São Paulo-
dc.description.affiliationUnespDepartamento de Microbiologia e Imunologia Instituto de Biociências de Botucatu UNESP-Univ Estadual Paulista, Cx Postal 510, Distrito de Rubião Jr. s/n, 18618-970, Botucatu, São Paulo-
dc.description.affiliationUnespDepartment of Pathology School of Medicine UNESP-Univ Estadual Paulista, Botucatu, São Paulo-
dc.identifier.doi10.1002/ijc.27801-
dc.identifier.wosWOS:000316824000002-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofInternational Journal of Cancer-
dc.identifier.scopus2-s2.0-84875600868-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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