Artigo
Immunomodulatory effects of low dose chemotherapy and perspectives of its combination with immunotherapy
Fecha
2013-06-01Registro en:
International Journal of Cancer, v. 132, n. 11, p. 2471-2478, 2013.
0020-7136
1097-0215
10.1002/ijc.27801
WOS:000316824000002
2-s2.0-84875600868
8845835550637809
0000-0002-4292-3298
Autor
Universidade Estadual Paulista (Unesp)
Resumen
Given 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.
Materias
Ítems relacionados
Mostrando ítems relacionados por Título, autor o materia.
-
Association between immunohistochemical expression of topoisomerase II alpha, HER2 and hormone receptors and response to primary chemotherapy in breast cancer
Manna, ED; Teixeira, LC; Alvarenga, M -
Ovarian germ cell cancer: Clinicopathologic analysis and outcome of 31 cases
Kusamura, S; Teixeira, LC; dos Santos, MA; Andrade, LALD; Torres, JCC; Sagarra, A; Deraco, M; Derchain, SFM