Identificador persistente para citar o vincular este elemento:
http://hdl.handle.net/10553/43055
Título: | Prediction of normal tissue toxicity as part of the individualized treatment with radiotherapy in oncology patients | Autores/as: | Henríquez-Hernández, Luis Alberto Bordón, Elisa Pinar, Beatriz Lloret, Marta Rodríguez-Gallego, Carlos Lara, Pedro C. |
Palabras clave: | Breast-Cancer Patients Peripheral-Blood Lymphocytes Radiation-Induced Apoptosis Human Skin Fibroblasts Hyperfractionated Radical Radiotherapy, et al. |
Fecha de publicación: | 2012 | Editor/a: | 0960-7404 | Publicación seriada: | Surgical Oncology | Resumen: | Normal tissue toxicity caused by radiotherapy conditions the success of the treatment and the quality of life of patients. Radiotherapy is combined with surgery in both the preoperative or postoperative setting for the treatment of most localized solid tumour types. Furthermore, radical radiotherapy is an alternative to surgery in several tumour locations. The possibility of predicting such radiation-induced toxicity would make possible a better treatment schedule for the individual patient. Radiation-induced toxicity is, at least in part, genetically determined. From decades, several predictive tests have been proposed to know the individual sensitivity of patients to the radiotherapy schedules. Among them, initial DNA damage, radiation-induced apoptosis, gene expression profiles, and gene polymorphisms have been proposed. We report here an overview of the main studies regarding to this field. Radiation-induced apoptosis in peripheral blood lymphocytes seem to be the most promising assay tested in prospective clinical trials, although they have to be validated in large clinical studies. Other promising assays, as those related with single nucleotide polymorphisms, need to be validated as well. (C) 2011 Elsevier Ltd. All rights reserved. | URI: | http://hdl.handle.net/10553/43055 | ISSN: | 0960-7404 | DOI: | 10.1016/j.suronc.2011.12.002 | Fuente: | Surgical Oncology[ISSN 0960-7404],v. 21, p. 201-206 |
Colección: | Reseña |
Citas SCOPUSTM
29
actualizado el 17-nov-2024
Citas de WEB OF SCIENCETM
Citations
26
actualizado el 17-nov-2024
Visitas
76
actualizado el 06-jul-2024
Google ScholarTM
Verifica
Altmetric
Comparte
Exporta metadatos
Los elementos en ULPGC accedaCRIS están protegidos por derechos de autor con todos los derechos reservados, a menos que se indique lo contrario.