dc.creatorSantini, G.
dc.creatorDe Souza, C.
dc.creatorAversa, S.
dc.creatorPatti, C.
dc.creatorTedeschi, L.
dc.creatorCandela, M.
dc.creatorOlivieri, A.
dc.creatorChisesi, T.
dc.creatorRubagotti, A.
dc.creatorCenturioni, R.
dc.creatorNardi, V.
dc.creatorCongiu, M.
dc.creatorGennaro, M.
dc.creatorTruini, M.
dc.date2004-05-01
dc.date2014-07-17T15:05:05Z
dc.date2015-11-26T11:25:38Z
dc.date2014-07-17T15:05:05Z
dc.date2015-11-26T11:25:38Z
dc.date.accessioned2018-03-28T20:39:36Z
dc.date.available2018-03-28T20:39:36Z
dc.identifierBrazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 37, n. 5, p. 719-728, 2004.
dc.identifier0100-879X
dc.identifierS0100-879X2004000500014
dc.identifier10.1590/S0100-879X2004000500014
dc.identifierhttp://dx.doi.org/10.1590/S0100-879X2004000500014
dc.identifierhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2004000500014
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/24228
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/24228
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1233390
dc.descriptionThe objective of this multicenter prospective study was to determine the clinical efficacy and toxicity of a polychemotherapeutic third generation regimen, VACOP-B, with or without radiotherapy as front-line therapy in aggressive localized non-Hodgkin's lymphoma. Ninety-three adult patients (47 males and 46 females, median age 45 years) with aggressive localized non-Hodgkin's lymphoma, 43 in stage I and 50 in stage II (non-bulky), were included in the study. Stage I patients received VACOP-B for 6 weeks plus involved field radiotherapy and stage II patients received 12 weeks VACOP-B plus involved field radiotherapy on residual masses. Eighty-six (92.5%) achieved complete remission and 4 (4.3%) partial remission. Three patients (3.2%) were primarily resistant. Ten-year probability of survival, progression-free survival and disease-free survival were 87.3, 79.9 and 83.9%, respectively. Eighty-four patients are surviving at a median observation time of 57 months (range: 6-126). Statistical analysis showed no difference between stages I and II in terms of response, ten-year probability of survival, progression-free survival or disease-free survival. Side effects and toxicity were negligible and were similar in the two patient groups. The results of this prospective study suggest that 6 weeks of VACOP-B treatment plus radiotherapy may be the therapy of choice in stage I aggressive non-Hodgkin's lymphoma. Twelve weeks of VACOP-B treatment with or without radiotherapy was shown to be effective and feasible for stage II. These observations need to be confirmed by a phase III study comparing first and third generation protocols in stage I-II aggressive non-Hodgkin's lymphoma.
dc.description719
dc.description728
dc.languageen
dc.publisherAssociação Brasileira de Divulgação Científica
dc.relationBrazilian Journal of Medical and Biological Research
dc.rightsaberto
dc.sourceSciELO
dc.subjectLocalized aggressive non-Hodgkin's lymphoma
dc.subjectVACOP-B
dc.subjectRadiotherapy
dc.subjectToxicity
dc.titleA third generation regimen VACOP-B with or without adjuvant radiotherapy for aggressive localized non-Hodgkin's lymphoma: report from the Italian Non-Hodgkin's Lymphoma Co-operative Study Group
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución