Please use this identifier to cite or link to this item:
http://hdl.handle.net/10553/48523
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Aguiar-Bujanda, David | en_US |
dc.contributor.author | Llorca-Mártinez, Ignacio | en_US |
dc.contributor.author | Rivero-Vera, José C. | en_US |
dc.contributor.author | Blanco-Sánchez, María J. | en_US |
dc.contributor.author | Jiménez-Gallego, Pedro | en_US |
dc.contributor.author | Mori-De Santiago, Marta | en_US |
dc.contributor.author | Limeres-Gonzalez, Miguel A. | en_US |
dc.contributor.author | Cabrera-Marrero, José C. | en_US |
dc.contributor.author | Hernández-Sosa, María | en_US |
dc.contributor.author | Galván-Ruíz, Saray | en_US |
dc.contributor.author | Hernández-Sarmiento, Samuel | en_US |
dc.contributor.author | Saura Grau, Salvador | en_US |
dc.contributor.author | Bohn-Sarmiento, Uriel | en_US |
dc.date.accessioned | 2018-11-23T22:33:14Z | - |
dc.date.available | 2018-11-23T22:33:14Z | - |
dc.date.issued | 2014 | en_US |
dc.identifier.issn | 0278-0232 | en_US |
dc.identifier.uri | http://hdl.handle.net/10553/48523 | - |
dc.description.abstract | There is no standard treatment for patients with gastric marginal zone B-cell lymphoma of the mucosa-associated lymphoid tissue (MALT lymphoma) who are resistant to, or ineligible for, anti-Helicobacter pylori (anti-HP) therapy. In this study, we investigated the activity of the rituximab, cyclophosphamide, vincristine and prednisone (R-CVP) regimen in patients with gastric MALT lymphoma. Patients were included provided they had untreated gastric MALT lymphoma (except for anti-HP therapy) and were resistant to, or ineligible for, anti-HP therapy. Treatment plan consisted of six to eight 21-day cycles of the R-CVP chemotherapy regimen. Toxicity, response, relapse and survival were evaluated. Twenty patients (12 women and 8 men) were included in the analyses with median age of 59 years. Thirteen patients (65%) had stage I tumours, and seven patients (35%) had stages II-IV tumours. The overall response rate was 100%, with 19 (95%) complete responses and one (5%) partial response. Regimen toxicity was mild and mainly hematological, and no cases of gastric bleeding or perforation occurred. After a median follow-up of 56.3 months, three patients had relapsed, and 19 patients remained alive (specific lymphoma survival 100%), of whom 17 had no evidence of disease. In our experience, the R-CVP regimen is a well-tolerated and effective treatment for patients with gastric MALT lymphoma who are resistant to, or ineligible for, anti-HP therapy. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | Hematological Oncology | en_US |
dc.source | Hematological Oncology[ISSN 0278-0232],v. 32, p. 139-144 | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.subject | 320101 Oncología | en_US |
dc.subject.other | Helicobacter pylori | en_US |
dc.subject.other | MALT lymphoma | en_US |
dc.subject.other | Extranodal lymphoma | en_US |
dc.subject.other | Gastric lymphoma | en_US |
dc.subject.other | Marginal zone B-cell lymphoma of the mucosa-associated lymphoid tissue | en_US |
dc.subject.other | Rituximab | en_US |
dc.title | Treatment of gastric marginal zone B-cell lymphoma of the mucosa-associated lymphoid tissue with rituximab, cyclophosphamide, vincristine and prednisone | en_US |
dc.type | info:eu-repo/semantics/article | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1002/hon.2105 | en_US |
dc.identifier.scopus | 84920132387 | - |
dc.contributor.authorscopusid | 55665459800 | - |
dc.contributor.authorscopusid | 22954108200 | - |
dc.contributor.authorscopusid | 6508341920 | - |
dc.contributor.authorscopusid | 57194453426 | - |
dc.contributor.authorscopusid | 55877989400 | - |
dc.contributor.authorscopusid | 55878155500 | - |
dc.contributor.authorscopusid | 6507796809 | - |
dc.contributor.authorscopusid | 55877450700 | - |
dc.contributor.authorscopusid | 55877502800 | - |
dc.contributor.authorscopusid | 55877786400 | - |
dc.contributor.authorscopusid | 55877343200 | - |
dc.contributor.authorscopusid | 35270148700 | - |
dc.contributor.authorscopusid | 6506996382 | - |
dc.description.lastpage | 144 | en_US |
dc.description.firstpage | 139 | en_US |
dc.relation.volume | 32 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
dc.description.numberofpages | 6 | en_US |
dc.utils.revision | Sí | en_US |
dc.date.coverdate | Septiembre 2014 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.sjr | 0,988 | - |
dc.description.jcr | 3,084 | - |
dc.description.sjrq | Q2 | - |
dc.description.jcrq | Q2 | - |
dc.description.scie | SCIE | - |
item.grantfulltext | none | - |
item.fulltext | Sin texto completo | - |
crisitem.author.dept | Departamento de Morfología | - |
crisitem.author.orcid | 0000-0002-6522-7674 | - |
crisitem.author.fullName | Limeres González, Miguel Ángel | - |
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