Please use this identifier to cite or link to this item:
https://olympias.lib.uoi.gr/jspui/handle/123456789/23225
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Economopoulos, T. | en |
dc.contributor.author | Psyrri, A. | en |
dc.contributor.author | Dimopoulos, M. A. | en |
dc.contributor.author | Kalogera-Fountzila, A. | en |
dc.contributor.author | Pavlidis, N. | en |
dc.contributor.author | Tsatalas, C. | en |
dc.contributor.author | Nikolaides, C. | en |
dc.contributor.author | Mellou, S. | en |
dc.contributor.author | Xiros, N. | en |
dc.contributor.author | Fountzilas, G. | en |
dc.date.accessioned | 2015-11-24T19:31:12Z | - |
dc.date.available | 2015-11-24T19:31:12Z | - |
dc.identifier.issn | 1528-9117 | - |
dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/23225 | - |
dc.rights | Default Licence | - |
dc.subject | Adolescent | en |
dc.subject | Adult | en |
dc.subject | Aged | en |
dc.subject | Aged, 80 and over | en |
dc.subject | Antibodies, Monoclonal/administration & dosage | en |
dc.subject | Antibodies, Monoclonal, Murine-Derived | en |
dc.subject | Antineoplastic Combined Chemotherapy Protocols/adverse effects/*therapeutic use | en |
dc.subject | Cyclophosphamide/adverse effects/therapeutic use | en |
dc.subject | Epirubicin/adverse effects/therapeutic use | en |
dc.subject | Female | en |
dc.subject | Humans | en |
dc.subject | Lymphoma, B-Cell/drug therapy/pathology | en |
dc.subject | Lymphoma, Mantle-Cell/drug therapy/pathology | en |
dc.subject | Lymphoma, Non-Hodgkin/*drug therapy/pathology | en |
dc.subject | Lymphoma, T-Cell/drug therapy/pathology | en |
dc.subject | Male | en |
dc.subject | Middle Aged | en |
dc.subject | Prednisone/adverse effects/therapeutic use | en |
dc.subject | Vincristine/adverse effects/therapeutic use | en |
dc.title | CEOP-21 versus CEOP-14 chemotherapy with or without rituximab for the first-line treatment of patients with aggressive lymphomas: results of the HE22A99 trial of the Hellenic Cooperative Oncology Group | en |
heal.type | journalArticle | - |
heal.type.en | Journal article | en |
heal.type.el | Άρθρο Περιοδικού | el |
heal.identifier.primary | 10.1097/PPO.0b013e3181570170 | - |
heal.identifier.secondary | http://www.ncbi.nlm.nih.gov/pubmed/17921732 | - |
heal.language | en | - |
heal.access | campus | - |
heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής | el |
heal.publicationDate | 2007 | - |
heal.abstract | BACKGROUND: In this study we investigated whether administering CEOP (cyclophosphamide, epirubicin, vincristine [Oncovin], and prednisone) every 2 weeks (CEOP-14) instead of every 3 weeks (the standard CEOP-21 regimen) improves outcomes in patients with previously untreated aggressive lymphomas. In a secondary analysis we evaluated the impact of adding rituximab to CEOP-14/CEOP-21 chemotherapy. STUDY DESIGN: The trial opened in March 1999, and patients were randomly assigned to either CEOP-14 or CEOP-21. All patients enrolled from May 2002 onward received rituximab with each chemotherapy cycle, and those attaining a complete response received rituximab consolidation. RESULTS: Complete and overall response rates in the CEOP-21 +/- rituximab (N = 114) and CEOP-14 +/- rituximab (N = 103) arms were similar, as were the overall survival (P = 0.769) and time to progression distributions (P = 0.969). Rituximab was shown to have a beneficial effect both on the overall survival and on the time to progression. CONCLUSIONS: Thus far, no significant improvement in outcome has been demonstrated with CEOP-14 +/- rituximab versus CEOP-21 +/- rituximab. However, with addition of rituximab to CEOP-21/CEOP-14, significant improvements in time to progression and overall survival were achieved. | en |
heal.journalName | Cancer J | en |
heal.journalType | peer-reviewed | - |
heal.fullTextAvailability | TRUE | - |
Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ |
Files in This Item:
There are no files associated with this item.
This item is licensed under a Creative Commons License