Egyszerű nézet

dc.contributor.author Reményi, Péter
dc.contributor.author Gopcsa L
dc.contributor.author Marton, Imelda
dc.contributor.author Réti, Marienn Györgyi
dc.contributor.author Mikala, Gábor
dc.contributor.author Peto M
dc.contributor.author Barta A
dc.contributor.author Batai A
dc.contributor.author Farkas Z
dc.contributor.author Borbényi, Zita
dc.contributor.author Csukly Z
dc.contributor.author Bodó, Imre
dc.contributor.author Fabian J
dc.contributor.author Kiraly A
dc.contributor.author Lengyel L
dc.contributor.author Piukovics, Klára
dc.contributor.author Torbagyi E
dc.contributor.author Masszi, Tamás
dc.date.accessioned 2015-09-09T08:14:59Z
dc.date.available 2015-09-09T08:14:59Z
dc.date.issued 2014
dc.identifier 84897121067
dc.identifier.citation pagination=451-460; journalVolume=31; journalIssueNumber=4; journalTitle=ADVANCES IN THERAPY;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2058
dc.identifier.uri doi:10.1007/s12325-014-0114-z
dc.description.abstract INTRODUCTION: Biosimilar versions of filgrastim [recombinant human granulocyte colony-stimulating factor (rhG-CSF)] are now widely available. To date, biosimilar rhG-CSF has demonstrated a comparable quality, safety and efficacy profile to the originator product (filgrastim [Neupogen((R))], Amgen Inc., CA, USA) in the prevention and management of neutropenia. Biosimilar rhG-CSFs have also been used to induce peripheral blood stem cell (PBSC) mobilization in patients undergoing autologous stem cell transplantation (AHSCT). The authors have examined the effectiveness of a biosimilar rhG-CSF (Zarzio((R)), Sandoz Biopharmaceuticals, Holzkirchen, Germany) in two retrospective studies across two medical centers in Hungary. METHODS: In Study 1, 70 patients with hematological malignancies scheduled to undergo AHSCT received chemotherapy followed by biosimilar rhG-CSF (2 x 5 mug) for facilitating neutrophil, leukocyte, and platelet engraftment. In study 2, 40 additional patients with lymphoid malignancies and planned AHSCT received chemotherapy followed by biosimilar rhG-CSF for PBSC mobilization. The effectiveness of treatment was assessed by the average yield of cluster of differentiation (CD) 34+ cells and the number of leukaphereses required. RESULTS: In Study 1 (patients undergoing AHSCT), the median age was 56 years and most patients were male (60%). The conditioning regimens were mainly high-dose melphalan (n = 41) and carmustine (BiCNU((R)), Bristol-Myers Squibb, NJ, USA), etoposide, cytarabine and melphalan BEAM (n = 21). Median times to absolute neutrophil and leukocyte engraftment were 9 (range 8-11 days) and 10 (8-12) days, respectively. Median time to platelet engraftment was 10.5 days (7-19 days). In Study 2, the patients' median age was 54 years and the majority (57.5%) were female. The median time interval between day 1 of mobilizing chemotherapy and first leukapheresis was 12 (9-27) days. In the autologous PBSC grafts, the median number of CD34+ cells harvested was 5.2 x 10(6)/kg (2.22-57.07 x 10(6)/kg). The median yield of CD34+ cells per leukapheresis product was 2.47 x 10(6)/kg. In total, 58 leukaphereses were performed in 40 successfully harvested patients. CONCLUSIONS: In line with previous studies with originator rhG-CSF, the findings of this study indicate that biosimilar rhG-CSF following AHSCT is effective and generally well tolerated in the engraftment setting. In addition, biosimilar rhG-CSF is comparable to the originator rhG-CSF in terms of kinetics of PBSC mobilization and yield of CD34+ cells. In conclusion, the authors have demonstrated that the use of biosimilar rhG-CSF is effective and safe in autologous PBSC mobilization and engraftment after AHSCT.
dc.relation.ispartof urn:issn:0741-238X
dc.title Peripheral Blood Stem Cell Mobilization and Engraftment after Autologous Stem Cell Transplantation with Biosimilar rhG-CSF
dc.type Journal Article
dc.date.updated 2015-07-28T11:06:21Z
dc.language.rfc3066 en
dc.identifier.mtmt 2583911
dc.identifier.wos 000335309800006
dc.identifier.pubmed 24687301
dc.contributor.department SE/AOK/K/III. Sz. Belgyógyászati Klinika
dc.contributor.department SZTE/ÁOK/II. sz. Belgyógyászati Klinika és Kardiológiai Központ
dc.contributor.institution Semmelweis Egyetem
dc.contributor.institution Szegedi Tudományegyetem


Kapcsolódó fájlok:

A fájl jelenleg csak egyetemi IP címről érhető el.

Megtekintés/Megnyitás

Ez a rekord az alábbi gyűjteményekben szerepel:

Egyszerű nézet