TY - JOUR
T1 - Comparison of two initial mobilizing strategies of peripheral blood stem cells for autologous transplantation in patients with lymphoma and human immunodeficiency virus infection
AU - Sagüés, Miguel
AU - Sancho, Juan Manuel
AU - Serrano, David
AU - Balsalobre, Pascual
AU - Gayoso, Jorge
AU - Morgades, Mireia
AU - Conde, Eulogio
AU - Iriondo, Arturo
AU - Varela, Rosario
AU - Escoda, Lourdes
AU - Xicoy, Blanca
AU - Espigado, Ildefonso
AU - Fernández-Abellán, Pascual
AU - Díez, Jose Luis
AU - Ribera, Josep María
PY - 2012/7/21
Y1 - 2012/7/21
N2 - Background and objective: Several studies have demonstrated the feasibility of autologous stem cell transplantation (ASCT) in patients with lymphoma and human immunodeficiency virus (HIV) infection. HIV infection has been described as a risk factor for poor mobilization. The aim of this study was to compare the results of two mobilization strategies of peripheral blood stem cells (PBSC) in patients with lymphoma and HIV infection in seven Spanish hospitals. Patients and methods: The following variables were collected: demographic, clinical and biological features, previous chemotherapies and outcomes, as well as mobilization's strategies (classified in two groups: 1) G-CSF, and 2) G-CSF + chemotherapy). Results: Between January 2000 and May 2010, 42 patients with lymphoma and HIV infection were referred for ASCT. The rate of successful mobilization (collection >1.60 × 10 6 CD34 cells/kg) with the first regimen was 67%, with no differences between those patients mobilized with G-CSF or with G-CSF + chemotherapy (16 [72%] and 12 [60%], respectively; p = 0.382). The status of the lymphoma at the time of mobilization was the only factor for successful mobilization (20/22 patients [91%] in complete remission [CR] mobilized adequately versus 5/12 [58%] in partial remission [PR]; p = 0.038). Conclusions: In patients with lymphoma and HIV infection, mobilization with G-CSF was as effective as mobilization with chemotherapy followed by G-CSF. The stage of disease prior to the mobilization was the main risk factor for the success of mobilization, with better results in patients mobilized in remission of the lymphoma.
AB - Background and objective: Several studies have demonstrated the feasibility of autologous stem cell transplantation (ASCT) in patients with lymphoma and human immunodeficiency virus (HIV) infection. HIV infection has been described as a risk factor for poor mobilization. The aim of this study was to compare the results of two mobilization strategies of peripheral blood stem cells (PBSC) in patients with lymphoma and HIV infection in seven Spanish hospitals. Patients and methods: The following variables were collected: demographic, clinical and biological features, previous chemotherapies and outcomes, as well as mobilization's strategies (classified in two groups: 1) G-CSF, and 2) G-CSF + chemotherapy). Results: Between January 2000 and May 2010, 42 patients with lymphoma and HIV infection were referred for ASCT. The rate of successful mobilization (collection >1.60 × 10 6 CD34 cells/kg) with the first regimen was 67%, with no differences between those patients mobilized with G-CSF or with G-CSF + chemotherapy (16 [72%] and 12 [60%], respectively; p = 0.382). The status of the lymphoma at the time of mobilization was the only factor for successful mobilization (20/22 patients [91%] in complete remission [CR] mobilized adequately versus 5/12 [58%] in partial remission [PR]; p = 0.038). Conclusions: In patients with lymphoma and HIV infection, mobilization with G-CSF was as effective as mobilization with chemotherapy followed by G-CSF. The stage of disease prior to the mobilization was the main risk factor for the success of mobilization, with better results in patients mobilized in remission of the lymphoma.
KW - Chemotherapy
KW - G-CSF
KW - Human immunodeficiency virus
KW - Lymphoma
KW - Mobilization of peripheral blood stem cells
UR - https://www.scopus.com/pages/publications/84862905650
U2 - 10.1016/j.medcli.2011.05.013
DO - 10.1016/j.medcli.2011.05.013
M3 - Article
SN - 0025-7753
VL - 139
SP - 192
EP - 196
JO - Medicina Clinica
JF - Medicina Clinica
IS - 5
ER -