TY - JOUR
T1 - PBSC mobilization in lymphoma patients
T2 - Analysis of risk factors for collection failure and development of a predictive score based on the kinetics of circulating CD34+ cells and WBC after chemotherapy and G-CSF mobilization
AU - Rossi, Giuseppe
AU - Skert, Cristina
AU - Morello, Enrico
AU - Almici, Camillo
AU - Arcaini, Luca
AU - Basilico, Claudia
AU - Cavalli, Lara
AU - Botto, Barbara
AU - Castelli, Andrea
AU - Pica, Gianmatteo
AU - Ripamonti, Francesco
AU - Salvi, Flavia
AU - Carella, Angelo M.
AU - Gaidano, Gianluca
AU - Levis, Alessandro
AU - Nosari, Annamaria
AU - Russo, Domenico
AU - Vitolo, Umberto
N1 - Publisher Copyright:
© 2015 John Wiley & Sons, Ltd.
PY - 2015/9/1
Y1 - 2015/9/1
N2 - Autologous stem cell transplantation (ASCT) is a potentially curative treatment of lymphoma, but peripheral blood stem cell (PBSC) mobilization fails in some patients. PBSC mobilizing agents have recently been proved to improve the PBSC yield after a prior mobilization failure. Predictive parameters of mobilization failure allowing for a preemptive, more cost-effective use of such agents during the first mobilization attempt are still poorly defined, particularly during mobilization with chemotherapy+granulocyte colony-stimulating factor (G-CSF). We performed a retrospective analysis of a series of lymphoma patients who were candidates for ASCT, to identify factors influencing PBSC mobilization outcome. Premobilization parameters-age, histology, disease status, mobilizing protocol, and previous treatments-as well as white blood cell (WBC) and PBSC kinetics, markers potentially able to predict failure during the ongoing mobilization attempt, were analyzed in 415 consecutive mobilization procedures in 388 patients. We used chemotherapy+G-CSF in 411 (99%) of mobilization attempts and PBSC collection failed (<2×106 CD34+ PBSC/kg) in 13%. Multivariable analysis showed that only a low CD34+ PBSC count and CD34+ PBSC/WBC ratio, together with the use of nonplatinum-containing chemotherapy, independently predicted mobilization failure. Using these three parameters, we established a scoring system to predict risk of failure during mobilization ranging from 2 to 90%, thus allowing a selective use of a preemptive mobilization policy.
AB - Autologous stem cell transplantation (ASCT) is a potentially curative treatment of lymphoma, but peripheral blood stem cell (PBSC) mobilization fails in some patients. PBSC mobilizing agents have recently been proved to improve the PBSC yield after a prior mobilization failure. Predictive parameters of mobilization failure allowing for a preemptive, more cost-effective use of such agents during the first mobilization attempt are still poorly defined, particularly during mobilization with chemotherapy+granulocyte colony-stimulating factor (G-CSF). We performed a retrospective analysis of a series of lymphoma patients who were candidates for ASCT, to identify factors influencing PBSC mobilization outcome. Premobilization parameters-age, histology, disease status, mobilizing protocol, and previous treatments-as well as white blood cell (WBC) and PBSC kinetics, markers potentially able to predict failure during the ongoing mobilization attempt, were analyzed in 415 consecutive mobilization procedures in 388 patients. We used chemotherapy+G-CSF in 411 (99%) of mobilization attempts and PBSC collection failed (<2×106 CD34+ PBSC/kg) in 13%. Multivariable analysis showed that only a low CD34+ PBSC count and CD34+ PBSC/WBC ratio, together with the use of nonplatinum-containing chemotherapy, independently predicted mobilization failure. Using these three parameters, we established a scoring system to predict risk of failure during mobilization ranging from 2 to 90%, thus allowing a selective use of a preemptive mobilization policy.
KW - Autologous stem cell transplantation
KW - Chemotherapy
KW - G-CSF
KW - Lymphoma
KW - Peripheral blood stem cell mobilization
UR - http://www.scopus.com/inward/record.url?scp=84941943956&partnerID=8YFLogxK
U2 - 10.1002/hon.2148
DO - 10.1002/hon.2148
M3 - Article
SN - 0278-0232
VL - 33
SP - 125
EP - 132
JO - Hematological Oncology
JF - Hematological Oncology
IS - 3
ER -