TY - JOUR
T1 - Bendamustine and rituximab combination is safe and effective as salvage regimen in Waldenström macroglobulinemia
AU - Tedeschi, Alessandra
AU - Picardi, Paola
AU - Ferrero, Simone
AU - Benevolo, Giulia
AU - Margiotta Casaluci, Gloria
AU - Varettoni, Marzia
AU - Baratè, Claudia
AU - Motta, Marina
AU - Gini, Guido
AU - Goldaniga, Maria Cecilia
AU - Visco, Carlo
AU - Zaja, Francesco
AU - Belsito Petrizi, Valeria
AU - Ravelli, Erika
AU - Gentile, Massimo
AU - Urbano, Marina Aurora
AU - Franceschetti, Silvia
AU - Ghione, Paola
AU - Orsucci, Lorella
AU - Frustaci, Anna Maria
AU - Gaidano, Gianluca
AU - Vitolo, Umberto
AU - Morra, Enrica
N1 - Publisher Copyright:
© 2015 Informa UK, Ltd.
PY - 2015/9/2
Y1 - 2015/9/2
N2 - According to the European Society for Medical Oncology and National Comprehensive Cancer Network guidelines on Waldenström macroglobulinemia, bendamustine (B) may be considered a suitable therapeutic option. To address the role of B in combination with rituximab (BR), we analyzed the outcome of 71 patients with relapsed/refractory disease, median age 72 years, treated with R 375 mg/m2 day 1 and B days 1 and 2 (dosage ranging from 50 to 90 mg/m2). Patients had previously received a median number of 2 lines of treatment (range 1-5). Overall and major response rates were 80.2% and 74.6%. Major toxicity was grade 3/4 neutropenia occurring in 13% of courses. There was no significant association between baseline features or patients characteristics and response achievement. Median progression-free survival was not reached after a median follow-up of 19 months (range 3-54). None of the patients developed aggressive lymphoma or secondary myelodysplastic syndrome/acute myeloid leukemia. BR was found to be an active and well-tolerated salvage regimen leading to rapid disease control.
AB - According to the European Society for Medical Oncology and National Comprehensive Cancer Network guidelines on Waldenström macroglobulinemia, bendamustine (B) may be considered a suitable therapeutic option. To address the role of B in combination with rituximab (BR), we analyzed the outcome of 71 patients with relapsed/refractory disease, median age 72 years, treated with R 375 mg/m2 day 1 and B days 1 and 2 (dosage ranging from 50 to 90 mg/m2). Patients had previously received a median number of 2 lines of treatment (range 1-5). Overall and major response rates were 80.2% and 74.6%. Major toxicity was grade 3/4 neutropenia occurring in 13% of courses. There was no significant association between baseline features or patients characteristics and response achievement. Median progression-free survival was not reached after a median follow-up of 19 months (range 3-54). None of the patients developed aggressive lymphoma or secondary myelodysplastic syndrome/acute myeloid leukemia. BR was found to be an active and well-tolerated salvage regimen leading to rapid disease control.
KW - Bendamustine
KW - Waldenström macroglobulinemia
KW - refractory
KW - relapsed
KW - rituximab
KW - salvage
UR - http://www.scopus.com/inward/record.url?scp=84942548240&partnerID=8YFLogxK
U2 - 10.3109/10428194.2015.1012714
DO - 10.3109/10428194.2015.1012714
M3 - Article
SN - 1042-8194
VL - 56
SP - 2637
EP - 2642
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
IS - 9
ER -