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/m(2) day 1 and B days 1 and 2 (dosage ranging from 50 to 90 mg/m(2)). 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.
Bendamustine and rituximab combination is safe and effective as salvage regimen in Waldenström macroglobulinemia / Tedeschi, A; Picardi, P; Ferrero, S; Benevolo, G; Margiotta Casaluci, G; Varettoni, M; Baratè, C; Motta, M; Gini, G; Goldaniga, Mc; Visco, C; Zaja, Francesco; Belsito Petrizi, V; Ravelli, E; Gentile, M; Urbano, Ma; Franceschetti, S; Ghione, P; Orsucci, L; Frustaci, Am; Gaidano, G; Vitolo, U; Morra, E.. - In: LEUKEMIA & LYMPHOMA. - ISSN 1042-8194. - STAMPA. - 56:9(2015), pp. 2637-2642. [10.3109/10428194.2015.1012714]
Bendamustine and rituximab combination is safe and effective as salvage regimen in Waldenström macroglobulinemia
ZAJA, Francesco;
2015-01-01
Abstract
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/m(2) day 1 and B days 1 and 2 (dosage ranging from 50 to 90 mg/m(2)). 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.| File | Dimensione | Formato | |
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