Background: Patients with relapsed or refractory classical Hodgkin lymphoma (R/R cHL) have limited opportunities for curative therapy. High-dose therapy followed by autologous stem cell transplantation (HDT-ASCT) produces cure rates of 50% to 60%. Patients relapsing after, or ineligible for HDT-ASCT have limited therapeutic options and long-term remission is uncommon. Furthermore, few patients are candidate to allogeneic stem cell transplantation (AlSCT), a potentially curative approach. The combination of brentuximab vedotin and bendamustine (BVB) is a promising treatment for patients with R/R cHL, regardless of SCT eligibility. Patients and methods: We conducted a real-life study of BVB in 41 patients with R/R cHL after failure of >= 1 therapy including ASCT, AlSCT, or BV. Results: Among 40 patients evaluable for efficacy, the overall response rate and complete response (CR) rate were 75% and 50%, respectively. No significant differences were observed between patients with primary refractory and relapsed disease, previously treated with <= 2 and >= 3 lines of therapy, or BV-exposed and BV-naive. After a median follow-up of 38 months, the median progression free survival (PFS) for the entire population is 26 months; PFS is not reached, 10.5 months, and 4 months for patients achieving CR, partial response and no response, respectively (P < .0001). BVB was well tolerated and no grade 4 toxicity or new safety signals were observed. The most common treatment-emergent adverse events were infections. Conclusion: Our experience supports the efficacy and tolerability of the BVB combination in R/R cHL as a bridge to SCT, or as a definitive therapy for SCT-ineligible patients. Larger comparative studies testing BVB against standards of care are warranted in both settings. (C) 2021 The Authors. Published by Elsevier Inc.

Brentuximab Vedotin and Bendamustine Produce Long-Term Clinical Benefit in Patients With Relapsed or Refractory Classical Hodgkin Lymphoma: A Multicenter Real-Life Experience / Moretti, Marina; Liberati, Anna Marina; Rigacci, Luigi; Puccini, Benedetta; Pulsoni, Alessandro; Gini, Guido; Galieni, Piero; Fabbri, Alberto; Cantonetti, Maria; Pavone, Vincenzo; Bolis, Silvia; Botto, Barbara; Renzi, Daniela; Falchi, Lorenzo. - In: CLINICAL LYMPHOMA MYELOMA & LEUKEMIA. - ISSN 2152-2650. - 22:3(2022), pp. 198-204. [10.1016/j.clml.2021.09.018]

Brentuximab Vedotin and Bendamustine Produce Long-Term Clinical Benefit in Patients With Relapsed or Refractory Classical Hodgkin Lymphoma: A Multicenter Real-Life Experience

Pulsoni, Alessandro;
2022

Abstract

Background: Patients with relapsed or refractory classical Hodgkin lymphoma (R/R cHL) have limited opportunities for curative therapy. High-dose therapy followed by autologous stem cell transplantation (HDT-ASCT) produces cure rates of 50% to 60%. Patients relapsing after, or ineligible for HDT-ASCT have limited therapeutic options and long-term remission is uncommon. Furthermore, few patients are candidate to allogeneic stem cell transplantation (AlSCT), a potentially curative approach. The combination of brentuximab vedotin and bendamustine (BVB) is a promising treatment for patients with R/R cHL, regardless of SCT eligibility. Patients and methods: We conducted a real-life study of BVB in 41 patients with R/R cHL after failure of >= 1 therapy including ASCT, AlSCT, or BV. Results: Among 40 patients evaluable for efficacy, the overall response rate and complete response (CR) rate were 75% and 50%, respectively. No significant differences were observed between patients with primary refractory and relapsed disease, previously treated with <= 2 and >= 3 lines of therapy, or BV-exposed and BV-naive. After a median follow-up of 38 months, the median progression free survival (PFS) for the entire population is 26 months; PFS is not reached, 10.5 months, and 4 months for patients achieving CR, partial response and no response, respectively (P < .0001). BVB was well tolerated and no grade 4 toxicity or new safety signals were observed. The most common treatment-emergent adverse events were infections. Conclusion: Our experience supports the efficacy and tolerability of the BVB combination in R/R cHL as a bridge to SCT, or as a definitive therapy for SCT-ineligible patients. Larger comparative studies testing BVB against standards of care are warranted in both settings. (C) 2021 The Authors. Published by Elsevier Inc.
2022
Bendamustine; Brentuximab; Hodgkin lymphoma; Stem Cell Transplantation
01 Pubblicazione su rivista::01a Articolo in rivista
Brentuximab Vedotin and Bendamustine Produce Long-Term Clinical Benefit in Patients With Relapsed or Refractory Classical Hodgkin Lymphoma: A Multicenter Real-Life Experience / Moretti, Marina; Liberati, Anna Marina; Rigacci, Luigi; Puccini, Benedetta; Pulsoni, Alessandro; Gini, Guido; Galieni, Piero; Fabbri, Alberto; Cantonetti, Maria; Pavone, Vincenzo; Bolis, Silvia; Botto, Barbara; Renzi, Daniela; Falchi, Lorenzo. - In: CLINICAL LYMPHOMA MYELOMA & LEUKEMIA. - ISSN 2152-2650. - 22:3(2022), pp. 198-204. [10.1016/j.clml.2021.09.018]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1706417
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