| Literature DB >> 32782382 |
Carlo Visco1, Alice Di Rocco2, Andrea Evangelista3, Francesca Maria Quaglia4, Maria Chiara Tisi5, Lucia Morello6, Vittorio Ruggero Zilioli7, Chiara Rusconi7,8, Stefan Hohaus9, Roberta Sciarra10, Alessandro Re11, Cristina Tecchio4, Annalisa Chiappella8,12, Ana Marin-Niebla13, Rory McCulloch14, Guido Gini15, Tommasina Perrone16, Luca Nassi17, Elsa Pennese18, Piero Maria Stefani19, Maria Christina Cox20, Valentina Bozzoli21, Alberto Fabbri22, Valentina Polli23, Simone Ferrero24, Maria Isabel Alvarez De Celis25, Antonello Sica26, Luca Petrucci2, Luca Arcaini10, Simon Rule14, Mauro Krampera4, Umberto Vitolo27, Monica Balzarotti6.
Abstract
Patients with mantle cell lymphoma (MCL) that fail induction treatment represent a difficult-to-treat population, where no standard therapy exists. We evaluated outcomes in patients with first relapsed-refractory (r/r) MCL after upfront high dose cytarabine including standard regimens. Overall survival (OS-2) and progression-free survival (PFS-2) were estimated from the time of salvage therapy. The previously described threshold of 24 months was used to define patients as early- or late-progressors (POD). Overall, 261 r/r MCL patients were included. Second-line regimens consisted of rituximab-bendamustine (R-B, 21%), R-B and cytarabine (R-BAC, 29%), ibrutinib (19%), and others (31%). The four groups were balanced in terms of clinicopathological features. Adjusting for age and early/late-POD, patients treated with R-BAC had significantly higher complete remission (63%) than comparators. Overall, Ibrutinib and R-BAC were associated with improved median PFS-2 [24 and 25 months, respectively], compared to R-B (13) or others (7). In patients with early-POD (n = 127), ibrutinib was associated with inferior risk of death than comparators (HR 2.41 for R-B, 2.17 for others, 2.78 for R-BAC). In patients with late-POD (n = 134), no significant differences were observed between ibrutinib and bendamustine-based treatments. Ibrutinib was associated with improved outcome in early-POD patients.Entities:
Mesh:
Year: 2020 PMID: 32782382 DOI: 10.1038/s41375-020-01013-3
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528