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Outcomes in first relapsed-refractory younger patients with mantle cell lymphoma: results from the MANTLE-FIRST study

  • Carlo Visco*
  • , Alice Di Rocco
  • , Andrea Evangelista
  • , Francesca Maria Quaglia
  • , Maria Chiara Tisi
  • , Lucia Morello
  • , Vittorio Ruggero Zilioli
  • , Chiara Rusconi
  • , Stefan Hohaus
  • , Roberta Sciarra
  • , Alessandro Re
  • , Cristina Tecchio
  • , Annalisa Chiappella
  • , Ana Marin-Niebla
  • , Rory McCulloch
  • , Guido Gini
  • , Tommasina Perrone
  • , Luca Nassi
  • , Elsa Pennese
  • , Piero Maria Stefani
  • Maria Christina Cox, Valentina Bozzoli, Alberto Fabbri, Valentina Polli, Simone Ferrero, Maria Isabel Alvarez De Celis, Antonello Sica, Luca Petrucci, Luca Arcaini, Simon Rule, Mauro Krampera, Umberto Vitolo, Monica Balzarotti
*Corresponding author for this work
  • University of Verona
  • University of Rome La Sapienza
  • Azienda Ospedaliera - Universitaria Città della Salute e della Scienza di Torino
  • Azienda Sanitaria Ulss 6 Vicenza
  • IRCCS Istituto Clinico Humanitas - Rozzano (Milano)
  • Niguarda Hospital
  • IRCCS Fondazione Istituto Nazionale per lo studio e la cura dei tumori - Milano
  • Fondazione Policlinico Universitario A. Gemelli IRCCS
  • IRCCS Fondazione Policlinico San Matteo - Pavia
  • Brescia Civil Hospital
  • Hematology Department
  • University of Plymouth
  • Marche Polytechnic University
  • University of Bari
  • Azienda Ospedaliero-Universitaria Maggiore della Carità
  • Hematology
  • General Hospital Ca’ Foncello
  • Hematology
  • Hematology
  • Azienda Ospedaliera Universitaria Senese
  • Ospedale degli Infermi
  • Azienda Ospedaliera Santa Maria Nuova di Reggio Emilia
  • Hematology Unit
  • Candiolo Cancer Institute

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish
Pages (from-to)787-795
Number of pages9
JournalLeukemia
Volume35
Issue number3
DOIs
Publication statusPublished - Mar 2021

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

ASJC Scopus subject areas

  • Hematology
  • Oncology
  • Cancer Research

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