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Phase 2 trial of bortezomib in combination with rituximab plus hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone alternating with bortezomib, rituximab, methotrexate, and cytarabine for untreated mantle cell lymphoma

  • Jorge E. Romaguera
  • , Michael Wang
  • , Lei Feng
  • , Luis E. Fayad
  • , Frederick Hagemeister
  • , Peter McLaughlin
  • , M. Alma Rodriguez
  • , Michelle Fanale
  • , Robert Orlowski
  • , Larry W. Kwak
  • , Sattva Neelapu
  • , Yasuhiro Oki
  • , Barbara Pro
  • , Anas Younes
  • , Felipe Samaniego
  • , Nathan Fowler
  • , Kimberly Hartig
  • , Marisa Valentinetti
  • , Judy Smith
  • , Peggy Ford
  • Adam Naig, L. Jeffrey Medeiros, Hagop M. Kantarjian, Andre Goy
  • University of Texas MD Anderson Cancer Center
  • City of Hope National Med Center
  • Memorial Sloan-Kettering Cancer Center
  • Rutgers - The State University of New Jersey, Newark

Research output: Contribution to journal › Article › peer-review

14 Scopus citations

Abstract

BACKGROUND: Although the outcomes of patients with mantle cell lymphoma (MCL) have improved, there is still no cure. Bortezomib has a 33% response rate in relapsed/refractory MCL and has shown additive and/or synergistic effects in preclinical trials with known effective agents. METHODS: This is a report of a prospective phase 2 trial of bortezomib added to rituximab plus hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone (BzR-hyperCVAD)/rituximab, high-dose methotrexate, and high-dose cytarabine (BzR-MA) for 95 patients with newly diagnosed MCL. RESULTS: The overall and complete response rates were 100% and 82%, respectively. Hematologic toxicity was high but expected and did not lead to an increased incidence of neutropenic fever or dose reductions in comparison with a similar reported regimen without bortezomib. After a median follow-up of 44 months, the median overall survival had not been reached, and the time to treatment failure (TTF) was 55 months, which is not different from that of historical controls. CONCLUSIONS: BzR-hyperCVAD/BzR-MA at the dose and schedule studied produced high rates of response and a TTF similar to that of historical reports without bortezomib. Cancer 2018;124:2561-9.

Original languageEnglish
Pages (from-to)2561-2569
Number of pages9
JournalCancer
Volume124
Issue number12
DOIs
StatePublished - 15 Jun 2018

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

Keywords

  • and dexamethasone (R-hyperCVAD)
  • bortezomib
  • doxorubicin
  • mantle cell lymphoma
  • rituximab plus hyperfractionated cyclophosphamide
  • vincristine

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