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Outcomes of patients with double-hit lymphoma who achieve first complete remission

  • Daniel J. Landsburg
  • , Anthony R. Mato
  • , James N. Gerson
  • , Stefan K. Barta
  • , Marissa K. Falkiewicz
  • , Christina Howlett
  • , Tatyana Feldman
  • , Joseph Maly
  • , Kristie A. Blum
  • , Brian T. Hill
  • , Shaoying Li
  • , L. Jeffrey Medeiros
  • , Pallawi Torka
  • , Francisco Hernandez-Ilizaliturri
  • , Jennifer K. Lue
  • , Jennifer E. Amengual
  • , Nishitha M. Reddy
  • , Arun Singavi
  • , Timothy S. Fenske
  • , Julio C. Chavez
  • Jason B. Kaplan, Amir Behdad, Adam M. Petrich, David J. Peace, Sunita Nathan, Martin A. Bast, Julie M. Vose, Adam J. Olszewski, Cristiana Costa, Frederick Lansigan, Oscar Calzada, Jonathon B. Cohen, Xavier Rivera, Daniel O. Persky, Ryan D. Cassaday
  • University of Pennsylvania
  • Rutgers - The State University of New Jersey, Newark
  • Temple University
  • Rutgers - The State University of New Jersey, New Brunswick
  • Ohio State University
  • Cleveland Clinic Foundation
  • University of Texas MD Anderson Cancer Center
  • Roswell Park Cancer Institute
  • Columbia University
  • Vanderbilt University
  • Medical College of Wisconsin
  • Moffitt Cancer Center
  • Northwestern University
  • AbbVie
  • University of Illinois at Urbana-Champaign
  • Rush University
  • University of Nebraska-Lincoln
  • Brown University
  • Dartmouth College
  • Emory University
  • University of Arizona
  • University of Washington

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

153 Scopus citations

Abstract

Purpose Patients with double-hit lymphoma (DHL) rarely achieve long-term survival following disease relapse. Some patients with DHL undergo consolidative autologous stem-cell transplantation (autoSCT) to reduce the risk of relapse, although the benefit of this treatment strategy is unclear. Methods Patients with DHL who achieved first complete remission following completion of front-line therapy with either rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) or intensive front-line therapy, and deemed fit for autoSCT, were included. A landmark analysis was performed, with time zero defined as 3 months after completion of front-line therapy. Patients who experienced relapse before or who were not followed until that time were excluded. Results Relapse-free survival (RFS) and overall survival (OS) rates at 3 years were 80% and 87%, respectively, for all patients (n = 159). Three-year RFS and OS rates did not differ significantly for autoSCT (n = 62) versus non-autoSCT patients (n = 97), but 3-year RFS was inferior in patients who received R-CHOP compared with intensive therapy (56% v 88%; P = .002). Three-year RFS and OS did not differ significantly for patients in the R-CHOP or intensive therapy cohorts when analyzed by receipt of autoSCT. The median OS following relapse was 8.6 months. Conclusion In the largest reported series, to our knowledge, of patients with DHL to achieve first complete remission, consolidative autoSCT was not associated with improved 3-year RFS or OS. In addition, patients treated with R-CHOP experienced inferior 3-year RFS compared with those who received intensive front-line therapy. When considered in conjunction with reports of patients with newly diagnosed DHL, which demonstrate lower rates of disease response to R-CHOP compared with intensive front-line therapy, our findings further support the use of intensive front-line therapy for this patient population.

Original languageEnglish
Pages (from-to)2260-2267
Number of pages8
JournalJournal of Clinical Oncology
Volume35
Issue number20
DOIs
StatePublished - 10 Jul 2017

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

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