Autologous transplantation as consolidation for high risk aggressive T-cell non-Hodgkin lymphoma: a SWOG 9704 intergroup trial subgroup analysis

  • Zeina Al-Mansour
  • , Hongli Li
  • , James R. Cook
  • , Louis S. Constine
  • , Stephen Couban
  • , Douglas A. Stewart
  • , Thomas C. Shea
  • , Pierluigi Porcu
  • , Jane N. Winter
  • , Brad S. Kahl
  • , Sonali M. Smith
  • , Deborah C. Marcellus
  • , Kevin P. Barton
  • , Glenn M. Mills
  • , Michael LeBlanc
  • , Lisa M. Rimsza
  • , Stephen J. Forman
  • , John P. Leonard
  • , Richard I. Fisher
  • , Jonathan W. Friedberg
  • Patrick J. Stiff

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Phase II data suggest a benefit to autotransplantation for aggressive T-cell non-Hodgkin lymphoma (T-NHL) in first remission; randomized trials have yet to validate this. We performed a retrospective analysis of aggressive T-NHL patients in the intergroup randomized consolidative autotransplant trial (SWOG 9704). Of the 370 enrolled, 40 had T-NHL: 12 were not randomized due to ineligibility (n = 1), choice (n = 2), or progression (n = 9), leaving 13 randomized to control and 15 to autologous stem cell transplantation (ASCT). Two ASCT patients refused transplant and one failed mobilization. The 5-year landmark PFS/OS estimates for ASCT vs. control groups were 40% vs. 38% (p =.56), and 40% vs. 45% (p =.98), respectively. No difference was seen based on IPI, or histologic subtype. Only 1/7 receiving BCNU-based therapy survived vs. 4/5 receiving TBI. Aggressive T-NHL autotransplanted in first remission did not appear to benefit from consolidative ASCT. This and the 30% who dropped out pre-randomization mostly to progression, suggests that improved induction regimens be developed.

Original languageEnglish (US)
Pages (from-to)1934-1941
Number of pages8
JournalLeukemia and Lymphoma
Volume60
Issue number8
DOIs
StatePublished - Jul 3 2019

Keywords

  • T-NHL treatment
  • consolidative autotransplant
  • high-risk T-NHL

ASJC Scopus subject areas

  • Hematology
  • Oncology
  • Cancer Research

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