CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS Early consolidation by myeloablative radiochemotherapy followed by autologous stem cell transplantation in first remission significantly prolongs progression-free survival in mantle-cell lymphoma: results of a prospective randomized trial of the European MCL Network

نویسندگان

  • Martin Dreyling
  • Georg Lenz
  • Eva Hoster
  • Achiel Van Hoof
  • Christian Gisselbrecht
  • Rudolf Schmits
  • Bernd Metzner
  • Lorenz Truemper
  • Marcel Reiser
  • Hjalmar Steinhauer
  • Jean-Michel Boiron
  • Marc A. Boogaerts
  • Ali Aldaoud
  • Vittorio Silingardi
  • Hanneke C. Kluin-Nelemans
  • Joerg Hasford
  • Reza Parwaresch
  • Michael Unterhalt
  • Wolfgang Hiddemann
چکیده

Mantle-cell lymphoma (MCL) is characterized by poor prognosis with a median survival of only 3 to 4 years. To improve clinical outcome, the European MCL Network initiated a randomized trial comparing consolidation with myeloablative radiochemotherapy followed by autologous stem cell transplantation (ASCT) to interferon maintenance (IFN ) in first remission. Patients 65 years of age or younger with advanced-stage MCL were assigned to ASCT or IFN after achievement of complete or partial remission by a cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP)–like induction therapy. According to the International Prognostic Index (IPI), 43% of patients had a low-risk, 41% a low-intermediate, 11% a high-intermediate, and 6% a high-risk profile. Sixty-two of 122 patients proceeded to ASCT and 60 received IFN . Patients in the ASCT arm experienced a significantly longer progressionfree survival (PFS) with a median of 39 months compared with 17 months for patients in the IFN arm (P .0108). The 3-year overall survival (OS) was 83% after ASCT versus 77% in the IFN group (P .18). Early consolidation by myeloablative radiochemotherapy followed by ASCT is feasible and results in a significant prolongation of PFS in advancedstage MCL. Longer follow-up is needed to determine the effect on OS. (Blood. 2005; 105:2677-2684)

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تاریخ انتشار 2005