Standard chemotherapy with interferon compared with CHOP followed by high-dose therapy with autologous stem cell transplantation in untreated patients with advanced follicular lymphoma: the GELF-94 randomized study from the Groupe d'Etude des Lymphomes de l'Adulte (GELA)

  • Catherine Sebban
    From the Departments of Hematology of Centre Léon Bérard, Lyon, France; Hôpital Saint-Louis, Paris, France; Hôpital Necker, Paris, France; Centre Hospitalo-Universitaire (CHU) Henri Mondor, Créteil, France; Centre Becquerel, Rouen, France; CHU de Brabois, Vandoeuvre les Nancy, France; Institut Paoli Calmette, Marseille, France; Université Catholique de Louvain, Yvoir, Belgium; and Hospices Civils de Lyon, Pierre Bénite, France.
  • Nicolas Mounier
    From the Departments of Hematology of Centre Léon Bérard, Lyon, France; Hôpital Saint-Louis, Paris, France; Hôpital Necker, Paris, France; Centre Hospitalo-Universitaire (CHU) Henri Mondor, Créteil, France; Centre Becquerel, Rouen, France; CHU de Brabois, Vandoeuvre les Nancy, France; Institut Paoli Calmette, Marseille, France; Université Catholique de Louvain, Yvoir, Belgium; and Hospices Civils de Lyon, Pierre Bénite, France.
  • Nicole Brousse
    From the Departments of Hematology of Centre Léon Bérard, Lyon, France; Hôpital Saint-Louis, Paris, France; Hôpital Necker, Paris, France; Centre Hospitalo-Universitaire (CHU) Henri Mondor, Créteil, France; Centre Becquerel, Rouen, France; CHU de Brabois, Vandoeuvre les Nancy, France; Institut Paoli Calmette, Marseille, France; Université Catholique de Louvain, Yvoir, Belgium; and Hospices Civils de Lyon, Pierre Bénite, France.
  • Coralie Belanger
    From the Departments of Hematology of Centre Léon Bérard, Lyon, France; Hôpital Saint-Louis, Paris, France; Hôpital Necker, Paris, France; Centre Hospitalo-Universitaire (CHU) Henri Mondor, Créteil, France; Centre Becquerel, Rouen, France; CHU de Brabois, Vandoeuvre les Nancy, France; Institut Paoli Calmette, Marseille, France; Université Catholique de Louvain, Yvoir, Belgium; and Hospices Civils de Lyon, Pierre Bénite, France.
  • Pauline Brice
    From the Departments of Hematology of Centre Léon Bérard, Lyon, France; Hôpital Saint-Louis, Paris, France; Hôpital Necker, Paris, France; Centre Hospitalo-Universitaire (CHU) Henri Mondor, Créteil, France; Centre Becquerel, Rouen, France; CHU de Brabois, Vandoeuvre les Nancy, France; Institut Paoli Calmette, Marseille, France; Université Catholique de Louvain, Yvoir, Belgium; and Hospices Civils de Lyon, Pierre Bénite, France.
  • Corinne Haioun
    From the Departments of Hematology of Centre Léon Bérard, Lyon, France; Hôpital Saint-Louis, Paris, France; Hôpital Necker, Paris, France; Centre Hospitalo-Universitaire (CHU) Henri Mondor, Créteil, France; Centre Becquerel, Rouen, France; CHU de Brabois, Vandoeuvre les Nancy, France; Institut Paoli Calmette, Marseille, France; Université Catholique de Louvain, Yvoir, Belgium; and Hospices Civils de Lyon, Pierre Bénite, France.
  • Herve Tilly
    From the Departments of Hematology of Centre Léon Bérard, Lyon, France; Hôpital Saint-Louis, Paris, France; Hôpital Necker, Paris, France; Centre Hospitalo-Universitaire (CHU) Henri Mondor, Créteil, France; Centre Becquerel, Rouen, France; CHU de Brabois, Vandoeuvre les Nancy, France; Institut Paoli Calmette, Marseille, France; Université Catholique de Louvain, Yvoir, Belgium; and Hospices Civils de Lyon, Pierre Bénite, France.
  • Pierre Feugier
    From the Departments of Hematology of Centre Léon Bérard, Lyon, France; Hôpital Saint-Louis, Paris, France; Hôpital Necker, Paris, France; Centre Hospitalo-Universitaire (CHU) Henri Mondor, Créteil, France; Centre Becquerel, Rouen, France; CHU de Brabois, Vandoeuvre les Nancy, France; Institut Paoli Calmette, Marseille, France; Université Catholique de Louvain, Yvoir, Belgium; and Hospices Civils de Lyon, Pierre Bénite, France.
  • Redah Bouabdallah
    From the Departments of Hematology of Centre Léon Bérard, Lyon, France; Hôpital Saint-Louis, Paris, France; Hôpital Necker, Paris, France; Centre Hospitalo-Universitaire (CHU) Henri Mondor, Créteil, France; Centre Becquerel, Rouen, France; CHU de Brabois, Vandoeuvre les Nancy, France; Institut Paoli Calmette, Marseille, France; Université Catholique de Louvain, Yvoir, Belgium; and Hospices Civils de Lyon, Pierre Bénite, France.
  • Chantal Doyen
    From the Departments of Hematology of Centre Léon Bérard, Lyon, France; Hôpital Saint-Louis, Paris, France; Hôpital Necker, Paris, France; Centre Hospitalo-Universitaire (CHU) Henri Mondor, Créteil, France; Centre Becquerel, Rouen, France; CHU de Brabois, Vandoeuvre les Nancy, France; Institut Paoli Calmette, Marseille, France; Université Catholique de Louvain, Yvoir, Belgium; and Hospices Civils de Lyon, Pierre Bénite, France.
  • Gilles Salles
    From the Departments of Hematology of Centre Léon Bérard, Lyon, France; Hôpital Saint-Louis, Paris, France; Hôpital Necker, Paris, France; Centre Hospitalo-Universitaire (CHU) Henri Mondor, Créteil, France; Centre Becquerel, Rouen, France; CHU de Brabois, Vandoeuvre les Nancy, France; Institut Paoli Calmette, Marseille, France; Université Catholique de Louvain, Yvoir, Belgium; and Hospices Civils de Lyon, Pierre Bénite, France.
  • Bertrand Coiffier
    From the Departments of Hematology of Centre Léon Bérard, Lyon, France; Hôpital Saint-Louis, Paris, France; Hôpital Necker, Paris, France; Centre Hospitalo-Universitaire (CHU) Henri Mondor, Créteil, France; Centre Becquerel, Rouen, France; CHU de Brabois, Vandoeuvre les Nancy, France; Institut Paoli Calmette, Marseille, France; Université Catholique de Louvain, Yvoir, Belgium; and Hospices Civils de Lyon, Pierre Bénite, France.

説明

<jats:title>Abstract</jats:title><jats:p>The purpose of this study is to compare our standard chemotherapy regimen (CHVP [cyclophosphamide, doxorubicin, teniposide, and prednisone]) plus interferon with 4 courses of CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone) followed by high-dose therapy with autologous stem cell transplantation (ASCT) in treatment-naive patients with advanced follicular lymphoma. Four hundred one patients were included from July 1994 to March 2001: 209 received 12 cycles of CHVP plus interferon α for 18 months (CHVP-I arm) and 192 received 4 cycles of CHOP followed by high-dose therapy (HDT) with total body irradiation and ASCT (CHOP-HDT arm). Overall response rates were similar in both groups (79% and 78% after induction chemotherapy, respectively). One hundred thirty-one of the 150 patients eligible for HDT underwent transplantation (87%). Intent-to-treat analysis after a median follow-up of 7.5 years showed that there was no difference between the 2 arms for overall survival (P = .53) or event-free survival (P = .11). Patients with a complete response at the end of the induction therapy had a statistically longer event-free survival and overall survival (P = .02 and < .001, respectively). After long-term follow-up, our study showed that there was no statistically significant benefit in favor of first-line high-dose therapy in patients with follicular lymphoma. High-dose therapy should be reserved for relapsing patients.</jats:p>

収録刊行物

  • Blood

    Blood 108 (8), 2540-2544, 2006-10-15

    American Society of Hematology

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