High-dose therapy followed by autologous purged stem cell transplantation and doxorubicin-based chemotherapy in patients with advanced follicular lymphoma: a randomized multicenter study by the GOELAMS with final results after a median follow-up of 9 years

Emmanuel Gyan(Centre Hospitalier Universitaire de Tours), Charles Foussard(Université d'Angers), Philippe B. Bertrand(Université de Tours), Patrick Michenet(Centre hospitalier universitaire d'Orléans), Steven Le Gouill, Christian Berthou(Centre Hospitalier Régional Universitaire de Brest), Hervé Maisonneuve(Roche (Switzerland)), Vincent Delwail, Rémy Gressin(Université Grenoble Alpes), Philippe Quittet(Centre Hospitalier Universitaire de Montpellier), Jean‐Pierre Vilque(Centre François Baclesse), B Desablens(Centre Hospitalier Universitaire Amiens-Picardie), J. Jaubert, Jean‐François Ramée, Nina Arakelyan(Hôpital Européen Georges-Pompidou), Antoine Thyss(Centre Antoine Lacassagne), Cécile Moluçon‐Chabrot, Roselyne Delépine(Centre Hospitalier Universitaire de Tours), Nöel Milpied(Université de Bordeaux), Philippe Colombat(Centre Hospitalier Universitaire de Tours), Éric Deconinck(Inserm)
Blood
October 28, 2008
Cited by 153

Abstract

Autologous stem cell transplantation (ASCT) as first-line therapy for follicular lymphoma (FL) remains controversial. The multicenter study randomized 172 patients with untreated FL for either immunochemotherapy or high-dose therapy (HDT) followed by purged ASCT. Conditioning was performed with total body irradiation (TBI) and cyclophosphamide. The 9-year overall survival (OS) was similar in the HDT and conventional chemotherapy groups (76% and 80%, respectively). The 9-year progression-free survival (PFS) was higher in the ASCT than the chemotherapy group (64% vs 39%; P = .004). A PFS plateau was observed in the HDT group after 7 years. On multivariate analysis, OS and PFS were independently affected by the per-formance status score, the number of nodal areas involved, and the treatment group. Secondary malignancies were more frequent in the HDT than in the chemotherapy group (6 secondary myelodysplastic syndrome/acute myeloid leukemia and 6 second solid tumor cancers vs 1 acute myeloid leukemia, P = .01). The occurrence of a PFS plateau suggests that a subgroup of patients might have their FL cured by ASCT. However, the increased rate of secondary malignancies may discourage the use of purged ASCT in combination with TBI as first-line treatment for FL. This trial has been registered with ClinicalTrials.gov under identifier NCT00696735.


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