Prospective, multicenter randomized GITMO/IIL trial comparing intensive (R-HDS) versus conventional (CHOP-R) chemoimmunotherapy in high-risk follicular lymphoma at diagnosis: the superior disease control of R-HDS does not translate into an overall survival advantage

Marco Ladetto(Istituto di Ematologia di Bologna), Federica De Marco(Istituto di Ematologia di Bologna), Fabio Benedetti, Umberto Vitolo(Azienda Ospedaliero Universitaria San Giovanni Battista), Caterina Patti(Ospedale Vincenzo Cervello), Alessandro Rambaldi(Azienda Ospedaliero Universitaria Ospedali Riuniti), Alessandro Pulsoni(Sapienza University of Rome), Maurizio Musso(La Maddalena), Anna Marina Liberati, Attilio Olivieri(Ospedali Riuniti di Ancona), Andrea Gallamini(Azienda Sanitaria Ospedaliera S.Croce e Carle Cuneo), Enrico Pogliani(Azienda Ospedaliera San Gerardo), Delia Rota Scalabrini(Fondazione Piemontese per la Ricerca sul Cancro Onlus), Vincenzo Callea(Azienda ospedaliera "Bianchi-Melacrino-Morelli"), Francesco Di Raimondo(Ferrarotto Hospital), Vincenzo Pavone, Alessandra Tucci(Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia), Sergio Cortelazzo(Ospedale di Bolzano), Alessandro Levis(Azienda Ospedaliera Nazionale SS. Antonio e Biagio e Cesare Arrigo), Mario Boccadoro(Istituto di Ematologia di Bologna), Ignazio Majolino, Alessandro Pileri(Istituto di Ematologia di Bologna), Alessandro M. Gianni, Roberto Passera(Azienda Ospedaliero Universitaria San Giovanni Battista), Paolo Corradini, Corrado Tarella(Istituto di Ematologia di Bologna)
Blood
February 1, 2008
Cited by 253Open Access
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Abstract

Abstract In this randomized multicenter study of 136 patients, 6 courses of CHOP (cyclo-phosphamide/doxorubicin/vincristine/prednisone) followed by rituximab (CHOP-R) were compared with rituximab-supplemented high-dose sequential chemotherapy with autografting (R-HDS) to assess the value of intensified chemo-therapy as a first-line treatment for high-risk follicular lymphoma (FL) after the introduction of monoclonal antibodies. The analysis was intention to treat with event-free survival (EFS) as the primary endpoint. Complete remission (CR) was 62% with CHOP-R and 85% with R-HDS (P < .001). At a median follow-up (MFU) of 51 months, the 4-year EFS was 28% and 61%, respectively (P < .001), with no difference in overall survival (OS). Molecular remission (MR) was achieved in 44% of CHOP-R and 80% of R-HDS patients (P < .001), and was the strongest independent outcome predictor. Patients relapsing after CHOP-R underwent salvage R-HDS in 71% of cases. Salvage R-HDS had an 85% CR rate and a 68% 3-year EFS (MFU, 30 months). We conclude that (1) achieving MR is critical for effective disease control, regardless of which treatment is used; (2) R-HDS ensures superior disease control and molecular outcome than CHOP-R, but no OS improvement; and (3) CHOP-R failures have a good outcome after salvage R-HDS, suggesting that relapsed/refractory FL could be the most appropriate setting for R-HDS–like treatments. This trial was registered at www.clinicaltrials.gov as no. NCT00435955.


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