TY - JOUR
T1 - Prospective, multicenter randomized GITMO/IIL trial comparing intensive (R-HDS) versus conventional (CHOP-R) chemoimmunotherapy in high-risk follicular lymphoma at diagnosis
T2 - The superior disease control of R-HDS does not translate into an overall survival advantage
AU - Ladetto, Marco
AU - De Marco, Federica
AU - Benedetti, Fabio
AU - Vitolo, Umberto
AU - Parti, Caterina
AU - Rambaldi, Alessandro
AU - Pulsoni, Alessandro
AU - Musso, Maurizio
AU - Liberati, Anna M.
AU - Olivieri, Attilio
AU - Gallamini, Andrea
AU - Pogliani, Enrico
AU - Scalabrini, Delia Rota
AU - Callea, Vincenzo
AU - Raimondo, Francesco Di
AU - Pavone, Vincenzo
AU - Tucci, Alessandra
AU - Cortelazzo, Sergio
AU - Levis, Alessandro
AU - Boccadoro, Mario
AU - Majolino, Ignazio
AU - Pileri, Alessandro
AU - Gianni, Alessandro M.
AU - Passera, Roberto
AU - Corradini, Paolo
AU - Tarella, Corrado
PY - 2008/4/15
Y1 - 2008/4/15
N2 - In this randomized multicenter study of 136 patients, 6 courses of CHOP (cyclophosphamide/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 chemotherapy 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.
AB - In this randomized multicenter study of 136 patients, 6 courses of CHOP (cyclophosphamide/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 chemotherapy 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.
UR - http://www.scopus.com/inward/record.url?scp=43249117980&partnerID=8YFLogxK
U2 - 10.1182/blood-2007-10-116749
DO - 10.1182/blood-2007-10-116749
M3 - Article
C2 - 18239086
AN - SCOPUS:43249117980
SN - 0006-4971
VL - 111
SP - 4004
EP - 4013
JO - Blood
JF - Blood
IS - 8
ER -