TY - JOUR
T1 - R-CVP versus R-CHOP versus R-FM for the initial treatment of patients with advanced-stage follicular lymphoma
T2 - Results of the FOLL05 trial conducted by the fondazione italiana linfomi
AU - Federico, Massimo
AU - Luminari, Stefano
AU - Dondi, Alessandra
AU - Tucci, Alessandra
AU - Vitolo, Umberto
AU - Rigacci, Luigi
AU - Raimondo, Francesco Di
AU - Carella, Angelo Michele
AU - Pulsoni, Alessandro
AU - Merli, Francesco
AU - Arcaini, Luca
AU - Angrilli, Francesco
AU - Stelitano, Caterina
AU - Gaidano, Gianluca
AU - Dell'Olio, Matteo
AU - Marcheselli, Luigi
AU - Franco, Vito
AU - Galimberti, Sara
AU - Sacchi, Stefano
AU - Brugiatelli, Maura
PY - 2013/4/20
Y1 - 2013/4/20
N2 - Purpose Although rituximab (R) is commonly used for patients with advanced follicular lymphoma (FL) requiring treatment, the optimal associated chemotherapy regimen has yet to be clarified. Patients and Methods We conducted an open-label, multicenter, randomized trial among adult patients with previously untreated stages II to IV FL to compare efficacy of eight doses of R associated with eight cycles of cyclophosphamide, vincristine, and prednisone (CVP) or six cycles of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) or six cycles of fludarabine and mitoxantrone (FM). The principal end point of the study was time to treatment failure (TTF). Results There were 534 patients enrolled onto the study. Overall response rates were 88%, 93%, and 91% for R-CVP, R-CHOP, and R-FM, respectively (P = .247). After a median follow-up of 34 months, 3-year TTFs were 46%, 62%, and 59% for the respective treatment groups (R-CHOP v R-CVP, P = .003; R-FM v R-CVP, P = .006; R-FM v R-CHOP, P = .763). Three-year progression-free survival (PFS) rates were 52%, 68%, and 63% (overall P = .011), respectively, and 3-year overall survival was 95% for the whole series. R-FM resulted in higher rates of grade 3 to 4 neutropenia (64%) compared with R-CVP (28%) and R-CHOP (50%; P = .001). Overall, 23 second malignancies were registered during follow-up: four in R-CVP, five in R-CHOP, and 14 in R-FM. Conclusion In this study, R-CHOP and R-FM were superior to R-CVP in terms of 3-year TTF and PFS. In addition, R-CHOP had a better risk-benefit ratio compared with R-FM.
AB - Purpose Although rituximab (R) is commonly used for patients with advanced follicular lymphoma (FL) requiring treatment, the optimal associated chemotherapy regimen has yet to be clarified. Patients and Methods We conducted an open-label, multicenter, randomized trial among adult patients with previously untreated stages II to IV FL to compare efficacy of eight doses of R associated with eight cycles of cyclophosphamide, vincristine, and prednisone (CVP) or six cycles of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) or six cycles of fludarabine and mitoxantrone (FM). The principal end point of the study was time to treatment failure (TTF). Results There were 534 patients enrolled onto the study. Overall response rates were 88%, 93%, and 91% for R-CVP, R-CHOP, and R-FM, respectively (P = .247). After a median follow-up of 34 months, 3-year TTFs were 46%, 62%, and 59% for the respective treatment groups (R-CHOP v R-CVP, P = .003; R-FM v R-CVP, P = .006; R-FM v R-CHOP, P = .763). Three-year progression-free survival (PFS) rates were 52%, 68%, and 63% (overall P = .011), respectively, and 3-year overall survival was 95% for the whole series. R-FM resulted in higher rates of grade 3 to 4 neutropenia (64%) compared with R-CVP (28%) and R-CHOP (50%; P = .001). Overall, 23 second malignancies were registered during follow-up: four in R-CVP, five in R-CHOP, and 14 in R-FM. Conclusion In this study, R-CHOP and R-FM were superior to R-CVP in terms of 3-year TTF and PFS. In addition, R-CHOP had a better risk-benefit ratio compared with R-FM.
UR - http://www.scopus.com/inward/record.url?scp=84876578455&partnerID=8YFLogxK
U2 - 10.1200/JCO.2012.45.0866
DO - 10.1200/JCO.2012.45.0866
M3 - Article
SN - 0732-183X
VL - 31
SP - 1506
EP - 1513
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 12
ER -