TY - JOUR
T1 - Randomized trial comparing R-CHOP versus high-dose sequential chemotherapy in high-risk patients with diffuse large B-cell lymphomas
AU - Cortelazzo, Sergio
AU - Tarella, Corrado
AU - Gianni, Alessandro Massimo
AU - Ladetto, Marco
AU - Barbui, Anna Maria
AU - Rossi, Andrea
AU - Gritti, Giuseppe
AU - Corradini, Paolo
AU - Di Nicola, Massimo
AU - Patti, Caterina
AU - Mulé, Antonino
AU - Zanni, Manuela
AU - Zoli, Valerio
AU - Billio, Atto
AU - Piccin, Andrea
AU - Negri, Giovanni
AU - Castellino, Claudia
AU - Di Raimondo, Francesco
AU - Ferreri, Andrés J.M.
AU - Benedetti, Fabio
AU - La Nasa, Giorgio
AU - Gini, Guido
AU - Trentin, Livio
AU - Frezzato, Maurizio
AU - Flenghi, Leonardo
AU - Falorio, Simona
AU - Chilosi, Marco
AU - Bruna, Riccardo
AU - Tabanelli, Valentina
AU - Pileri, Stefano
AU - Masciulli, Arianna
AU - Delaini, Federica
AU - Boschini, Cristina
AU - Rambaldi, Alessandro
N1 - Publisher Copyright:
Copyright © 2016 by American Society of Clinical Oncology. All rights Reserved.
PY - 2016/11/20
Y1 - 2016/11/20
N2 - Purpose The benefit of high-dose chemotherapy with autologous stem-cell transplantation (ASCT) as first-line treatment in patients with diffuse large B-cell lymphomas is still a matter of debate. To address this point, we designed a randomized phase III trial to compare rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP)-14 (eight cycles) with rituximab plus high-dose sequential chemotherapy (R-HDS) with ASCT. Patients and Methods From June 2005 to June 2011, 246 high-risk patients with a high-intermediate (56%) or high (44%) International Prognostic Index score were randomly assigned to the R-CHOP or R-HDS arm, and 235 were analyzed by intent to treat. The primary efficacy end point of the study was 3-year event-free survival, and results were analyzed on an intent-to-treat basis. Results Clinical response (complete response, 78% v 76%; partial response, 5% v 9%) and failures (no response, 15% v 11%; and early treatment-related mortality, 2% v 3%) were similar after R-CHOP versus R-HDS, respectively. After a median follow-up of 5 years, the 3-year event-free survival was 62% versus 65% (P = 83). At 3 years, compared with the R-CHOP arm, the R-HDS arm had better disease-free survival (79% v 91%, respectively; P = .034), but this subsequently vanished because of late-occurring treatment-related deaths. No difference was detected in terms of progression-free survival (65% v 75%, respectively; P = 12), or overall survival (74% v 77%, respectively; P = 64). Significantly higher hematologic toxicity (P<.001) and more infectious complications (P < 001) were observed in the R-HDS arm. Conclusion In this study, front-line intensive R-HDS chemotherapy with ASCT did not improve the outcome of high-risk patients with diffuse large B-cell lymphomas.
AB - Purpose The benefit of high-dose chemotherapy with autologous stem-cell transplantation (ASCT) as first-line treatment in patients with diffuse large B-cell lymphomas is still a matter of debate. To address this point, we designed a randomized phase III trial to compare rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP)-14 (eight cycles) with rituximab plus high-dose sequential chemotherapy (R-HDS) with ASCT. Patients and Methods From June 2005 to June 2011, 246 high-risk patients with a high-intermediate (56%) or high (44%) International Prognostic Index score were randomly assigned to the R-CHOP or R-HDS arm, and 235 were analyzed by intent to treat. The primary efficacy end point of the study was 3-year event-free survival, and results were analyzed on an intent-to-treat basis. Results Clinical response (complete response, 78% v 76%; partial response, 5% v 9%) and failures (no response, 15% v 11%; and early treatment-related mortality, 2% v 3%) were similar after R-CHOP versus R-HDS, respectively. After a median follow-up of 5 years, the 3-year event-free survival was 62% versus 65% (P = 83). At 3 years, compared with the R-CHOP arm, the R-HDS arm had better disease-free survival (79% v 91%, respectively; P = .034), but this subsequently vanished because of late-occurring treatment-related deaths. No difference was detected in terms of progression-free survival (65% v 75%, respectively; P = 12), or overall survival (74% v 77%, respectively; P = 64). Significantly higher hematologic toxicity (P<.001) and more infectious complications (P < 001) were observed in the R-HDS arm. Conclusion In this study, front-line intensive R-HDS chemotherapy with ASCT did not improve the outcome of high-risk patients with diffuse large B-cell lymphomas.
UR - http://www.scopus.com/inward/record.url?scp=84995810071&partnerID=8YFLogxK
U2 - 10.1200/JCO.2016.67.2980
DO - 10.1200/JCO.2016.67.2980
M3 - Article
SN - 0732-183X
VL - 34
SP - 4015
EP - 4022
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 33
ER -