CHOP-like chemotherapy plus rituximab versus CHOP-like chemotherapy alone in young patients with good-prognosis diffuse large-B-cell lymphoma: a randomised controlled trial by the MabThera International Trial (MInT) Group

The role of rituximab in combination with different CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone)-like chemotherapy regimens in young patients with good-prognosis diffuse large-B-cell lymphoma remains to be defined. We aimed to compare CHOP-like chemotherapy and rituximab with CH...

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Veröffentlicht in:The lancet oncology 2006-05, Vol.7 (5), p.379-391
Hauptverfasser: Pfreundschuh, Michael, Trümper, Lorenz, Österborg, Anders, Pettengell, Ruth, Trneny, Marek, Imrie, Kevin, Ma, David, Gill, Devinder, Walewski, Jan, Zinzani, Pier-Luigi, Stahel, Rolf, Kvaloy, Stein, Shpilberg, Ofer, Jaeger, Ulrich, Hansen, Mads, Lehtinen, Tuula, López-Guillermo, Armando, Corrado, Claudia, Scheliga, Adriana, Milpied, Noel, Mendila, Myriam, Rashford, Michelle, Kuhnt, Evelyn, Loeffler, Markus
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Sprache:eng
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Zusammenfassung:The role of rituximab in combination with different CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone)-like chemotherapy regimens in young patients with good-prognosis diffuse large-B-cell lymphoma remains to be defined. We aimed to compare CHOP-like chemotherapy and rituximab with CHOP-like chemotherapy alone in these patients. 824 patients who were from 18 countries; aged 18–60 years; and who had no risk factors or one risk factor according to age-adjusted International Prognostic Index (IPI), stage II–IV disease, or stage I disease with bulk were enrolled. These patients were randomly assigned to six cycles of CHOP-like chemotherapy and rituximab (n=413) or to six cycles of CHOP-like chemotherapy alone (n=411). Bulky and extranodal sites received additional radiotherapy. The primary endpoint was event-free survival; secondary endpoints were response, progression under therapy, progression-free survival, overall survival, and frequency of toxic effects. Analyses were done by intention to treat and per protocol. This trial is registered at http://www.clinicaltrials.gov, NCT 00064116. After a median follow-up of 34 months (range 0·03–61), patients assigned chemotherapy and rituximab had increased 3-year event-free survival compared with those assigned chemotherapy alone (79% [95% CI 75–83] vs 59% [54–64]; difference between groups 20% [13–27], log-rank p
ISSN:1470-2045
1474-5488
DOI:10.1016/S1470-2045(06)70664-7