Rituximab added to first-line mitoxantrone, chlorambucil, and prednisolone chemotherapy followed by interferon maintenance prolongs survival in patients with advanced follicular lymphoma:: An East German Study Group hematology and oncology study

被引:403
作者
Herold, Michael
Haas, Antje
Srock, Stefanie
Neser, Sabine
Al-Ali, Kathrin Haifa
Neubauer, Andreas
Doelken, Gottfried
Naumann, Ralph
Knauf, Wolfgang
Freund, Mathias
Rohrberg, Robert
Hoeffken, Klaus
Franke, Astrid
Ittel, Thomas
Kettner, Erika
Haak, Ursula
Mey, Ulrich
Klinkenstein, Christian
Assmann, Michael
von Gruenhagen, Ullrich
机构
[1] HELIOS Klinikum Erfurt GmbH, Med Klin 2, Bereich Hamatol Onkol, D-99089 Erfurt, Germany
[2] Klinikum Ernst von Bergmann, Potsdam, Germany
[3] Free Univ Berlin, Klinikum Rudolf Virchow, Charite, D-1000 Berlin, Germany
[4] Klinikum Chemnitz, Chemnitz, Germany
[5] Univ Leipzig Klinikum, Leipzig, Germany
[6] Univ Marburg Klinikum, Marburg, Germany
[7] Univ Klinikum Greifswald, Greifswald, Germany
[8] Tech Univ Dresden Klinikum, Dresden, Germany
[9] Onkol Schwerpunktpraxis Frankfurt Main, Frankfurt, Germany
[10] Univ Klinikum Rostock, Rostock, Germany
[11] Onkol Schwerpunktpraxis, Halle, Germany
[12] Stadt Krankenhaus Martha Maria Halle Dolau, Halle, Germany
[13] Univ Jena Klinikum, Jena, Germany
[14] Otto von Guericke Univ Klinikum, Magdeburg, Germany
[15] Stadt Klinikum Magdeburg, Magdeburg, Germany
[16] Hansestadt Stralsund GmbH Klinikum, Stralsund, Germany
[17] Univ Bonn Klinikum, Bonn, Germany
[18] Klinikum Frankfurt Oder, Frankfurt, Germany
[19] Krankenhaus Riesa, Riesa, Germany
[20] Onkol Schwerpunktpraxis, Cottbus, Germany
关键词
D O I
10.1200/JCO.2006.06.4618
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Rituximab has been shown to be active in follicular lymphoma (FL), both as monotherapy and in combination with chemotherapy. We conducted a randomized trial comparing mitoxantrone, chlorambucil, and prednisolone (MCP) chemotherapy plus rituximab with MCP alone. Patients and Methods Previously untreated patients with stage III or IV CD20(+) indolent or mantle cell lymphoma were randomly assigned to either eight 28-day cycles of MCP plus rituximab (R-MCP; n = 181) or eight cycles of MCP alone (n = 177). All patients who achieved a complete or partial remission were treated with interferon maintenance until relapse. Herein, we report the results from the primary analysis population of patients with FL, who constituted the majority of patients (56%) recruited to the trial (n = 201; R-MCP, n = 105; MCP, n = 96). Results Rates of overall and complete response were significantly higher in the R-MCP arm than the MCP arm (overall response, 92% v 75%, respectively,- P =.0009; complete response, 50% v 25%, respectively; P =.004). With a median follow-up time of 47 months, median event-free survival (EFS) and progression-free survival (PFS) times were significantly prolonged with R-MCP compared with MCP (EFS, not reached v 26 months, respectively; P <.0001; PFS, not reached v 28.8 months, respectively; P <.0001), and overall survival (OS) was significantly improved with R-MCP compared with MCP (4-year OS rate, 87% v 74%, respectively; P =.0096). Conclusion The R-MCP regimen significantly improves complete and overall response rates, EFS, PFS, and OS in patients with previously untreated advanced FL, without a clinically significant increase in toxicity.
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页码:1986 / 1992
页数:7
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