van Oers Marinus H J, Klasa Richard, Marcus Robert E, Wolf Max, Kimby Eva, Gascoyne Randy D, Jack Andrew, Van't Veer Mars, Vranovsky Andrej, Holte Harald, van Glabbeke Martine, Teodorovic Ivana, Rozewicz Cynthia, Hagenbeek Anton
Department of Hematology F4-224, Academic Medical Center, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands.
Blood. 2006 Nov 15;108(10):3295-301. doi: 10.1182/blood-2006-05-021113. Epub 2006 Jul 27.
We evaluated the role of rituximab (R) both in remission induction and maintenance treatment of relapsed/resistant follicular lymphoma (FL). A total of 465 patients were randomized to induction with 6 cycles of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) (every 3 weeks) or R-CHOP (R: 375 mg/m(2) intravenously, day 1). Those in complete remission (CR) or partial remission (PR) were randomized to maintenance with R (375 mg/m(2) intravenously once every 3 months for a maximum of 2 years) or observation. R-CHOP induction yielded an increased overall response rate (CHOP, 72.3%; R-CHOP, 85.1%; P < .001) and CR rate (CHOP, 15.6%; R-CHOP, 29.5%; P < .001). Median progression-free survival (PFS) from first randomization was 20.2 months after CHOP versus 33.1 months after R-CHOP (hazard ratio [HR], 0.65; P < .001). Rituximab maintenance yielded a median PFS from second randomization of 51.5 months versus 14.9 months with observation (HR, 0.40; P < .001). Improved PFS was found both after induction with CHOP (HR, 0.30; P < .001) and R-CHOP (HR, 0.54; P = .004). R maintenance also improved overall survival from second randomization: 85% at 3 years versus 77% with observation (HR, 0.52; P = .011). This is the first trial showing that in relapsed/resistant FL rituximab maintenance considerably improves PFS not only after CHOP but also after R-CHOP induction.
我们评估了利妥昔单抗(R)在复发/难治性滤泡性淋巴瘤(FL)缓解诱导和维持治疗中的作用。总共465例患者被随机分为接受6个周期的环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)(每3周一次)诱导治疗或R-CHOP(R:375mg/m²静脉注射,第1天)。完全缓解(CR)或部分缓解(PR)的患者被随机分为接受R维持治疗(375mg/m²静脉注射,每3个月一次,最多2年)或观察。R-CHOP诱导治疗使总缓解率提高(CHOP为72.3%;R-CHOP为85.1%;P<.001),CR率提高(CHOP为15.6%;R-CHOP为29.5%;P<.001)。从首次随机分组起,CHOP治疗后的中位无进展生存期(PFS)为20.2个月,而R-CHOP治疗后为33.1个月(风险比[HR],0.65;P<.001)。利妥昔单抗维持治疗从第二次随机分组起的中位PFS为51.5个月,而观察组为14.9个月(HR,0.40;P<.001)。在CHOP诱导治疗后(HR,0.30;P<.001)和R-CHOP诱导治疗后(HR,0.54;P=.004)均发现PFS有所改善。R维持治疗也改善了第二次随机分组后的总生存期:3年时为85%,而观察组为77%(HR,0.52;P=.011)。这是第一项表明在复发/难治性FL中,利妥昔单抗维持治疗不仅在CHOP诱导治疗后,而且在R-CHOP诱导治疗后均能显著改善PFS的试验。