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首页> 外文期刊>Journal of Clinical Oncology >Phase III randomized intergroup trial of CHOP plus rituximab compared with CHOP chemotherapy plus 131iodine-tositumomab for previously untreated follicular non-hodgkin lymphoma: SWOG S0016
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Phase III randomized intergroup trial of CHOP plus rituximab compared with CHOP chemotherapy plus 131iodine-tositumomab for previously untreated follicular non-hodgkin lymphoma: SWOG S0016

机译:CHOP加利妥昔单抗与CHOP化疗加131碘-tositumomab进行的先前未经治疗的滤泡性非霍奇金淋巴瘤的III期随机对照试验:SWOG S0016

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Purpose: Advanced follicular lymphomas (FL) are considered incurable with conventional chemotherapy and there is no consensus on the best treatment approach. Southwest Oncology Group (SWOG) and Cancer and Leukemia Group B compared the safety and efficacy of two immunochemotherapy regimens for FL in a phase III randomized intergroup protocol (SWOG S0016) that enrolled 554 patients with previously untreated, advanced-stage FL between March 1, 2001, and September 15, 2008 Patients and Methods: Patients were eligible for the study if they had advanced-stage (bulky stage II, III, or IV) evaluable FLof any grade (1, 2, or 3) and had not received previous therapy. In one arm of the study, patients received six cycles of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy at 3-week intervals with six doses of rituximab (CHOP-R). In another arm of the study, patients received six cycles of CHOP followed by consolidation with tositumomab/iodine I-131 tositumomab radioimmunotherapy (RIT). Results: After a median follow-up period of 4.9 years, the 2-year estimate of progression-free survival (PFS) was 76% on the CHOP-R arm and 80% on the CHOP-RIT arm (P =.11). The 2-year estimate of overall survival (OS) was 97% on the CHOP-R arm and 93% on the CHOP-RIT arm (P =.08) Conclusion: There was no evidence of a significant improvement in PFS comparing CHOP-RIT with CHOP-R However, PFS and OS were outstanding on both arms of the study. Future studies are needed to determine the potential benefits of combining CHOP-R induction chemotherapy with RIT consolidation and/or extended rituximab maintenance therapy.
机译:目的:晚期滤泡性淋巴瘤(FL)被认为可通过常规化疗治愈,目前尚无最佳治疗方法的共识。西南肿瘤组(SWOG)与癌症和白血病B组比较了两种免疫化学疗法对FL的安全性和有效性,该方案在III期随机分组间方案(SWOG S0016)中纳入了554例先前未接受治疗的晚期FL患者。 2001年和2008年9月15日,患者和方法:如果患者具有任何级别(1、2或3)的晚期(大型II,III或IV级)可评估FL,则有资格参加研究治疗。在一项研究中,患者每六周接受六次环磷酰胺,阿霉素,长春新碱和泼尼松(CHOP)化疗,共六剂利妥昔单抗(CHOP-R)。在该研究的另一部分中,患者接受CHOP的六个周期,然后接受Tositumomab /碘I-131 Tositumomab放射免疫疗法(RIT)巩固治疗。结果:中位随访期为4.9年后,CHOP-R组的2年无进展生存期(PFS)估计为76%,CHOP-RIT组为80%(P = .11) 。 CHOP-R组的2年总生存期(OS)估计为97%,CHOP-RIT组为93%(P = .08)结论:与CHOP-R组相比,没有证据表明PFS显着改善带有CHOP-R的RIT然而,PFS和OS在研究的两个方面都很出色。需要进一步的研究来确定将CHOP-R诱导化疗与RIT巩固和/或利妥昔单抗维持治疗相结合的潜在益处。

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