首页> 外文OA文献 >Prospective, multicenter randomized GITMO/IIL trial comparing intensive (R-HDS) versus conventional (CHOP-R) chemoimmunotherapy in high-risk follicular lymphoma at diagnosis: the superior disease control of R-HDS does not translate into an overall survival advantage.
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Prospective, multicenter randomized GITMO/IIL trial comparing intensive (R-HDS) versus conventional (CHOP-R) chemoimmunotherapy in high-risk follicular lymphoma at diagnosis: the superior disease control of R-HDS does not translate into an overall survival advantage.

机译:一项前瞻性,多中心的GITMO / IIL随机试验在诊断时对高危滤泡性淋巴瘤的强化(R-HDS)与常规(CHOP-R)化学免疫疗法进行了比较:更好的R-HDS疾病控制不会转化为整体生存优势。

摘要

In this randomized multicenter study of 136 patients, 6 courses of CHOP (cyclophosphamide/ doxorubicin/vincristine/prednisone) followed by rituximab (CHOP-R) were compared with rituximabsupplemented high-dose sequential chemotherapy with autografting (R-HDS) to assess the value of intensified chemotherapy as a first-line treatment for highrisk follicular lymphoma (FL) after the introduction of monoclonal antibodies. The analysis was intention to treat with event-free survival (EFS) as the primary endpoint. Complete remission (CR) was 62% with CHOP-R and 85% with R-HDS (P .001). At a median follow-up (MFU) of 51 months, the 4-year EFS was 28% and 61%, respectively (P .001), with no difference in overall survival (OS). Molecular remission (MR) was achieved in 44% of CHOP-R and 80% of R-HDS patients (P .001), and was the strongest independent outcome predictor. Patients relapsing after CHOP-R underwent salvage R-HDS in 71% of cases. Salvage R-HDS had an 85% CR rate and a 68% 3-year EFS (MFU, 30 months). We conclude that (1) achieving MR is critical for effective disease control, regardless of which treatment is used; (2) R-HDS ensures superior disease control and molecular outcome than CHOP-R, but no OS improvement; and (3) CHOP-R failures have a good outcome after salvage R-HDS, suggesting that relapsed/refractory FL could be the most appropriate setting for R-HDS–like treatments. This trial was registered at www.clinicaltrials.gov as no. NCT00435955.
机译:在这项针对136例患者的随机多中心研究中,将6个疗程的CHOP(环磷酰胺/阿霉素/长春新碱/泼尼松),利妥昔单抗(CHOP-R)与利妥昔单抗联合大剂量顺序化疗加自体移植(R-HDS)进行了比较,以评估其价值。引入单克隆抗体后,强化化疗作为高危滤泡性淋巴瘤(FL)的一线治疗。该分析旨在将无事件生存期(EFS)作为主要终点。 CHOP-R的完全缓解率(CR)为62%,R-HDS的完全缓解率为85%(P 0.001)。在51个月的中位随访(MFU)中,4年EFS分别为28%和61%(P 0.001),总体生存率(OS)没有差异。 44%的CHOP-R患者和80%的R-HDS患者达到了分子缓解(MR)(P 0.001),并且是最强的独立预后指标。在CHOP-R后复发的患者中有71%接受了挽救性R-HDS。抢救性R-HDS的CR率为85%,3年EFS为68%(MFU,30个月)。我们得出的结论是:(1)无论使用哪种治疗方法,实现MR对于有效控制疾病都是至关重要的; (2)与CHOP-R相比,R-HDS可确保更好的疾病控制和分子结果,但OS无改善; (3)挽救R-HDS后CHOP-R失败的预后良好,这表明复发/难治性FL可能是最适合R-HDS疗法的治疗方法。该试验已在www.clinicaltrials.gov上注册为no。 NCT00435955。

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