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R-CHOP 14 with or without radiotherapy in nonbulky limited-stage diffuse large B-cell lymphoma

机译:非肿块有限期弥漫性大B细胞淋巴瘤伴或不伴放疗的R-CHOP 14

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摘要

The benefit of radiotherapy (RT) after chemotherapy in limited-stage diffuse large B-cell lymphoma (DLBCL) remains controversial. We conducted a randomized trial in patients with nonbulky limited-stage DLBCL to evaluate the benefit of RT after rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP). Patients were stratified according to the modified International Prognostic Index, including lactate dehydrogenase, Eastern Cooperative Oncology Group performance status, age, and disease stage. The patients received 4 or 6 consecutive cycles of R-CHOP delivered once every 2 weeks, followed or not by RT at 40 Gy delivered 4 weeks after the last R-CHOP cycle. All patients were evaluated by fluorodeoxyglucose-positron emission tomography scans performed at baseline, after 4 cycles of R-CHOP, and at the end of treatment. The primary objective of the trial was event-free survival (EFS) from randomization. The trial randomly assigned 165 patients in the R-CHOP arm and 169 in the R-CHOP plus RT arm. In an intent-to-treat analysis with a median follow-up of 64 months, 5-year EFS was not statistically significantly different between the 2 arms, with 89% ± 2.9% in the R-CHOP arm vs 92% ± 2.4% in the R-CHOP plus RT arm (hazard ratio, 0.61; 95% confidence interval [CI], 0.3-1.2; P = .18). Overall survival was also not different at 92% (95% CI, 89.5%-94.5%) for patients assigned to R-CHOP alone and 96% (95% CI, 94.3%-97.7%) for those assigned to R-CHOP plus RT (P = not significant). R-CHOP alone is not inferior to R-CHOP followed by RT in patients with nonbulky limited-stage DLBCL. This trial was registered at as #.
机译:有限期弥漫性大B细胞淋巴瘤(DLBCL)化疗后放疗(RT)的益处仍存在争议。我们对非大容量有限期DLBCL患者进行了一项随机试验,以评估利妥昔单抗加环磷酰胺,阿霉素,长春新碱和泼尼松(R-CHOP)后接受RT的益处。根据修改后的国际预后指数对患者进行分层,包括乳酸脱氢酶,东部合作肿瘤小组的表现状况,年龄和疾病阶段。患者每2周接受一次连续的4或6个R-CHOP循环,最后一次R-CHOP循环后4周以40 Gy的RT接受或不接受RT。在基线,R-CHOP 4周期后和治疗结束时,通过氟脱氧葡萄糖-正电子发射断层扫描对所有患者进行了评估。该试验的主要目的是通过随机分组进行无事件生存(EFS)。该试验随机分配了R-CHOP组的165名患者和R-CHOP加RT组的169名患者。在意向性治疗分析中位数为64个月的随访中,两组之间的5年EFS在统计学上没有显着差异,R-CHOP组为89%±2.9%,而92%±2.4%在R-CHOP和RT组中(危险比为0.61; 95%置信区间[CI]为0.3-1.2; P = 0.18)。单独接受R-CHOP的患者的总生存率也没有差异,分别为92%(95%CI,89.5%-94.5%)和接受R-CHOP plus的患者为96%(95%CI,94.3%-97.7%) RT(P =不重要)。对于非大容量有限期DLBCL患者,仅R-CHOP并不比R-CHOP其次是RT低。该试用版注册为#。

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