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R-CHOP-14 in patients with diffuse large B-cell lymphoma younger than 70 years: a multicentre, prospective study.

机译:年龄小于70岁的弥漫性大B细胞淋巴瘤患者的R-CHOP-14:一项多中心,前瞻性研究。

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Several studies have shown that adding rituximab to CHOP (cyclophosphamide, doxorubicin, vincristine, prednisolone) or reducing the interval between chemotherapy cycles from 3 weeks to 2 weeks improves survival in patients with diffuse large B-cell lymphoma (DLBCL). These studies prompted our group (GOTEL) to evaluate prospectively in a pilot study the feasibility and efficacy of R-CHOP-14 in patients with DLBCL. Patients (<70 years) with stage II bulky or stage III or IV DLBCL and no significant comorbidities were included in the study. Rituximab was administered on day 1 before chemotherapy. R-CHOP was given every 14 days. All patients received filgrastim (5 microg/kg) from days 4 to 10. From May 2002 to August 2004, 80 patients were recruited. Median age was 53 years and 58 patients were <60 years. According to the age-adjusted international prognostic index (aaIPI), 13 patients (16%) had low-risk disease, 31 (39%) low-to-intermediate risk, 27 (34%) high-to-intermediate risk and 9 (11%) high-risk disease. Grade 3-4 neutropenia was observed in 15 patients (17.5%) and grade 3-4 infections in 13 patients (16%). After therapy, 58 patients (73%) achieved CR-CRu (95% CI: 55-90%). With a median follow-up of 26 months, progression-free survival (PFS) and overall survival (OS) at 30 months were 72% and 86%, respectively. Administration of R-CHOP-14 is feasible and effective in patients <70 years.
机译:几项研究表明,将利妥昔单抗添加到CHOP(环磷酰胺,阿霉素,长春新碱,泼尼松龙)或将化疗周期之间的间隔从3周缩短至2周可提高弥散性大B细胞淋巴瘤(DLBCL)患者的生存率。这些研究促使我们的研究小组(GOTEL)在一项初步研究中对R-CHOP-14在DLBCL患者中的可行性和疗效进行了前瞻性评估。 II期大,III期或IV期DLBCL且无明显合并症的患者(<70岁)被纳入研究。利妥昔单抗在化疗前第1天给药。每14天进行一次R-CHOP。从第4天到第10天,所有患者均接受非格司亭(5微克/千克)治疗。从2002年5月至2004年8月,共招募了80例患者。中位年龄为53岁,58名患者<60岁。根据年龄调整后的国际预后指数(aaIPI),低危疾病13例(16%),中低危31例(39%),高中危27例(34%)和9 (11%)高危疾病。在15例患者(17.5%)中观察到3-4级中性粒细胞减少,在13例患者(16%)中观察到3-4级感染。治疗后,有58名患者(73%)达到了CR-CRu(95%CI:55-90%)。中位随访26个月,无进展生存期(PFS)和30个月总生存期(OS)分别为72%和86%。对于70岁以下的患者,R-CHOP-14的给药是可行和有效的。

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