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Management of newly diagnosed high‐risk and intermediate‐risk follicular lymphoma with 90 90 Y ibritumomab tiuxetan in a phase II study

机译:在II期研究中,在II期研究中使用90 90 ybritumomab Tiuxetan进行新诊断的高风险和中性风险卵泡淋巴瘤

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Abstract Five‐year overall survival for high‐risk Follicular Lymphoma International Prognostic Index follicular lymphoma is only approximately 50% compared with 90% for low risk. To evaluate an approach to improve upon this poor outcome, we completed an exploratory phase II trial of intensified treatment for patients with intermediate and high‐risk follicular lymphoma. Front‐line treatment with chemo‐immunotherapy consisting of rituximab, cyclophosphamide, vincristine, doxorubicin, and prednisone was followed by radio‐ immunotherapy with 90‐Yttrium ibritumomab tiuxetan consolidation, and 2?years of rituximab maintenance. The 5‐year overall survival for intermediate and high‐risk patients was 88% and 83%, respectively. Of 33 enrolled patients, 3 were off study before receiving radio‐immunotherapy. Three months post radio‐immunotherapy, 28/33 (85%) patients had achieved complete response including 6 patients who had only a partial response to chemo‐immunotherapy and converted to complete response after radio‐immunotherapy. The 5‐year progression‐free survival for intermediate and high risk was 79% and 58%, respectively. Nine of 19 patients with molecular markers patients remain in molecular and clinical complete remission with a median follow‐up of 48?months (range 3‐84?months). Post radio‐immunotherapy, hematologic toxicities were mostly grade 1 and 2. However, asymptomatic grade 3 or 4 thrombocytopenia and neutropenia occurred in 11%‐36% and 10%‐24% of patients, respectively. Myelodysplastic syndrome occurred in 1 patient 4?years post treatment. Whereas many patients had prolonged B‐cell reduction and low immunoglobulin levels post treatment, previous immunities to rubella were maintained. More aggressive upfront approaches such as this may benefit higher risk follicular lymphoma, but confirmatory trials are required. http://www.clinicaltrials.gov : NCT01446562.
机译:摘要五年的高风险卵泡淋巴瘤的整体生存率国际预后指数滤泡淋巴瘤仅为约50%,而低风险为90%。为了评估一种改善这种差的结果的方法,我们完成了探索性期II试验,治疗中间体和高风险淋巴瘤患者的强化治疗。用Rituximab,环膦酰胺,长春新碱,多码霉素和泼尼松组成的化疗免疫疗法进行前线处理,然后用90钇Ibritumomab硫磺酸固结的无线电治疗,以及2年的rituximab维持。中级和高风险患者的5年总生存率分别为88%和83%。在接受无线电免疫疗法之前,33例患者患者,3例休止研究。无线电免疫疗法后三个月,28/33(85%)患者取得了完整的反应,包括6名患者,该患者只对化学免疫疗法进行部分反应并在无线电免疫疗法后转化为完全反应。中间和高风险的5年的无进展生存率分别为79%和58%。 19例分子标记患者的九个患者留在分子和临床完全缓解中,中间有48个月(范围3-84个月)。外无线电疗法后,血液学毒性大多数为1和2.然而,无症状3或4级血小板减少症和中性粒细胞率分别发生在11%-36%和10%-24%的患者中。髓细胞增生综合征发生在1例4岁以下后治疗。然而,许多患者延长了B细胞减少和低免疫球蛋白水平后治疗后,维持先前的免疫力。更具侵略性的前期方法,如这可能会受益于较高的风险滤泡淋巴瘤,但需要确认试验。 http://www.clinicaltrials.gov:nct01446562。

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