首页> 外文期刊>Journal of Clinical Oncology >Cyclophosphamide, vincristine, and prednisone followed by tositumomab and iodine-131-tositumomab in patients with untreated low-grade follicular lymphoma: eight-year follow-up of a multicenter phase II study.
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Cyclophosphamide, vincristine, and prednisone followed by tositumomab and iodine-131-tositumomab in patients with untreated low-grade follicular lymphoma: eight-year follow-up of a multicenter phase II study.

机译:未经治疗的低度滤泡性淋巴瘤患者应使用环磷酰胺,长春新碱和泼尼松,继而接受tositumomab和碘131-tositumomab治疗:一项多中心II期研究的八年随访。

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PURPOSE: The efficacy and safety of cyclophosphamide, vincristine, and prednisone (CVP) followed by tositumomab and iodine-131 ((131)I) -tositumomab therapy were evaluated in a multicenter phase II study in patients with untreated low-grade follicular lymphoma. PATIENTS AND METHODS: Patients received six cycles of CVP followed by one cycle of tositumomab and (131)I-tositumomab (one dosimetric dose and one therapeutic dose). The treatment was evaluated for efficacy and safety. RESULTS: All 30 patients enrolled completed CVP as well as tositumomab and (131)I-tositumomab therapy. The overall response rate after completion of therapy was 100%, with 28 patients (93%) achieving a complete response (CR) and two patients achieving a partial response. Of the 17 patients with bone marrow involvement at enrollment, 15 achieved a confirmed CR. Fourteen of 15 patients with bulky disease (> or = 5 cm) had a CR after treatment completion. After a median follow-up of 8.4 years, the median response duration had not been reached (range, 3 to 111+ months). Five-year progression-free and overall survival rates were 56% and 83%, respectively. The most common grade > or = 3 hematologic adverse events were neutropenia (87%) and thrombocytopenia (37%). Nineteen patients received growth factor support, and three required blood product transfusions. No patients developed human antimurine antibodies. Two patients developed myelodysplastic syndrome/acute myeloid leukemia. CONCLUSION: These mature data demonstrate that sequential therapy with a non-anthracycline-containing regimen comprising CVP followed by one cycle of tositumomab and (131)I-tositumomab produced high response rates with adequate safety and durable remissions and that this regimen represents a highly active treatment for first-line therapy of follicular non-Hodgkin's lymphoma.
机译:目的:在一项未经治疗的低度滤泡性淋巴瘤患者的多中心II期研究中,评估了环磷酰胺,长春新碱和强的松(CVP)随后进行托西妥玛布和碘131((131)I)-托西妥玛布治疗的有效性和安全性。患者和方法:患者接受6个周期的CVP,然后接受一个周期的tositumomab和(131)I-tositumomab(一个剂量剂量和一个治疗剂量)。评价该治疗的功效和安全性。结果:所有30例患者均已完成CVP以及tositumomab和(131)I-tositumomab治疗。完成治疗后的总缓解率为100%,其中28位患者(93%)达到完全缓解(CR),两名患者达到部分缓解。在入组的17例骨髓受累患者中,有15例确诊为CR。 15名大块疾病(>或= 5 cm)患者中有14名在治疗完成后出现CR。中位随访8.4年后,未达到中位缓解时间(范围3到111+个月)。五年无进展生存率和总生存率分别为56%和83%。最常见的≥3级血液学不良事件是中性粒细胞减少症(87%)和血小板减少症(37%)。 19名患者获得了生长因子的支持,三例需要输血。没有患者产生人抗鼠抗体。两名患者发展为骨髓增生异常综合症/急性髓细胞性白血病。结论:这些成熟的数据表明,采用非蒽环类药物包括CVP的顺序治疗,随后一个周期的tositumomab和(131)I-tositumomab产生了高响应率,并具有足够的安全性和持久缓解性,并且该方案代表了高活性滤泡性非霍奇金淋巴瘤的一线治疗。

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