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使用贝沙罗单抗进行靶向放射免疫治疗可使晚期低度非霍奇金淋巴瘤患者获得持久缓解。

Targeted radio-immunotherapy with Bexxar produces durable remissions in patients with late stage low grade non-Hodgkin's lymphomas.

作者信息

Capizzi Robert L

出版信息

Trans Am Clin Climatol Assoc. 2004;115:255-72.

Abstract

Patients with low grade (LG) non-Hodgkin's lymphomas (NHLs) typically have a median survival of 8-10 years during which they sustain a series of responses and relapses to therapy. More than 95% of B-cell NHLs express the CD20 surface antigen, affording opportunities for CD20-directed therapy of NHL. Since 1990, 5 trials have tested the safety and efficacy of the murine CD20 MAb Tositumomab and Iodine I 131 Tositumomab (Bexxar therapeutic regimen) in 250 patients with relapsed, refractory, or transformed LG NHL. The I-131 irradiates MAb-bound cells and those within the path length of the isotope. Response rates were 56% (overall) and 30% (complete). With a median follow-up of 44.6 months, 30% of the patients achieved a long-term, durable response; median time to progressive disease or death was 5 years. Thus, a single treatment with Bexxar may produce durable responses and partially reverse the natural history of LG NHL.

摘要

低度(LG)非霍奇金淋巴瘤(NHL)患者的中位生存期通常为8至10年,在此期间他们会经历一系列对治疗的反应和复发。超过95%的B细胞NHL表达CD20表面抗原,这为NHL的CD20导向治疗提供了机会。自1990年以来,有5项试验在250例复发、难治或转化型LG NHL患者中测试了鼠源CD20单克隆抗体托西莫单抗和碘I 131托西莫单抗(Bexxar治疗方案)的安全性和有效性。I-131会照射与单克隆抗体结合的细胞以及在同位素路径长度范围内的细胞。总体缓解率为56%,完全缓解率为30%。中位随访44.6个月时,30%的患者获得了长期持久缓解;疾病进展或死亡的中位时间为5年。因此,单次使用Bexxar治疗可能产生持久缓解,并部分逆转LG NHL的自然病程。

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