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131I-托西莫单抗治疗复发或难治性惰性非霍奇金淋巴瘤后的长期完全缓解。

Long-term complete responses after 131I-tositumomab therapy for relapsed or refractory indolent non-Hodgkin's lymphoma.

作者信息

Buchegger F, Antonescu C, Delaloye A Bischof, Helg C, Kovacsovics T, Kosinski M, Mach J-P, Ketterer N

机构信息

Service of Nuclear Medicine, University Hospital of Lausanne, Switzerland.

出版信息

Br J Cancer. 2006 Jun 19;94(12):1770-6. doi: 10.1038/sj.bjc.6603166. Epub 2006 May 9.

Abstract

We present the long-term results of 18 chemotherapy relapsed indolent (N = 12) or transformed (N = 6) NHL patients of a phase II anti-CD20 (131)I-tositumomab (Bexxar) therapy study. The biphasic therapy included two injections of 450 mg unlabelled antibody combined with (131)I-tositumomab once as dosimetric and once as therapeutic activity delivering 75 or 65 cGy whole-body radiation dose to patients with normal or reduced platelet counts, respectively. Two patients were not treated due to disease progression during dosimetry. The overall response rate was 81% in the 16 patients treated, including 50% CR/CRu and 31% PR. Median progression free survival of the 16 patients was 22.5 months. Median overall survival has not been reached after a median observation of 48 months. Median PFS of complete responders (CR/CRu) has not been reached and will be greater than 51 months. Short-term side effects were mainly haematological and transient. Among the relevant long-term side effects, one patient previously treated with CHOP chemotherapy died from secondary myelodysplasia. Four patients developed HAMA. In conclusion, (131)I-tositumomab RIT demonstrated durable responses especially in those patients who achieved a complete response. Six of eight CR/CRu are ongoing after 46-70 months.

摘要

我们展示了一项II期抗CD20(131)I - 托西莫单抗(Bexxar)治疗研究中18例化疗复发的惰性(N = 12)或转化型(N = 6)非霍奇金淋巴瘤(NHL)患者的长期结果。双相疗法包括两次注射450 mg未标记抗体,与(131)I - 托西莫单抗联合使用,一次用于剂量测定,一次用于治疗活性,分别向血小板计数正常或降低的患者提供75或65 cGy的全身辐射剂量。两名患者因剂量测定期间疾病进展未接受治疗。在接受治疗的16例患者中,总缓解率为81%,包括50%的完全缓解/未确认完全缓解(CR/CRu)和31%的部分缓解(PR)。16例患者的无进展生存期中位数为22.5个月。经过48个月的中位观察期后,总生存期中位数尚未达到。完全缓解者(CR/CRu)的无进展生存期中位数尚未达到,且将超过51个月。短期副作用主要是血液学方面的且为短暂性。在相关的长期副作用中,一名先前接受过CHOP化疗的患者死于继发性骨髓发育异常。四名患者出现人抗鼠抗体(HAMA)。总之,(131)I - 托西莫单抗放射性免疫治疗显示出持久的反应,尤其是在那些达到完全缓解的患者中。8例CR/CRu患者中有6例在46 - 70个月后仍处于缓解状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e98/2361356/2a9190a1ce5c/94-6603166f1.jpg

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