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钇[90Y]替伊莫单抗注射液治疗日本非霍奇金淋巴瘤患者的疗效和安全性。

Efficacy and safety of yttrium-90 ibritumomab tiuxetan in Japanese patients with non-Hodgkin lymphoma.

机构信息

Division of Radiology, Koga Hospital 21, 3-3-8 Miyanojin, Kurume 839-0801, Japan.

出版信息

Jpn J Radiol. 2012 Oct;30(8):642-7. doi: 10.1007/s11604-012-0103-6. Epub 2012 Jul 6.

DOI:10.1007/s11604-012-0103-6
PMID:22767027
Abstract

PURPOSE

The aim of this study was to evaluate the efficacy and side effects of radioimmunotherapies with Zevalin(®) (RIT-Z) in Japanese patients with low-grade B-cell non-Hodgkin lymphoma (NHL).

MATERIALS AND METHODS

Sixty-two patients with NHL were enrolled. Based on histology, 49 of the patients had follicular lymphoma and 23 had other lesions. The response was assessed at 8-12 weeks after RIT-Z injection with PET/CT.

RESULTS

The overall response rate was 85 %. Thirty-seven (60 %) patients achieved complete remission, 16 (26 %) had partial remission, 4 (6 %) had stable disease, and 5 (8 %) had progressive disease. There was a significant correlation between the response to RIT-Z, frequency of chemotherapy, and history of prior treatment with fludarabine. There was no significant difference in efficacy according to lymphoma type, years since last chemotherapy, patient age, or disease stage at RIT-Z. Thrombocytopenia of grade 4 was significantly correlated with disease stage at RIT-Z and history of prior treatment with fludarabine. There was also no significant correlation between hematotoxicity and lymphoma type, frequency of chemotherapy, years since last chemotherapy, patient age, or history of bone marrow transplant. Anemia was significantly correlated with frequency of chemotherapy, history of bone marrow transplant, and history of prior treatment with fludarabine.

CONCLUSIONS

The response rate was high, and we were able to decrease the hematologic side effects by using RIT-Z earlier.

摘要

目的

本研究旨在评估利妥昔单抗(Zevalin®)放射性免疫疗法(RIT-Z)在日本低级别 B 细胞非霍奇金淋巴瘤(NHL)患者中的疗效和副作用。

材料和方法

共纳入 62 例 NHL 患者。根据组织学,49 例为滤泡性淋巴瘤,23 例为其他病变。在 RIT-Z 注射后 8-12 周,采用 PET/CT 评估反应。

结果

总缓解率为 85%。37 例(60%)患者达到完全缓解,16 例(26%)患者部分缓解,4 例(6%)患者病情稳定,5 例(8%)患者病情进展。RIT-Z 反应与化疗频率、既往氟达拉滨治疗史之间存在显著相关性。淋巴瘤类型、末次化疗后时间、患者年龄和 RIT-Z 时疾病分期对疗效无显著差异。血小板减少症 4 级与 RIT-Z 时疾病分期和既往氟达拉滨治疗史显著相关。血液学毒性与淋巴瘤类型、化疗频率、末次化疗后时间、患者年龄和骨髓移植史之间也无显著相关性。贫血与化疗频率、骨髓移植史和既往氟达拉滨治疗史显著相关。

结论

缓解率较高,我们能够通过更早地使用 RIT-Z 减少血液学副作用。

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