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贝波司汀和苯海拉明对利妥昔单抗诱导的输注反应的比较抑制作用。

Comparative inhibitory effects of bepotastine and diphenhydramine on rituximab-induced infusion reactions.

作者信息

Hori Tomoki, Yamamoto Kazuhiro, Nakagawa Tomoaki, Nakagawa Rinako, Okayama Masami, Sudou Tamika, Hamasaki Moe, Yasuda Mai, Kobayashi Shinya, Nakamura Fumihiko, Yagi Hideo, Kitahiro Yumi, Ikushima Shigeki, Yano Ikuko

机构信息

Department of Pharmacy, Nara Prefecture General Medical Center, 2-897-5 Shichijo-Nishimachi, Nara, 630-8581, Japan.

Department of Pharmacy, Kobe University Hospital, 7-5-2 Kusunoki-Cho, Chuo-Ku, Kobe, 650-0017, Japan.

出版信息

Int J Hematol. 2025 Sep;122(3):413-420. doi: 10.1007/s12185-025-03990-6. Epub 2025 Apr 29.

Abstract

PURPOSE

Infusion-related reaction (IRR) is a common adverse event induced by rituximab. Although first-generation histamine 1 receptor antagonists (H1RAs) are commonly used to prevent IRR, evidence on IRR suppression by the second-generation H1RA bepotastine is scarce. In this study, we assessed the inhibitory effects of bepotastine on rituximab-induced IRR and compared them with those of the first-generation H1RA diphenhydramine.

METHODS

We retrospectively evaluated IRR incidence in patients with B-cell non-Hodgkin lymphoma who received their first dose of rituximab.

RESULTS

The incidence of any grade IRR was 9.8% in the bepotastine group (n = 92), which was significantly lower than the 30.2% rate in the diphenhydramine group (n = 96; p < 0.001). The incidence of grade 2 or higher IRR was similar between the two groups (6.5% vs. 12.5%; p = 0.16). Multivariable logistic regression analysis revealed that the risk of any grade IRR incidence was higher in patients with B symptoms and bulky disease. Premedication with bepotastine was an independent factor in reducing the risk of any grade IRR incidence (odds ratio = 0.19, 95% confidence interval: 0.08-0.47).

CONCLUSION

Bepotastine may be more effective than diphenhydramine in reducing the incidence of rituximab-induced IRR, particularly low-grade reactions.

摘要

目的

输液相关反应(IRR)是利妥昔单抗诱导的常见不良事件。虽然第一代组胺1受体拮抗剂(H1RAs)常用于预防IRR,但关于第二代H1RA倍他司汀抑制IRR的证据却很少。在本研究中,我们评估了倍他司汀对利妥昔单抗诱导的IRR的抑制作用,并将其与第一代H1RA苯海拉明的抑制作用进行比较。

方法

我们回顾性评估了接受首剂利妥昔单抗治疗的B细胞非霍奇金淋巴瘤患者的IRR发生率。

结果

倍他司汀组(n = 92)任何级别的IRR发生率为9.8%,显著低于苯海拉明组的30.2%(n = 96;p < 0.001)。两组2级或更高级别IRR的发生率相似(6.5%对12.5%;p = 0.16)。多变量逻辑回归分析显示,有B症状和肿块性疾病的患者发生任何级别的IRR的风险更高。倍他司汀预处理是降低任何级别的IRR发生风险的独立因素(比值比 = 0.19,95%置信区间:0.08 - 0.47)。

结论

倍他司汀在降低利妥昔单抗诱导的IRR发生率方面可能比苯海拉明更有效,尤其是低级别的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f399/12380942/2c0291d566f7/12185_2025_3990_Fig1_HTML.jpg

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