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R-CHOP 样方案治疗弥漫性大 B 细胞/滤泡性淋巴瘤患者的药物性肺炎风险与粒细胞集落刺激因子的使用有关。

Drug-induced pneumonitis risk in diffuse large B-cell/follicular lymphoma patients treated with R-CHOP-like regimen is associated with the use of granulocyte colony-stimulating growth factors.

机构信息

Faculty of Health Medicine, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland.

Department of Pediatrics, Kuopio University Hospital, Kuopio, Finland.

出版信息

Cancer Med. 2024 Jan;13(1):e6898. doi: 10.1002/cam4.6898. Epub 2024 Jan 1.

Abstract

BACKGROUND

Rituximab-based combinations are the standard of care in diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL). Despite being on market for over 20 years, some of the adverse effects associated with the use of rituximab are not well known. Drug-induced interstitial pneumonitis (DIP) is a potentially fatal complication of the treatment. Granulocyte colony-stimulating factors (G-CSF) are supportive agents commonly used to prevent neutropenic infections. G-CSF are reported to have pulmonary toxicity, but the risk of DIP is greater when used in combination with other potentially pulmotoxic agents.

METHODS

In this retrospective study, we reported the G-CSF use and risk of DIP in 234 DLBCL patients and 87 FL patients receiving R-CHOP-type immunochemotherapy.

RESULTS

In 72% of patients, the treatment included a G-CSF support. The overall incidence of treatment-induced pneumonitis was 6.9% in this patient group. All the DIP cases (n = 16) were among patients receiving G-CSF support (p = 0.03). Older age (over 60 years) and higher disease stage (Ann Arbor 3-4) also increased the risk of DIP.

CONCLUSIONS

These findings suggest that the use of G-CSF increases the risk of DIP, when used in combination with rituximab-containing regimen.

摘要

背景

基于利妥昔单抗的联合治疗是弥漫性大 B 细胞淋巴瘤(DLBCL)和滤泡性淋巴瘤(FL)的标准治疗方法。尽管利妥昔单抗已经上市超过 20 年,但它的一些不良反应仍不为人知。药物诱导的间质性肺炎(DIP)是该药物治疗的一种潜在致命并发症。粒细胞集落刺激因子(G-CSF)是一种常用的支持性药物,用于预防中性粒细胞减少性感染。据报道,G-CSF 具有肺毒性,但与其他潜在的肺毒性药物联合使用时,DIP 的风险更大。

方法

在这项回顾性研究中,我们报告了 234 例接受 R-CHOP 型免疫化疗的 DLBCL 患者和 87 例 FL 患者中 G-CSF 的使用情况和 DIP 风险。

结果

在 72%的患者中,治疗包括 G-CSF 支持。在该患者群体中,治疗引起的肺炎的总发生率为 6.9%。所有 DIP 病例(n=16)均发生在接受 G-CSF 支持的患者中(p=0.03)。年龄较大(超过 60 岁)和较高的疾病分期(Ann Arbor 3-4)也增加了 DIP 的风险。

结论

这些发现表明,当与包含利妥昔单抗的方案联合使用时,G-CSF 的使用会增加 DIP 的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f22/10807566/206cc761850b/CAM4-13-e6898-g003.jpg

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