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病例报告:帕博利珠单抗引起肺鳞癌患者中性粒细胞减少症1例并文献复习

Case report: A rare case of neutropenia caused by pembrolizumab in squamous lung cancer and literature review.

作者信息

Tan Qiaoyun, Liu Lichao, Huang Yu, Dong Xiaorong, Chen Lingjuan

机构信息

Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Front Oncol. 2022 Nov 25;12:973421. doi: 10.3389/fonc.2022.973421. eCollection 2022.

Abstract

BACKGROUND

Immune checkpoint inhibitors, including anti-PD-1 therapies, have prolonged overall survival in patients with a variety of cancers, and immunotherapy is sometimes associated with immune-related adverse events (irAEs); however, hematological toxicity, especially neutropenia, is rare.

CASE PRESENTATION

A 78-year-old man with squamous lung cancer, with brain metastasis, was treated with pembrolizumab and albumin-bound paclitaxel as first-line treatment for one cycle and changed to pembrolizumab plus anlotinib at the second cycle. After two therapy cycles, grade 4 neutropenia developed, which mainly contributed to irAEs. The patient was started on granulocyte colony-stimulating factor (G-CSF) but did not improve; he was then treated with corticosteroids, and neutrophil counts gradually returned to normal levels. However, the patient eventually died because of neurological problems.

CONCLUSION

Grade 4 neutropenia associated with ICI, although rare, is often severe and presents with infectious complications; it needs to be diagnosed early, and clinicians should ensure prompt and proper management to such patients.

摘要

背景

免疫检查点抑制剂,包括抗程序性死亡蛋白1(PD-1)疗法,已延长了多种癌症患者的总生存期,且免疫疗法有时会伴有免疫相关不良事件(irAE);然而,血液学毒性,尤其是中性粒细胞减少症较为罕见。

病例介绍

一名78岁的鳞状肺癌伴脑转移男性患者,一线接受帕博利珠单抗和白蛋白结合型紫杉醇治疗一个周期,第二个周期改为帕博利珠单抗加安罗替尼治疗。两个治疗周期后,出现4级中性粒细胞减少症,这主要导致了免疫相关不良事件。患者开始使用粒细胞集落刺激因子(G-CSF)治疗,但病情未改善;随后接受皮质类固醇治疗,中性粒细胞计数逐渐恢复至正常水平。然而,患者最终因神经系统问题死亡。

结论

与免疫检查点抑制剂相关的4级中性粒细胞减少症虽然罕见,但通常较为严重,并伴有感染性并发症;需要早期诊断,临床医生应确保对此类患者进行及时、恰当的管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d26d/9732564/3fc44bfb10f3/fonc-12-973421-g001.jpg

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