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病例报告:一名乳腺癌患者在接受MK-4830和帕博利珠单抗免疫治疗期间出现苔藓样皮疹。

Case report: Lichenoid eruption under immunotherapy with MK-4830 and pembrolizumab in a breast cancer patient.

作者信息

Kachlik Zofia, Błażewicz Izabela, Ciarka Aleksandra, Nowicki Roman J

机构信息

Department of Dermatology, Venereology and Allergology, Faculty of Medicine, Medical University of Gdansk, Gdansk, Poland.

Department of Pathomorphology, Medical University of Gdansk, Gdansk, Poland.

出版信息

Front Pharmacol. 2024 Aug 13;15:1445685. doi: 10.3389/fphar.2024.1445685. eCollection 2024.

Abstract

BACKGROUND

Immune checkpoint inhibitors (ICIs) have revolutionized cancer treatment, yet they can induce immune-related adverse events (irAEs), including cutaneous toxicities such as lichenoid eruptions. Pembrolizumab, a PD-1 inhibitor, is known for its association with lichen-planus-like reactions, while the side effect profile of combining immunotherapy with MK-4830, a novel fully human IgG4 monoclonal antibody that targets ILT-4, remains limited.

CASE REPORT

We present a case of a 47-year-old female with metastatic breast cancer who developed a grade 2 Common Terminology Criteria for Adverse Events (CTCAE) lichenoid reaction after 9 months of MK-4830 and pembrolizumab use. Confluent, erythematous papules with Wickham's striae appeared predominantly on the extremities. Initial therapy with high-potency topical corticosteroids proved insufficient, however prednisone 40 mg daily resulted in satisfactory remission of lichen-planus-like reaction, permitting continued immunotherapy without dosage adjustment.

CONCLUSION

This case highlights the novel occurrence of lichenoid eruption induced by MK-4830 and pembrolizumab in breast cancer treatment. The patient was successfully treated with oral prednisone, which controlled the skin symptoms without interrupting ICI therapy. We emphasize that early diagnosis and treatment of low-grade lichenoid eruption can prevent the cessation of ICIs, thereby combining the benefits of managing irAEs and avoiding cancer progression, leading to a better long-term prognosis.

摘要

背景

免疫检查点抑制剂(ICIs)彻底改变了癌症治疗方式,但它们可诱发免疫相关不良事件(irAEs),包括苔藓样疹等皮肤毒性反应。帕博利珠单抗是一种PD-1抑制剂,因其与扁平苔藓样反应有关而闻名,而将免疫疗法与靶向ILT-4的新型全人IgG4单克隆抗体MK-4830联合使用的副作用情况仍较为有限。

病例报告

我们报告一例47岁转移性乳腺癌女性患者,在使用MK-4830和帕博利珠单抗9个月后出现了2级不良事件通用术语标准(CTCAE)苔藓样反应。融合性红斑丘疹伴威克姆纹主要出现在四肢。最初使用强效外用糖皮质激素治疗效果不佳,但每日40mg泼尼松使扁平苔藓样反应得到了满意缓解,从而可以在不调整剂量的情况下继续进行免疫治疗。

结论

该病例突出了MK-4830和帕博利珠单抗在乳腺癌治疗中诱发苔藓样疹的新情况。患者通过口服泼尼松成功治愈,该药物控制了皮肤症状且未中断ICI治疗。我们强调,对低度苔藓样疹进行早期诊断和治疗可防止停止使用ICIs,从而兼顾管理irAEs的益处并避免癌症进展,带来更好的长期预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ccf/11347415/9bcccf876450/fphar-15-1445685-g001.jpg

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