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补体C5抑制可逆转博来霉素诱导的血栓性微血管病。

Complement C5 inhibition reverses bleomycin-induced thrombotic microangiopathy.

作者信息

Salhi Sofiane, Ribes David, Faguer Stanislas

机构信息

Department of Nephrology and Organ Transplantation, Centre for Rare Renal Diseases, University Hospital of Toulouse, Toulouse, France.

Institut National de la Santé et de la Recherche Médicale, U1048-Institut des Maladies Métaboliques et Cardiovasculaires, French Intensive care Renal Network, Toulouse, France.

出版信息

Clin Kidney J. 2020 Jul 9;14(4):1275-1276. doi: 10.1093/ckj/sfaa101. eCollection 2021 Apr.

Abstract

Whether C5 blocking may improve the outcomes of patients developing chemotherapy-induced thrombotic microangiopathy (TMA) remains elusive. Lung fibrosis is a well-known complication of bleomycin, whereas TMAs are very rare (<20 cases described). Here, we report an exceptional case of a male patient that developed acute respiratory distress syndrome and TMA following administration of bleomycin, cisplatin and etoposide . Refractoriness to plasma exchanges prompted us to use eculizumab as salvage therapy. Eculizumab led to complete remission of the TMA before Day 2. However, the patient progressed towards refractory respiratory failure, suggesting that pathophysiological mechanisms of bleomycin-induced lung fibrosis and TMA differ.

摘要

C5阻断是否能改善化疗诱导的血栓性微血管病(TMA)患者的预后仍不明确。肺纤维化是博来霉素众所周知的并发症,而TMA非常罕见(报道的病例<20例)。在此,我们报告一例特殊病例,一名男性患者在使用博来霉素、顺铂和依托泊苷后发生急性呼吸窘迫综合征和TMA。对血浆置换治疗无效促使我们使用依库珠单抗作为挽救治疗。依库珠单抗在第2天之前使TMA完全缓解。然而,患者进展为难治性呼吸衰竭,提示博来霉素诱导的肺纤维化和TMA的病理生理机制不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f425/8023184/360b62af8b9d/sfaa101f1.jpg

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