Pembrolizumab associated immune thrombocytopenia.

IF 1.9 4区 医学 Q3 INFECTIOUS DISEASES
Perihan Perkin, Serhat Sekmek, Dogan Bayram, Fahriye Tugba Kos
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引用次数: 0

Abstract

Immune checkpoint inhibitors (ICIs) have revolutionized cancer treatment but are associated with immune-related adverse events (irAEs). Pembrolizumab, an anti-PD-1 antibody, is widely used in non-small cell lung cancer (NSCLC), yet immune thrombocytopenia remains a rare but potentially fatal complication. We report a case of a 55-year-old male with metastatic NSCLC who developed pembrolizumab-associated immune thrombocytopenia. The patient initially responded well to combination therapy with pembrolizumab, carboplatin, and pemetrexed, achieving a metabolic complete response. However, after several cycles, he experienced recurrent grade 3 thrombocytopenia. Immune thrombocytopenia was suspected and managed with corticosteroids, leading to platelet recovery. Upon pembrolizumab rechallenge, thrombocytopenia recurred, necessitating permanent discontinuation of pembrolizumab while continuing pemetrexed maintenance. This case underscores the need for early recognition and prompt management of ICI-induced thrombocytopenia to ensure patient safety while optimizing oncologic outcomes.

派姆单抗相关的免疫性血小板减少症。
免疫检查点抑制剂(ICIs)已经彻底改变了癌症治疗,但与免疫相关不良事件(irAEs)相关。Pembrolizumab是一种抗pd -1抗体,广泛用于非小细胞肺癌(NSCLC),但免疫性血小板减少症仍然是一种罕见但潜在致命的并发症。我们报告一例55岁男性转移性非小细胞肺癌,并发派姆单抗相关免疫性血小板减少症。患者最初对派姆单抗、卡铂和培美曲塞联合治疗反应良好,实现了代谢完全缓解。然而,几个周期后,他经历了复发的3级血小板减少症。怀疑免疫性血小板减少症并使用皮质类固醇治疗,导致血小板恢复。在派姆单抗再次挑战后,血小板减少症复发,需要永久停药派姆单抗,同时继续培美曲塞维持。该病例强调了早期识别和及时管理ici诱导的血小板减少症的必要性,以确保患者安全,同时优化肿瘤预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Chemotherapy
Journal of Chemotherapy 医学-药学
CiteScore
3.70
自引率
0.00%
发文量
144
审稿时长
6-12 weeks
期刊介绍: The Journal of Chemotherapy is an international multidisciplinary journal committed to the rapid publication of high quality, peer-reviewed, original research on all aspects of antimicrobial and antitumor chemotherapy. The Journal publishes original experimental and clinical research articles, state-of-the-art reviews, brief communications and letters on all aspects of chemotherapy, providing coverage of the pathogenesis, diagnosis, treatment, and control of infection, as well as the use of anticancer and immunomodulating drugs. Specific areas of focus include, but are not limited to: · Antibacterial, antiviral, antifungal, antiparasitic, and antiprotozoal agents; · Anticancer classical and targeted chemotherapeutic agents, biological agents, hormonal drugs, immunomodulatory drugs, cell therapy and gene therapy; · Pharmacokinetic and pharmacodynamic properties of antimicrobial and anticancer agents; · The efficacy, safety and toxicology profiles of antimicrobial and anticancer drugs; · Drug interactions in single or combined applications; · Drug resistance to antimicrobial and anticancer drugs; · Research and development of novel antimicrobial and anticancer drugs, including preclinical, translational and clinical research; · Biomarkers of sensitivity and/or resistance for antimicrobial and anticancer drugs; · Pharmacogenetics and pharmacogenomics; · Precision medicine in infectious disease therapy and in cancer therapy; · Pharmacoeconomics of antimicrobial and anticancer therapies and the implications to patients, health services, and the pharmaceutical industry.
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