Stevens-Johnson syndrome and toxic epidermal necrolysis-like eruptions in patients treated with immune checkpoint inhibitors: a systematic review

IF 3.5 4区 医学 Q1 DERMATOLOGY International Journal of Dermatology Pub Date : 2024-09-16 DOI:10.1111/ijd.17479
Christeebella O. Akpala, Yassaman J. Erfani, Jordan Young, Vahide Saeidi, Austin Todd, Cynthia Chelf, Elizabeth J. Philips, Afsaneh Alavi
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Abstract

Background

Immune checkpoint inhibitors (ICIs) have transformed cancer treatment by targeting immune checkpoints such as PD-1, PDL-1, and CTLA-4, but concerns about severe immune-related adverse events persist. The scarcity of literature on dermatologic implications, especially severe reactions such as Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN), highlights the urgent need for investigation.

Objective

Our systematic review aims to address the gap in relevant literature by extensively examining the epidemiologic risk factors and management of SJS/TEN-like illnesses in ICI-treated patients to provide insights for risk assessment and clinical care.

Methods

We identified 158 case reports that detailed the incidence of SJS/TEN in patients being treated with ICIs, examining demographic patterns, type of malignancy, clinical characteristics, and treatments linked to onset. We assessed mortality rates, risk elements, and the effectiveness of interventions to help guide clinical care.

Results

Analysis of 158 case reports revealed that SJS/TEN in ICI users is typically seen on average at the age of 63 and is more common in males. PD1 inhibitors such as nivolumab and pembrolizumab are often associated with various mucocutaneous patterns and significant risks with ICI use, especially TEN, which is linked to high morbidity and mortality rates.

Limitations

Our study notes limitations due to the inclusion of case reports or case series, such as potential publication and reporting biases, leading to skewed findings. Additionally, because of the heterogeneous reporting standards, the retrospective nature limits phenotypic precision, control for confounding variables, and data completeness.

Conclusion

Our study provides valuable insights into the epidemiology, clinical features, management strategies, and outcomes of ICI-induced SJS/TEN, underscoring the importance of vigilant monitoring and personalized risk assessment in oncology practice. Continued research efforts are essential to optimize patient outcomes and enhance the safety profile of ICIs in cancer therapy.

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接受免疫检查点抑制剂治疗的患者出现史蒂文斯-约翰逊综合征和中毒性表皮坏死样糜烂:系统综述。
背景:免疫检查点抑制剂(ICIs)以PD-1、PDL-1和CTLA-4等免疫检查点为靶点,改变了癌症治疗方法,但与免疫相关的严重不良反应仍令人担忧。有关皮肤病影响,尤其是史蒂文斯-约翰逊综合征(Stevens-Johnson Syndrome,SJS)和中毒性表皮坏死(Toxic epidermal necrolysis,TEN)等严重不良反应的文献极少,这凸显了研究的迫切性:我们的系统综述旨在通过广泛研究 ICI 治疗患者 SJS/TEN 类疾病的流行病学风险因素和处理方法来填补相关文献的空白,从而为风险评估和临床治疗提供见解:我们确定了158份病例报告,这些报告详细描述了接受ICIs治疗的患者中SJS/TEN的发病率,研究了人口统计学模式、恶性肿瘤类型、临床特征以及与发病相关的治疗方法。我们评估了死亡率、风险因素和干预措施的有效性,以帮助指导临床治疗:对158份病例报告的分析表明,使用ICI的SJS/TEN患者通常平均年龄为63岁,男性更为常见。PD1抑制剂(如nivolumab和pembrolizumab)通常与各种粘膜形态有关,ICI使用时存在重大风险,尤其是TEN,它与高发病率和高死亡率有关:我们的研究注意到由于纳入了病例报告或系列病例而存在的局限性,如潜在的出版和报告偏差,导致研究结果偏差。此外,由于报告标准不一,回顾性研究限制了表型的精确性、混杂变量的控制以及数据的完整性:我们的研究为ICI诱发的SJS/TEN的流行病学、临床特征、管理策略和结果提供了宝贵的见解,强调了肿瘤学实践中警惕性监测和个性化风险评估的重要性。要优化患者的预后并提高 ICIs 在癌症治疗中的安全性,必须继续开展研究工作。
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来源期刊
CiteScore
4.70
自引率
2.80%
发文量
476
审稿时长
3 months
期刊介绍: Published monthly, the International Journal of Dermatology is specifically designed to provide dermatologists around the world with a regular, up-to-date source of information on all aspects of the diagnosis and management of skin diseases. Accepted articles regularly cover clinical trials; education; morphology; pharmacology and therapeutics; case reports, and reviews. Additional features include tropical medical reports, news, correspondence, proceedings and transactions, and education. The International Journal of Dermatology is guided by a distinguished, international editorial board and emphasizes a global approach to continuing medical education for physicians and other providers of health care with a specific interest in problems relating to the skin.
期刊最新文献
Enriched class II HLA inherence in patients with checkpoint inhibitor-associated bullous pemphigoid. External validation study of Re-SCORTEN in patients with Stevens-Johnson syndrome and toxic epidermal necrolysis. Issue Information No improved disease-specific survival with wide margin Mohs surgery for malignant melanoma of the skin: a retrospective cohort analysis. Blisters as a primary manifestation of systemic amyloidosis.
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