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程序性细胞死亡蛋白-1 抑制剂治疗实体器官移植受者晚期皮肤鳞状细胞癌的系统评价。

Systematic review of programmed cell death-1 inhibitor therapy for advanced-stage cutaneous squamous cell carcinoma in solid-organ transplant recipients.

机构信息

Baylor College of Medicine, School of Medicine, Houston, TX, USA.

Department of Dermatology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.

出版信息

J Dermatolog Treat. 2022 Dec;33(8):3119-3126. doi: 10.1080/09546634.2022.2118516. Epub 2022 Sep 5.

Abstract

BACKGROUND

Programmed cell death-1 (PD-1) inhibitors represent an effective treatment option for advanced cutaneous squamous cell carcinoma (cSCC). However, solid organ transplant (SOT) recipients with cSCC have traditionally been excluded from clinical trials.

OBJECTIVE

To assess the safety and efficacy of PD-1 inhibitors for stage III-IV cSCC in SOT recipients.

MATERIALS & METHODS: A systematic review was performed using the PubMed, EMBASE, and Scopus databases.

RESULTS

We identified 21 articles describing 33 SOT recipients (26 kidney, four liver, two lung, and one heart) with stage III-IV cSCC treated with PD-1 inhibitors. Eleven patients (33.3%) experienced allograft rejection. Of the 25 cases with iRECIST scores, twelve patients (48.0%) had a complete response (CR), eight (32.0%) showed a partial response (PR), three (12.0%) progressive disease, and two (8.0%) stable disease (SD). Including patients without available iRECIST scores, 21 patients (63.6%) showed tumor response. Eleven patients died, with six (54.5%) due to tumor progression and one (9.1%) due to allograft rejection after foregoing dialysis.

CONCLUSION

PD-1 inhibitors demonstrate efficacy for advanced cSCC and confer a risk of allograft rejection in SOT recipients, requiring careful assessment of risks and benefits. If anti-PD-1 therapy is pursued, use of mTOR inhibitors, prophylactic steroids, and donor-derived cell-free DNA monitoring may mitigate the risk of rejection.

摘要

背景

程序性细胞死亡受体-1(PD-1)抑制剂是治疗晚期皮肤鳞状细胞癌(cSCC)的有效治疗选择。然而,患有 cSCC 的实体器官移植(SOT)受者传统上被排除在临床试验之外。

目的

评估 PD-1 抑制剂在 SOT 受者中治疗 III-IV 期 cSCC 的安全性和有效性。

材料与方法

使用 PubMed、EMBASE 和 Scopus 数据库进行系统评价。

结果

我们确定了 21 篇描述了 33 例接受 PD-1 抑制剂治疗的 III-IV 期 cSCC 的 SOT 受者(26 例肾脏、4 例肝脏、2 例肺和 1 例心脏)的文章。11 例患者(33.3%)发生同种异体移植物排斥反应。在 25 例具有 iRECIST 评分的病例中,12 例患者(48.0%)完全缓解(CR),8 例(32.0%)部分缓解(PR),3 例(12.0%)疾病进展,2 例(8.0%)稳定疾病(SD)。包括没有可用 iRECIST 评分的患者,21 例(63.6%)患者有肿瘤反应。11 例患者死亡,其中 6 例(54.5%)因肿瘤进展,1 例(9.1%)因透析后发生同种异体移植物排斥而死亡。

结论

PD-1 抑制剂对晚期 cSCC 有效,并在 SOT 受者中引起同种异体移植物排斥的风险,需要仔细评估风险和获益。如果追求抗 PD-1 治疗,可以使用 mTOR 抑制剂、预防性类固醇和供体无细胞游离 DNA 监测来降低排斥反应的风险。

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