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多西他赛治疗失败后采用抗程序性细胞死亡蛋白1疗法治疗的乳腺外佩吉特病

Extramammary Paget's disease treated with of anti-programmed cell death protein 1 therapy after docetaxel therapy failure.

作者信息

Narasaki Midori, Kato Junji, Sato Sayuri, Hida Tokimasa, Horimoto Kohei, Matsui Yoshiyuki, Shigyo Nobuaki, Uhara Hisashi

机构信息

Department of Dermatology, Sapporo Medical University School of Medicine, Sapporo, Japan.

出版信息

J Dermatol. 2025 Feb;52(2):359-362. doi: 10.1111/1346-8138.17500. Epub 2024 Oct 26.

Abstract

Extramammary Paget's disease (EMPD) is a rare skin cancer with no standard treatment for advanced-stage disease. Although docetaxel-based chemotherapy is common, no standard treatment exists. Pembrolizumab is approved for solid tumors with a high tumor mutation burden (TMB) and/or high microsatellite instability, and nivolumab was approved in Japan in February 2024 for unresectable advanced or recurrent epithelial skin malignancies. However, there is a lack of real-world data regarding the efficacy of anti-programmed cell death protein 1 (PD-1) therapy for EMPD. We present the case details of three EMPD patients treated with anti-PD-1 therapy after docetaxel treatment, with TMB values of 17.8, 14.3, and 5.0 mut/Mb, respectively, and we review similar reported cases. Even in the cases with a high TMB, the response to anti-PD-1 therapy was not sufficient. Most cases involve second-line or later treatments, so further research is needed to determine the precise effectiveness of anti-PD-1 therapy as a first-line treatment.

摘要

乳房外佩吉特病(EMPD)是一种罕见的皮肤癌,对于晚期疾病尚无标准治疗方法。尽管基于多西他赛的化疗很常见,但不存在标准治疗方案。帕博利珠单抗被批准用于治疗具有高肿瘤突变负荷(TMB)和/或高微卫星不稳定性的实体瘤,纳武利尤单抗于2024年2月在日本被批准用于不可切除的晚期或复发性上皮性皮肤恶性肿瘤。然而,关于抗程序性细胞死亡蛋白1(PD-1)疗法治疗EMPD的疗效,缺乏真实世界的数据。我们介绍了3例在多西他赛治疗后接受抗PD-1疗法的EMPD患者的病例细节,其TMB值分别为17.8、14.3和5.0个突变/Mb,并回顾了类似的报道病例。即使在TMB较高的病例中,抗PD-1疗法的反应也不充分。大多数病例涉及二线或更后续的治疗,因此需要进一步研究以确定抗PD-1疗法作为一线治疗的确切有效性。

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