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

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

多西他赛治疗失败后使用抗程序性细胞死亡蛋白 1 疗法治疗乳腺外 Paget 病。
乳腺外帕吉特氏病(EMPD)是一种罕见的皮肤癌,目前还没有针对晚期疾病的标准治疗方法。虽然以多西他赛为基础的化疗很常见,但没有标准治疗方法。Pembrolizumab获准用于具有高肿瘤突变负荷(TMB)和/或高微卫星不稳定性的实体瘤,nivolumab于2024年2月在日本获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)治疗EMPD的疗效,目前还缺乏真实世界的数据。我们介绍了三例在多西他赛治疗后接受抗 PD-1 治疗的 EMPD 患者的病例详情,其 TMB 值分别为 17.8、14.3 和 5.0 mut/Mb,并回顾了类似报道的病例。即使在TMB值较高的病例中,抗PD-1治疗的反应也并不充分。大多数病例涉及二线治疗或后期治疗,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疗效。
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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