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病例报告:一名患有晚期腹股沟乳腺外佩吉特病的患者接受含曲妥珠单抗的序贯治疗后获得长期临床获益。

Case Report: Prolonged clinical benefit with sequential trastuzumab-containing treatments in a patient with advanced extramammary Paget disease of the groin.

作者信息

Zattarin Emma, Nichetti Federico, Ligorio Francesca, Mazzeo Laura, Lobefaro Riccardo, Fucà Giovanni, Peverelli Giorgia, Vingiani Andrea, Bianchi Giulia V, Capri Giuseppe, de Braud Filippo, Vernieri Claudio

机构信息

Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Istituto Fondazione di Oncologia Molecolare Ente del Terzo Settore, The AIRC Institute of Molecular Oncology, Milan, Italy.

出版信息

Front Oncol. 2022 Aug 18;12:925551. doi: 10.3389/fonc.2022.925551. eCollection 2022.

Abstract

Extramammary Paget disease (EMPD) is a rare form of cutaneous, intraepithelial adenocarcinoma, which typically presents itself as an erythematous plaque originating from apocrine-gland rich regions, such as the vulva, the perianal region, the scrotum, the penis, or the axilla. EMPD patients typically have a good prognosis, with expected 5-year survival of 60%-92%, but it is estimated that about one-third of EMPD patients will develop lymph node or distant metastases. Treatment approaches for EMPD include locoregional therapies such as broad surgical resection, radiotherapy, or topical imiquimod, when the disease is localized, and chemotherapy and biological agents for advanced EMPD. We report the case of a 58-year-old man diagnosed with locally advanced, symptomatic HER2-overexpressing, AR-positive EMPD, who achieved long-term tumor control with a sequence of several trastuzumab-based treatments (more than 30 months with second-line carboplatin plus paclitaxel plus trastuzumab followed by trastuzumab maintenance; 9 months for third-line vinorelbine plus trastuzumab). Even if it is reported that AR expression occurs concomitantly with HER2 overexpression in more than half of the cases of EMPD, to the best of our knowledge, this is the first case report describing androgen receptor blockade therapy in combination with an anti-HER2 agent. Our patient did not benefit from androgen receptor blockade in combination with trastuzumab, thus suggesting that AR expression may simply reflect an intrinsic characteristic of the EMPD cell of origin, rather than tumor dependence upon AR signaling. Given the reported sensibility to anti-HER2 therapy, also new antibody drug conjugates targeting HER2 are worth exploring in the management of advanced EMPD.

摘要

乳房外佩吉特病(EMPD)是一种罕见的皮肤上皮内腺癌,通常表现为起源于富含顶泌汗腺区域的红斑性斑块,如外阴、肛周区域、阴囊、阴茎或腋窝。EMPD患者通常预后良好,预计5年生存率为60%-92%,但据估计约三分之一的EMPD患者会发生淋巴结或远处转移。EMPD的治疗方法包括局部治疗,如在疾病局限时进行广泛手术切除、放疗或外用咪喹莫特,以及晚期EMPD的化疗和生物制剂。我们报告了一例58岁男性患者,诊断为局部晚期、有症状的HER2过表达、AR阳性的EMPD,该患者通过一系列基于曲妥珠单抗的治疗实现了长期肿瘤控制(二线使用卡铂加紫杉醇加曲妥珠单抗治疗超过30个月,随后进行曲妥珠单抗维持治疗;三线使用长春瑞滨加曲妥珠单抗治疗9个月)。即使有报道称在超过一半的EMPD病例中AR表达与HER2过表达同时出现,但据我们所知,这是第一例描述雄激素受体阻断疗法联合抗HER2药物的病例报告。我们的患者未从雄激素受体阻断联合曲妥珠单抗治疗中获益,因此提示AR表达可能仅仅反映了EMPD起源细胞的内在特征,而非肿瘤对AR信号的依赖。鉴于已报道的对抗HER2治疗的敏感性,新型靶向HERX的抗体药物偶联物在晚期EMPD的治疗中也值得探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e1c/9433574/97edfc6ca616/fonc-12-925551-g001.jpg

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