Remarkable response of metaplastic breast cancer to a novel targeted AKT inhibitor TAS-117 in a Cowden syndrome patient: a case report.

Eva Godina, Marta Fernández Carcaño, Burak Uzunparmak, Thomas Pepper, Pooja Shah, Jordi Rodon
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Abstract

PTEN hamartoma tumour syndrome (PHTS) is characterized by a germline PTEN mutation and a substantial increase in lifetime breast cancer risk to 85% with lower age at first diagnosis. Despite the availability of agents targeting PTEN-regulated PI3K/AKT/mTOR pathway, there are currently no approved treatments for PHTS patients with cancer. This is the first report of a patient with triple-negative metaplastic breast cancer and PHTS in the literature. We present an exceptional response of this aggressive stage IV tumour in a 34-year-old woman with PHTS to treatment with the novel AKT1-3 inhibitor, TAS-117. Despite previous rapid progression and resistance to multi-agent chemotherapy and radiotherapy, disease stabilisation was ongoing at 3.8 years. Cell-free DNA analysis of blood samples at baseline and during treatment with TAS-117 revealed a complete marker response to treatment. Therapy has been well tolerated, and the patient continues the therapy without severe adverse events, dose reduction, or treatment interruptions. These findings support further investigation of targeted interventions for malignancies developing in the context of PHTS.

一种新型靶向AKT抑制剂TAS-117对一名考登综合征患者的化生性乳腺癌的显著反应
PTEN错构瘤肿瘤综合征(PHTS)的特征是生殖系PTEN突变,并且首次诊断年龄较低,终生乳腺癌风险大幅增加至85%。尽管有靶向pten调控的PI3K/AKT/mTOR通路的药物可用,但目前尚无批准用于PHTS合并癌症患者的治疗方法。这是文献中首次报道三阴性化生乳腺癌合并PHTS的病例。我们报告了一名34岁PHTS女性患者对新型AKT1-3抑制剂TAS-117治疗的侵袭性IV期肿瘤的特殊反应。尽管先前的快速进展和对多药化疗和放疗的耐药,但疾病稳定持续3.8年。基线和TAS-117治疗期间血液样本的无细胞DNA分析显示对治疗有完全的标记反应。治疗耐受性良好,患者继续治疗,无严重不良事件、剂量减少或治疗中断。这些发现支持进一步研究PHTS背景下恶性肿瘤的靶向干预措施。
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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