Oligometastatic Squamous Cell Transformation From Metastatic Prostate Adenocarcinoma Treated With Systemic and Focal Therapy: A Case Report.

Q3 Medicine
Journal of Immunotherapy and Precision Oncology Pub Date : 2022-06-15 eCollection Date: 2022-08-01 DOI:10.36401/JIPO-22-4
Karen Autio, Sean McBride
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引用次数: 0

Abstract

Transformation to squamous cell carcinoma (SCC) after initial treatment of a primary prostate adenocarcinoma is rare and typically results in rapid treatment-refractory disease progression and death. Here, we present a case of a 70-year-old man who was initially treated with prostatectomy and radiotherapy, and later developed bone metastases. After commencing systemic therapy with androgen deprivation therapy (ADT) and apalutamide, his prostate-specific antigen (PSA) declined to undetectable levels, yet short-interval imaging demonstrated oligo-progression at T4, with biopsy specimen demonstrating pure SCC. Molecular profiling of both the primary prostate tumor and T4 demonstrated alterations in TMPRSS2-ERG, TP53, and FOXA1 confirming site of origin, with loss of RNF43 in the squamous metastasis. He was treated with stereotactic body radiation therapy to the SCC metastasis and continued on ADT and apalutamide with stable disease for a year post-radiation. This case highlights the importance of imaging to detect non-PSA-producing metastatic disease, the utility of radiation therapy in oligo-progression, and use of molecular profiling to provide insights into the pathogenesis of histologic transformation.

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转移性前列腺癌的少转移性鳞状细胞转化经全身和局灶治疗:1例报告。
原发性前列腺癌最初治疗后转化为鳞状细胞癌(SCC)是罕见的,通常导致快速治疗难治性疾病进展和死亡。在此,我们报告一位70岁的男性患者,他最初接受前列腺切除术和放射治疗,后来发生骨转移。在开始用雄激素剥夺疗法(ADT)和阿帕鲁胺进行全身治疗后,他的前列腺特异性抗原(PSA)下降到无法检测到的水平,但短间隔成像显示在T4时低水平进展,活检标本显示纯粹的SCC。原发性前列腺肿瘤和T4的分子图谱显示TMPRSS2-ERG、TP53和FOXA1的改变证实了起源位点,而RNF43在鳞状转移中缺失。他接受立体定向放射治疗,以治疗SCC转移,并继续使用ADT和阿帕鲁胺,放射后病情稳定一年。该病例强调了影像学检测非psa产生转移性疾病的重要性,放射治疗在寡进展中的应用,以及使用分子谱分析来深入了解组织学转化的发病机制。
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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来源期刊
CiteScore
2.40
自引率
0.00%
发文量
17
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