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利用新型基因组测序对腋窝淋巴结病患者的原发性不明癌(CUP)进行特征分析。

Use of novel genomic sequencing to characterise carcinoma of unknown primary (CUP) in patient with axillary lymphadenopathy.

作者信息

Robertson Ian, Shaikh Kulsum, Gandia Edwin, Desmond Daniel

机构信息

Internal Medicine, Walter Reed National Military Medical Center, Bethesda, Maryland, USA

Internal Medicine, Walter Reed National Military Medical Center, Bethesda, Maryland, USA.

出版信息

BMJ Case Rep. 2025 Jan 4;18(1):e262574. doi: 10.1136/bcr-2024-262574.

DOI:10.1136/bcr-2024-262574
PMID:39755550
Abstract

Carcinoma of unknown primary (CUP) comprises 2-5% of cancer diagnoses worldwide, with a prevalence that has modestly declined with increased availability of advanced diagnostic tools such as next-generation sequencing (NGS). This case presentation illustrates the possibilities and gaps that remain with improving diagnostic capabilities in identifying and effectively treating CUP. This is the case of a rapidly enlarging right axillary mass without a primary tumour site and histological evaluation demonstrating a poorly differentiated neoplasm. Tumour of origin testing using a clinically validated RNA-sequencing-based machine learning classifier unexpectedly suggested greatest probability of metastatic melanoma with lesser likelihood of fibrosarcoma. Subsequent clinical behaviour and lack of response to chemoimmunotherapy conflicted with NGS results, with a multidisciplinary team ultimately agreeing on final diagnosis of aggressive soft tissue sarcoma, specifically malignant peripheral nerve sheath tumour. The patient had a complete clinical response after forequarter amputation and a sarcoma-based chemotherapy regimen. This case highlights both the potential and current shortcomings of NGS and predictive tumour of origin analytic tools in helping with characterisation and categorisation of CUP. There is a need for improvement and optimisation of these diagnostic modalities, but they offer another option to improve historically poor outcomes in CUP.

摘要

原发灶不明的癌(CUP)占全球癌症诊断病例的2%-5%,随着新一代测序(NGS)等先进诊断工具的普及,其发病率略有下降。本病例展示了在提高诊断能力以识别和有效治疗CUP方面存在的可能性和差距。这是一例右腋窝肿物迅速增大且无原发肿瘤部位的病例,组织学评估显示为低分化肿瘤。使用经过临床验证的基于RNA测序的机器学习分类器进行的原发灶检测意外地提示转移性黑色素瘤的可能性最大,纤维肉瘤的可能性较小。随后的临床行为以及对化疗免疫疗法缺乏反应与NGS结果相矛盾,多学科团队最终一致诊断为侵袭性软组织肉瘤,具体为恶性外周神经鞘瘤。患者在进行前半侧肢体截肢和基于肉瘤的化疗方案后获得了完全的临床缓解。本病例凸显了NGS和预测原发灶分析工具在帮助CUP的特征描述和分类方面的潜力和当前的不足。需要对这些诊断方法进行改进和优化,但它们为改善CUP历来较差的预后提供了另一种选择。

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