CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:(Un-)Known Chances: Emerging Hope for Cancer of Unknown Primary - Highlights from ESMO 2025 and the First International Cancer of Unknown Primary Meeting.
(Un-)Known Chances: Emerging Hope for Cancer of Unknown Primary - Highlights from ESMO 2025 and the First International Cancer of Unknown Primary Meeting.
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(i) 全基因组和转录组测序,尤其是在多学科肿瘤委员会中整合应用时,可能显著提高诊断精确度和组织起源预测,并可能进一步与 CUP 患者生存改善相关。(ii) 基于液体活检的检测为分子分层和组织起源预测提供了互补的、微创的方法,且周转时间比经典组织测序更快。(iii) 成纤维细胞活化蛋白抑制剂 PET-CT 在改善原发肿瘤和转移灶检测方面优于 FDG-PET-CT,显示出前景。(iv) 肿瘤不可知治疗策略,例如 KRAS 选择性抑制剂和 T 细胞受体工程化 T 细胞疗法,可能为 CUP 的分子驱动治疗奠定基础。
原发灶不明癌(CUP)占新诊断癌症的1-3%,在生物学上具有高度异质性,在临床上仍是一类极具挑战性的疾病。数十年来,其治疗一直依赖经验性铂类化疗,预后较差,中位总生存期通常不足1年。近年来,全面基因组分析、液体活检、功能影像学以及肿瘤不可知论药物研发方面的进展,可能改变CUP管理的诊断和治疗范式。摘要:本综述综合了ESMO 2025和首届国际原发灶不明癌会议(ICUPM)上呈现的当前及即将发布的数据,并结合近期同行评审文献。我们重点介绍新兴的诊断策略,包括全基因组和转录组测序、基于ctDNA的组织来源和癌症信号来源检测,以及应用于CUP的新型影像学方法。我们进一步讨论多学科分子肿瘤委员会的临床影响、早期检测方法以及肿瘤不可知论治疗策略,包括KRAS靶向治疗和T细胞受体工程化细胞疗法。
BACKGROUND: Cancer of unknown primary (CUP) accounts for 1-3% of newly diagnosed cancers and remains a biologically heterogeneous and clinically challenging entity. For decades, management has relied on empirical platinum-based chemotherapy, which offers a poor prognosis with a median overall survival typically below 1 year. Recent advances in comprehensive genomic profiling, liquid biopsy, functional imaging, and tumour-agnostic drug development may transform diagnostic and therapeutic paradigms for the management of CUP. SUMMARY: This review synthesises current and upcoming data presented at ESMO 2025 and the first International Cancer of Unknown Primary Meeting (ICUPM), integrated with recent peer-reviewed literature. We highlight emerging diagnostic strategies, including whole-genome and transcriptome sequencing, ctDNA-based tissue-of-origin and cancer signal origin assays, and novel imaging modalities applied to CUP. We further discuss the clinical impact of multimodal molecular tumour boards, early detection approaches, and tumour-agnostic treatment strategies, including KRAS-directed and T-cell receptor-engineered cellular therapies. KEY MESSAGES: (i) Whole-genome and transcriptome sequencing, particularly when integrated within multidisciplinary tumour boards, may substantially improve diagnostic precision and tissue-of-origin prediction and may further be associated with improved survival in CUP patients. (ii) Liquid biopsy-based assays provide complementary, minimally invasive approaches for molecular stratification and tissue-of-origin prediction, with faster turnaround times than classical tissue sequencing. (iii) Fibroblast activation protein inhibitor PET-CT shows promise in improving primary tumour and metastasis detection beyond FDG-PET-CT. (iv) Tumour-agnostic treatment strategies, e.g., KRAS-selective inhibitors and T-cell receptor-engineered T-cell therapy, may advance the groundwork for molecularly driven treatment for CUP.
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