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细胞液体活检为罕见唾液腺癌患者的疾病监测、临床前模型生成和治疗调整提供了独特的机会。

Cellular liquid biopsy provides unique chances for disease monitoring, preclinical model generation and therapy adjustment in rare salivary gland cancer patients.

作者信息

Stojanović Gužvić Nataša, Lüke Florian, Treitschke Steffi, Coluccio Andrea, Hoffmann Martin, Feliciello Giancarlo, Varadarajan Adithi Ravikumar, Lu Xin, Weidele Kathrin, Botteron Catherine, Materna-Reichelt Silvia, Keil Felix, Evert Katja, Weber Florian, Schamberger Thomas, Althammer Michael, Grosse Jirka, Hellwig Dirk, Schulz Christian, Seitz Stephan, Ugocsai Peter, Schlenska-Lange Anke, Mayr Roman, Kaiser Ulrich, Dietmaier Wolfgang, Polzer Bernhard, Warfsmann Jens, Honarnejad Kamran, Pukrop Tobias, Heudobler Daniel, Klein Christoph A, Werno Christian

机构信息

Fraunhofer Institute for Toxicology and Experimental Medicine ITEM-R, Germany.

Department of Internal Medicine III, University Hospital Regensburg, Germany.

出版信息

Mol Oncol. 2024 Oct 5. doi: 10.1002/1878-0261.13741.

DOI:10.1002/1878-0261.13741
PMID:39367702
Abstract

While cell-free liquid biopsy (cfLB) approaches provide simple and inexpensive disease monitoring, cell-based liquid biopsy (cLB) may enable additional molecular genetic assessment of systemic disease heterogeneity and preclinical model development. We investigated 71 blood samples of 62 patients with various advanced cancer types and subjected enriched circulating tumor cells (CTCs) to organoid culture conditions. CTC-derived tumoroid models were characterized by DNA/RNA sequencing and immunohistochemistry, as well as functional drug testing. Results were linked to molecular features of primary tumors, metastases, and CTCs; CTC enumeration was linked to disease progression. Of 52 samples with positive CTC counts (≥1) from eight different cancer types, only CTCs from two salivary gland cancer (SGC) patients formed tumoroid cultures (P = 0.0005). Longitudinal CTC enumeration of one SGC patient closely reflected disease progression during treatment and revealed metastatic relapse earlier than clinical imaging. Multiomics analysis and functional in vitro drug testing identified potential resistance mechanisms and drug vulnerabilities. We conclude that cLB might add a functional dimension (to the genetic approaches) in the personalized management of rare, difficult-to-treat cancers such as SGC.

摘要

虽然游离液体活检(cfLB)方法可提供简单且经济的疾病监测,但基于细胞的液体活检(cLB)可能有助于对系统性疾病异质性进行额外的分子遗传学评估以及临床前模型的开发。我们研究了62例患有各种晚期癌症类型患者的71份血样,并将富集的循环肿瘤细胞(CTC)置于类器官培养条件下。通过DNA/RNA测序、免疫组织化学以及功能药物测试对源自CTC的肿瘤样模型进行了表征。结果与原发性肿瘤、转移灶和CTC的分子特征相关联;CTC计数与疾病进展相关联。在来自八种不同癌症类型的52份CTC计数呈阳性(≥1)的样本中,只有两名唾液腺癌(SGC)患者的CTC形成了肿瘤样培养物(P = 0.0005)。一名SGC患者的纵向CTC计数密切反映了治疗期间的疾病进展,并且比临床影像学更早地发现了转移复发。多组学分析和体外功能药物测试确定了潜在的耐药机制和药物易感性。我们得出结论,cLB可能会在诸如SGC等罕见、难治性癌症的个性化管理中(为基因方法)增加一个功能维度。

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Circulating tumor cells: biology and clinical significance.循环肿瘤细胞:生物学和临床意义。
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分析尿液中游离 DNA 中的反复保护的基因组区域。
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