Liquid biopsy perspectives in pleomorphic carcinoma of the lung: case report.

IF 3.5 2区 医学 Q2 ONCOLOGY
Translational lung cancer research Pub Date : 2025-06-30 Epub Date: 2025-06-19 DOI:10.21037/tlcr-2024-1275
Tania Rossi, Michela Cortesi, Michele Zanoni, Sara Bandini, Camilla Sbrighi, Davide Angeli, Valentina Masciale, Giulia Grisendi, Matteo Costantini, Franco Stella, Paola Ulivi, Beatrice Aramini
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引用次数: 0

Abstract

Background: Liquid biopsy has recently made it possible to use minimally invasive testing to examine tumor-derived material released into peripheral blood, including circulating tumor cells (CTCs), extracellular vesicles (EVs), and circulating tumor deoxyribonucleic acid (ctDNA). Lung pleomorphic carcinoma (PC) is an extremely rare and severe form of cancer. Although resection tissues are the basis for PC diagnosis in everyday practice, tiny biopsies and cytologic specimens might potentially raise suspicions. Because PC may show varied expression of conventional carcinoma markers, it can be particularly challenging to differentiate sarcomatoid (i.e., spindle cell or giant cell) components from other tumor forms, such as sarcomatoid mesothelioma and other sarcomas. We think that defining a more specific context to better understand patient prognosis may be aided by the discovery of blood molecular markers in PC.

Cases description: We present two cases of patients underwent major lung resection at our center with a diagnosis of PC of the lung; specifically, according with 8th TNM edition, case 1 showed a final pathological stage pathological tumor-node-metastasis (pTNM): pT1cN0G3LV0R0, and case 2 showed a stage pTNM: pT3N0G3LV0R0. Patients were both discharged after surgery with no postoperative complications. Oncologists suggested a 5-year clinical and radiological follow-up, however case 1 patient is free from recurrence at the moment, while case 2 patient died for brain recurrence 10 months after surgery. Immediately after surgical resection, patient's specimens were sent to the pathology unit. The pathologist, without affecting the accuracy of histological diagnosis, selected representative tissue samples and sent them at 4 ℃ in specific media, to Bioscience Laboratory, IRCCS IRST "Dino Amadori" for tissue analysis. Additionally, blood samples collected before surgery were sent for the characterization of CTCs and EVs.

Conclusions: To better characterize the potential relationship between the presence of CTCs, EVs and high grade of malignancy and any subsequent connection to death and/or recurrence, we think that liquid biopsy, which involves the identification and characterization of tumor-derived elements, may serve as future approach and tool not only in NSCLC but also in each specific histotype as for lung PC.

多形性肺癌的液体活检透视:1例报告。
背景:液体活检最近使微创检测释放到外周血中的肿瘤来源物质成为可能,包括循环肿瘤细胞(CTCs)、细胞外囊泡(ev)和循环肿瘤脱氧核糖核酸(ctDNA)。肺多形性癌(PC)是一种极其罕见和严重的癌症。虽然在日常实践中,切除组织是诊断PC的基础,但微小的活检和细胞学标本可能会引起怀疑。由于PC可能表现出不同的常规癌标志物表达,因此将类肉瘤(即梭形细胞或巨细胞)成分与其他肿瘤形式(如类肉瘤间皮瘤和其他肉瘤)区分开来尤其具有挑战性。我们认为,通过发现PC中的血液分子标记物,可以确定更具体的情况,以更好地了解患者预后。病例描述:我们报告两例患者在我们中心接受了大肺切除术,诊断为肺PC;其中,根据第8版TNM,病例1最终病理分期为病理肿瘤-淋巴结转移(pTNM): pT1cN0G3LV0R0,病例2最终病理分期为pTNM: pT3N0G3LV0R0。两例患者均术后出院,无术后并发症。肿瘤学家建议进行5年临床及影像学随访,但病例1目前无复发,而病例2术后10个月因脑复发死亡。手术切除后,患者的标本立即送到病理部门。病理学家在不影响组织学诊断准确性的前提下,选取有代表性的组织样本,在特定培养基中,于4℃下送至IRCCS IRST“Dino Amadori”生物科学实验室进行组织分析。此外,术前采集的血液样本被送去表征ctc和ev。结论:为了更好地描述ctc、EVs的存在与高恶性肿瘤之间的潜在关系,以及与死亡和/或复发的任何后续联系,我们认为液体活检,包括肿瘤源性元素的识别和表征,可能不仅是在NSCLC中,而且在肺PC的每种特定组织型中都可以作为未来的方法和工具。
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
7.20
自引率
2.50%
发文量
137
期刊介绍: Translational Lung Cancer Research(TLCR, Transl Lung Cancer Res, Print ISSN 2218-6751; Online ISSN 2226-4477) is an international, peer-reviewed, open-access journal, which was founded in March 2012. TLCR is indexed by PubMed/PubMed Central and the Chemical Abstracts Service (CAS) Databases. It is published quarterly the first year, and published bimonthly since February 2013. It provides practical up-to-date information on prevention, early detection, diagnosis, and treatment of lung cancer. Specific areas of its interest include, but not limited to, multimodality therapy, markers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to lung cancer.
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