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联合实体和液体活检在肺腺癌分子谱分析中的应用:来自一个真实病例的见解

Utility of combined solid and liquid biopsy for molecular profiling in lung adenocarcinoma: Insights from a real-world case.

作者信息

Bhosale Bharat, Bafna Gunj, Subramanyam Paridhy Vanniya, Salgia Kapil, Afreen Sadia, John Jinumary, Javle Vyomesh, Verma Kritika, Naavarasi N R, Peddagangannagari Sreekanth Reddy, Gorla Akhil, Periyasamy Giridharan, Rishi Kshitij, Goswami Hitesh, Veldore Vidya H

机构信息

Bombay Hospital, Mumbai, India.

BB Precision Oncocare Centre, Mumbai, India.

出版信息

J Liq Biopsy. 2025 Jun 7;8:100303. doi: 10.1016/j.jlb.2025.100303. eCollection 2025 Jun.

Abstract

Lung adenocarcinoma is a subtype of NSCLC that is often associated with poor prognosis. We present a case of metastatic lung adenocarcinoma in which comprehensive genomic profiling using both solid and liquid biopsies was employed to monitor disease progression and guide targeted therapy decisions. An initial liquid biopsy detected gene fusion, and the patient was started on Crizotinib. Following disease progression, further genomic profiling using both solid tissue and cfDNA revealed the presence of a previously undetected classical mutation exon 21, p. L858R. Consequently, the treatment was adjusted to include both Crizotinib and Gefitinib. A 6-month follow-up showed relapse and extensive metastasis. A repeat liquid biopsy identified a newly acquired mutation (exon 7, p.R248Q) in addition to the persistent mutation. Restarting the targeted therapy led to complete metabolic resolution of the disease. This case highlights the utility of liquid biopsy when tissue biopsy is not feasible and underscores the importance of integrating both solid and liquid genomic data to capture a more comprehensive mutational landscape, including low-frequency or emerging variants, ultimately enabling more effective, individualized treatment strategies.

摘要

肺腺癌是 NSCLC 的一种亚型,通常与预后不良相关。我们报告了一例转移性肺腺癌病例,其中使用实体和液体活检进行全面基因组分析,以监测疾病进展并指导靶向治疗决策。首次液体活检检测到基因融合,患者开始使用克唑替尼治疗。疾病进展后,使用实体组织和 cfDNA 进行进一步基因组分析,发现存在先前未检测到的经典突变(外显子 21,p.L858R)。因此,治疗方案调整为包括克唑替尼和吉非替尼。6 个月的随访显示疾病复发和广泛转移。再次进行液体活检发现除了持续存在的突变外,还出现了一个新获得的突变(外显子 7,p.R248Q)。重新开始靶向治疗导致疾病完全代谢缓解。该病例突出了在组织活检不可行时液体活检的实用性,并强调了整合实体和液体基因组数据以获取更全面的突变图谱(包括低频或新出现的变异)的重要性,最终实现更有效、个性化的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfdf/12179711/513eb97073db/gr1.jpg

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