Utility of combined solid and liquid biopsy for molecular profiling in lung adenocarcinoma: Insights from a real-world case
Bharat Bhosale, Gunj Bafna, Paridhy Vanniya Subramanyam, Kapil Salgia, Sadia Afreen, Jinumary John, Vyomesh Javle, Kritika Verma, N.R. Naavarasi, Sreekanth Reddy Peddagangannagari, Akhil Gorla, Giridharan Periyasamy, Kshitij Rishi, Hitesh Goswami, Vidya H. Veldore

TL;DR
This case study shows how combining solid and liquid biopsies can improve treatment decisions for lung cancer by tracking genetic changes over time.
Contribution
Demonstrates the added value of integrating solid and liquid biopsy data to detect emerging mutations and guide personalized therapy in lung adenocarcinoma.
Findings
Liquid biopsy identified ROS1-CCDC6 fusion, leading to Crizotinib treatment initiation.
Combined solid and liquid biopsy revealed EGFR p.L858R mutation, prompting dual therapy with Crizotinib and Gefitinib.
Liquid biopsy detected a new TP53 mutation alongside persistent EGFR mutation, enabling targeted therapy restart for disease resolution.
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 ROS1-CCDC6 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 EGFR 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 TP53 mutation (exon 7, p.R248Q) in addition to the persistent EGFR mutation. Restarting the targeted therapy led to…
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Taxonomy
TopicsMedical Imaging and Pathology Studies · Lung Cancer Treatments and Mutations · Cancer Genomics and Diagnostics
