Case report: Liquid biopsy, the sooner the better?

The detection of circulating tumor DNA (ctDNA) by liquid biopsy is taking an increasing role in thoracic oncology management due to its predictive and prognostic value. For non-small cell lung cancer, it allows the detection of molecular mutations that can be targeted with tyrosine kinase inhibitors...

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Main Authors: Quentin Dominique Thomas, Julien Colard-Thomas, Delphine Delansay, Fanny Leenhardt, Jerome Solassol, Julie A. Vendrell, Xavier Quantin
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-12-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2022.1089108/full
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author Quentin Dominique Thomas
Quentin Dominique Thomas
Julien Colard-Thomas
Delphine Delansay
Fanny Leenhardt
Fanny Leenhardt
Jerome Solassol
Julie A. Vendrell
Xavier Quantin
Xavier Quantin
author_facet Quentin Dominique Thomas
Quentin Dominique Thomas
Julien Colard-Thomas
Delphine Delansay
Fanny Leenhardt
Fanny Leenhardt
Jerome Solassol
Julie A. Vendrell
Xavier Quantin
Xavier Quantin
author_sort Quentin Dominique Thomas
collection DOAJ
description The detection of circulating tumor DNA (ctDNA) by liquid biopsy is taking an increasing role in thoracic oncology management due to its predictive and prognostic value. For non-small cell lung cancer, it allows the detection of molecular mutations that can be targeted with tyrosine kinase inhibitors (TKIs). We report the case of a patient with life-threatening hepatocellular failure and thrombotic microangiopathy at the diagnosis. A salvage chemotherapy was attempted, resulting in a major worsening of her general condition and the decision to stop all anti-cancer treatment. The liquid biopsy performed at the time of immunohistochemical non-small cell lung cancer diagnosis revealed within 7 days the presence of an epidermal growth factor receptor (EGFR)DEL19 activating mutation with 736,400 DNA copies/ml of plasma. It was finally decided to attempt a treatment with osimertinib (third generation anti-EGFR TKI) despite the fact that the patient was in a pre-mortem situation. Osimertinib led to a significant and prompt improvement of her performance status after only one week of treatment. The tumor tissue genotyping performed by next-generation sequencing (NGS) was available 10 days after starting TKI treatment. It revealed in addition to the EGFRDEL19 mutation, a JAK3 and EGFR amplification, highlighting the complex interactions between EGFR and the JAK/STAT signaling pathways. The first CT-scan performed after 2 months under osimertinib showed a tumor morphologic partial response. The biological assay showed a major decrease in the EGFRDEL19 mutation ctDNA levels (40.0 copies/ml). The liquid biopsy allowed an early implementation of a targeted therapy without which the patient would probably be dead. Testing for ctDNA should be discussed routinely at diagnosis in addition to tumor tissue genotyping for patient with metastatic non-small cell lung cancer that raise the clinical profile of oncogenic addiction.
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spelling doaj.art-c4256822ac1d4b32936effa6be87ef772022-12-22T04:41:27ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2022-12-011210.3389/fonc.2022.10891081089108Case report: Liquid biopsy, the sooner the better?Quentin Dominique Thomas0Quentin Dominique Thomas1Julien Colard-Thomas2Delphine Delansay3Fanny Leenhardt4Fanny Leenhardt5Jerome Solassol6Julie A. Vendrell7Xavier Quantin8Xavier Quantin9Department of Medical Oncology, Montpellier Cancer Institute (ICM), Montpellier, FranceOncogenic Pathways in Lung Cancer, Montpellier Cancer Research Institute (IRCM), University of Montpellier (UM), Montpellier, FranceDepartment of Medical Oncology, Montpellier Cancer Institute (ICM), Montpellier, FranceDepartment of Medical Oncology, Montpellier Cancer Institute (ICM), Montpellier, FranceOncogenic Pathways in Lung Cancer, Montpellier Cancer Research Institute (IRCM), University of Montpellier (UM), Montpellier, FrancePharmacy department, Montpellier Cancer institute (ICM), Montpellier, FranceDepartment of Pathology, Montpellier University Hospital (CHU) Montpellier, Arnaud de Villeneuve Hospital, Montpellier, FranceDepartment of Pathology, Montpellier University Hospital (CHU) Montpellier, Arnaud de Villeneuve Hospital, Montpellier, FranceDepartment of Medical Oncology, Montpellier Cancer Institute (ICM), Montpellier, FranceOncogenic Pathways in Lung Cancer, Montpellier Cancer Research Institute (IRCM), University of Montpellier (UM), Montpellier, FranceThe detection of circulating tumor DNA (ctDNA) by liquid biopsy is taking an increasing role in thoracic oncology management due to its predictive and prognostic value. For non-small cell lung cancer, it allows the detection of molecular mutations that can be targeted with tyrosine kinase inhibitors (TKIs). We report the case of a patient with life-threatening hepatocellular failure and thrombotic microangiopathy at the diagnosis. A salvage chemotherapy was attempted, resulting in a major worsening of her general condition and the decision to stop all anti-cancer treatment. The liquid biopsy performed at the time of immunohistochemical non-small cell lung cancer diagnosis revealed within 7 days the presence of an epidermal growth factor receptor (EGFR)DEL19 activating mutation with 736,400 DNA copies/ml of plasma. It was finally decided to attempt a treatment with osimertinib (third generation anti-EGFR TKI) despite the fact that the patient was in a pre-mortem situation. Osimertinib led to a significant and prompt improvement of her performance status after only one week of treatment. The tumor tissue genotyping performed by next-generation sequencing (NGS) was available 10 days after starting TKI treatment. It revealed in addition to the EGFRDEL19 mutation, a JAK3 and EGFR amplification, highlighting the complex interactions between EGFR and the JAK/STAT signaling pathways. The first CT-scan performed after 2 months under osimertinib showed a tumor morphologic partial response. The biological assay showed a major decrease in the EGFRDEL19 mutation ctDNA levels (40.0 copies/ml). The liquid biopsy allowed an early implementation of a targeted therapy without which the patient would probably be dead. Testing for ctDNA should be discussed routinely at diagnosis in addition to tumor tissue genotyping for patient with metastatic non-small cell lung cancer that raise the clinical profile of oncogenic addiction.https://www.frontiersin.org/articles/10.3389/fonc.2022.1089108/fulllung cancerctDNA = circulating tumor DNAliquid biopsyEGFRthrombotic microangiopathy (TMA)osimertinib
spellingShingle Quentin Dominique Thomas
Quentin Dominique Thomas
Julien Colard-Thomas
Delphine Delansay
Fanny Leenhardt
Fanny Leenhardt
Jerome Solassol
Julie A. Vendrell
Xavier Quantin
Xavier Quantin
Case report: Liquid biopsy, the sooner the better?
Frontiers in Oncology
lung cancer
ctDNA = circulating tumor DNA
liquid biopsy
EGFR
thrombotic microangiopathy (TMA)
osimertinib
title Case report: Liquid biopsy, the sooner the better?
title_full Case report: Liquid biopsy, the sooner the better?
title_fullStr Case report: Liquid biopsy, the sooner the better?
title_full_unstemmed Case report: Liquid biopsy, the sooner the better?
title_short Case report: Liquid biopsy, the sooner the better?
title_sort case report liquid biopsy the sooner the better
topic lung cancer
ctDNA = circulating tumor DNA
liquid biopsy
EGFR
thrombotic microangiopathy (TMA)
osimertinib
url https://www.frontiersin.org/articles/10.3389/fonc.2022.1089108/full
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