Plasma-first: accelerating lung cancer diagnosis and molecular profiling through liquid biopsy

Author:

Garcia-Pardo Miguel1ORCID,Czarnecka Kasia2,Law Jennifer H.1,Salvarrey Alexandra3,Fernandes Roxanne1,Fan Jason1,Corke Lucy1,Waddell Thomas K.4,Yasufuku Kazuhiro4,Donahoe Laura L.4,Pierre Andrew4,Le Lisa W.5,Ghumman Noor1,Liu Geoffrey1,Shepherd Frances A.1,Bradbury Penelope1,Sacher Adrian1,Stockley Tracy6,Pal Prodipto6,Rogalla Patrik7,Tsao Ming Sound6,Leighl Natasha B.8

Affiliation:

1. Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada

2. Division of Respirology, Toronto General Hospital, University Health Network, Toronto, ON, Canada

3. Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, CanadaDivision of Thoracic Surgery, Toronto General Hospital, University Health Network, Toronto, ON, Canada

4. Division of Thoracic Surgery, Toronto General Hospital, University Health Network, Toronto, ON, Canada

5. Department of Biostatistics, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada

6. Department of Laboratory Medicine and Pathobiology, Toronto General Hospital, University Health Network, Toronto, ON, Canada

7. Joint Department of Medical Imaging, Toronto General Hospital, University Health Network, Toronto, ON, Canada

8. Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, 7-913 700 University Avenue, Toronto, ON M5G 1Z5, Canada

Abstract

Introduction: Molecular profiling of tumor tissue is the gold standard for treatment decision-making in advanced non-small cell lung cancer (NSCLC). Results may be delayed or unavailable due to insufficient tissue, prolonged wait times for biopsy, pathology assessment and testing. We piloted the use of plasma testing in the initial diagnostic workup for patients with suspected advanced lung cancer. Methods: Patients with ⩽15 pack-year smoking history and suspected advanced lung cancer referred to the lung cancer rapid diagnostic program underwent plasma circulating-tumor DNA testing using a DNA-based mutation panel. Tissue testing was performed per standard of care, including comprehensive next-generation sequencing (NGS). The primary endpoint was time from diagnostic program referral to cancer treatment in stage IV NSCLC patients (Cohort A) compared to a contemporary cohort not enrolled in the study (Cohort B) and an historical pre-COVID cohort referred to the program between 2018 and 2019 (Cohort C). Results: From January to June 2021, 20 patients were enrolled in Cohort A; median age was 70.5 years (range 33–87), 70% were female, 55% Caucasian, 85% never smokers, and 75% were diagnosed with NSCLC. Seven had actionable alterations detected in plasma or tissue (4/7 concordant). Fusions, not tested in plasma, were identified by immunohistochemistry for three patients. Mean result turnaround time was 17.8 days for plasma NGS and 23.6 days for tissue ( p = 0.10). Mean time from referral to treatment initiation was significantly shorter in cohort A at 32.6 days (SD 13.1) versus 62.2 days (SD 31.2) in cohort B and 61.5 days (SD 29.1) in cohort C, both p < 0.0001. Conclusion: Liquid biopsy in the initial diagnostic workup of patients with suspected advanced NSCLC can lead to faster molecular results and shorten time to treatment even with smaller DNA panels. An expansion study using comprehensive NGS plasma testing with faster turnaround time is ongoing (NCT04862924).

Publisher

SAGE Publications

Subject

Oncology

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