Liquid Biopsy Lung Cancer Screening Method Developed
|
By LabMedica International staff writers Posted on 09 Apr 2020 |

Image: Histological sections of a moderately well differentiated squamous cell carcinoma of the lung showing infiltrating sheets and tongues of malignant squamous cells with whorls of keratin (Photo courtesy of Department of Health Western Australia).
Genomic blood tests for cancer screening and early detection have become the focus of attention in the molecular diagnostic space, though most activity so far has been either toward pan-cancer screening tools, or in a few other specific tumor types like colorectal cancer, where tests hope to vie against colonoscopy and existing stool-based methods.
Radiologic screening of high-risk adults reduces lung-cancer-related mortality; however, a small minority of eligible individuals undergo such screening in the USA. The availability of blood-based tests could increase screening uptake. A novel circulating tumor DNA (ctDNA) detection assay has been developed that could help physicians screen individuals at risk for lung cancer.
A large team of scientists at Stanford University (Stanford, CA, USA) and their colleagues have described a method, called Lung-CLiP (lung cancer likelihood in plasma), involves targeted sequencing of cell-free DNA (cfDNA) from plasma and matched white blood cell DNA to assess copy number and single nucleotide variants, coupled with a machine learning model that estimates the probability that a cfDNA mutation is tumor-derived. The estimate is based on biological and technical features specific to each variant, such as background frequency, cfDNA fragment size, the gene affected, and the likelihood of clonal hematopoiesis.
The team first trained and optimized Lung-CLiP in an initial sample of 104 patients with early stage non-small cell lung cancer and 56 matched controls. When they then applied it to an independent set of validation samples (46 cases and 48 risk-matched controls), the test was able to discriminate early-stage lung cancer patients with sensitivity and specificity levels that the authors believe suggest a significant benefit to the clinic: depending on where they set their specificity threshold, the method could achieve 63% sensitivity for stage I tumors and up to 75% sensitivity in detecting patients with stage III disease. Setting their cutoff at 98% specificity, the investigators found that Lung-CLiP detected 41% of patients with stage I disease, 54% of patients with stage II disease and 67% of those with stage III disease.
Ash Alizadeh, MD, PhD, an associate professor of Oncology and a senior author of the study, said, “Lung-CLiP could help increase the rate of early detection. This would be analogous to how stool-based testing proposes to improve screening for colorectal cancers, especially in populations where adoption of colonoscopy is lower than currently recommended.” The study was published on March 25, 2020 in the journal Nature.
Related Links:
Stanford University
Radiologic screening of high-risk adults reduces lung-cancer-related mortality; however, a small minority of eligible individuals undergo such screening in the USA. The availability of blood-based tests could increase screening uptake. A novel circulating tumor DNA (ctDNA) detection assay has been developed that could help physicians screen individuals at risk for lung cancer.
A large team of scientists at Stanford University (Stanford, CA, USA) and their colleagues have described a method, called Lung-CLiP (lung cancer likelihood in plasma), involves targeted sequencing of cell-free DNA (cfDNA) from plasma and matched white blood cell DNA to assess copy number and single nucleotide variants, coupled with a machine learning model that estimates the probability that a cfDNA mutation is tumor-derived. The estimate is based on biological and technical features specific to each variant, such as background frequency, cfDNA fragment size, the gene affected, and the likelihood of clonal hematopoiesis.
The team first trained and optimized Lung-CLiP in an initial sample of 104 patients with early stage non-small cell lung cancer and 56 matched controls. When they then applied it to an independent set of validation samples (46 cases and 48 risk-matched controls), the test was able to discriminate early-stage lung cancer patients with sensitivity and specificity levels that the authors believe suggest a significant benefit to the clinic: depending on where they set their specificity threshold, the method could achieve 63% sensitivity for stage I tumors and up to 75% sensitivity in detecting patients with stage III disease. Setting their cutoff at 98% specificity, the investigators found that Lung-CLiP detected 41% of patients with stage I disease, 54% of patients with stage II disease and 67% of those with stage III disease.
Ash Alizadeh, MD, PhD, an associate professor of Oncology and a senior author of the study, said, “Lung-CLiP could help increase the rate of early detection. This would be analogous to how stool-based testing proposes to improve screening for colorectal cancers, especially in populations where adoption of colonoscopy is lower than currently recommended.” The study was published on March 25, 2020 in the journal Nature.
Related Links:
Stanford University
Latest Pathology News
- AI Pathology Tool Predicts Relapse Risk in Stage II Colorectal Cancer
- AI Pathology Tool Stratifies Rectal Cancer to Guide Chemoradiotherapy
- PD-L1 Assay Guides Pembrolizumab Eligibility in Ovarian, Fallopian Tube, and Peritoneal Cancers
- AI Digital Pathology Platform Standardizes IHC Scoring in Breast Cancer
- AI Bone Marrow Mapping Provides New Tool to Track Blood Cancer Severity
- Digital Pathology Tool Predicts Breast Cancer Outcomes and Therapy Response
- AI Tissue Imaging Helps Guide Targeted Therapy for Lung Cancer
- Imaging Platform Maps Lipid Accumulations in Fabry Heart Tissue
- Tissue-Based Gene Signature Signals Colorectal Cancer Recurrence Risk
- FDA-Approved Companion Diagnostic Detects PTEN Loss in Prostate Cancer
- New AI Test Delivers Rapid Breast Cancer Recurrence Predictions
- EBV Status Helps Predict Survival in Primary CNS Lymphoma
- AI Pathology Tool Predicts Immunotherapy Response in Rare Cancers
- Uncertainty-Aware AI Tool Improves Digital Pathology for Cancer Subtyping
- Study Highlights Biomarker Testing Delays in Lung Cancer Care
- Stain-Free Imaging Platform Matches Standard Cancer Pathology
Channels
Clinical Chemistry
view channel
Blood Test Enters UK Primary Care Pathway for Earlier Alzheimer’s Diagnosis
Alzheimer’s disease is often first suspected in primary care, yet definitive evaluation frequently depends on specialized imaging or cerebrospinal fluid testing. This creates a persistent gap between disease... Read more
Machine Learning Model Shows Promise for Improving Metanephrine Testing Accuracy
Pheochromocytomas and paragangliomas are rare tumors that form in or near the adrenal glands and cause overproduction of stress hormones. Plasma-free metanephrines are the recommended first-line test,... Read moreHematology
view channel
Age-Specific CBC Reference Intervals Support Pediatric Diagnosis in Vietnam
Complete blood count (CBC) results underpin pediatric evaluation for anemia, infection, inflammation, and platelet disorders. Yet laboratories in Vietnam have largely relied on reference intervals derived... Read more
Spectral Flow Cytometry Assay Enhances MRD Detection in Multiple Myeloma
Minimal residual disease (MRD) monitoring is pivotal in multiple myeloma, where persistent malignant plasma cells drive relapse risk and help guide therapy decisions. In the United States, approximately... Read moreImmunology
view channel
Study Reveals Immune Mechanism Driving Severe COVID-19 Progression
Severe COVID-19 has highlighted gaps in understanding of early antiviral responses, particularly why some patients deteriorate despite timely care. Type I interferons are central to host defense, yet their... Read more
Antibody Profiling Identifies Preclinical Inflammatory Bowel Disease Years Before Diagnosis
Inflammatory bowel disease often develops after a prolonged symptom-free period, complicating timely recognition and clinical intervention. Limited understanding of immune activity during this silent phase... Read more
Ultrasensitive Blood Test Detects Sjögren’s Signature Years Before Diagnosis
Sjögren’s disease is a common autoimmune condition that can be difficult to recognize early, leading to delayed diagnosis and persistent symptom burden. It affects around half a million people in the UK... Read more
New Assays Expand Cytokine Testing for Transplant and Immunocompromised Patients
Eurofins Viracor has introduced three plasma-based assays—CXCL9 (Test Code 33607), CXCL10 (Test Code 33609), and interleukin-18 (IL-18) (Test Code 33611)—expanding its immunology testing menu for transplant... Read moreMicrobiology
view channel
Portable Molecular Platform to Advance Point-of-Care Testing for Lassa Fever
Lassa fever remains a persistent public health threat in West Africa, causing an estimated 100,000–300,000 infections annually and high case fatality rates among hospitalized patients. Clinical management... Read more
Study Highlights Need for Routine Hepatitis E Testing in Cirrhosis
Hepatitis E virus is a leading cause of acute viral hepatitis globally, yet infections often go unnoticed in healthy individuals. For patients with preexisting liver damage, however, infection can trigger... Read morePathology
view channel
AI Pathology Tool Predicts Relapse Risk in Stage II Colorectal Cancer
Bowel cancer is Australia’s fourth most commonly diagnosed cancer and the second leading cause of cancer death, while remaining the third most common cancer worldwide. In stage-two disease, determining... Read more
AI Pathology Tool Stratifies Rectal Cancer to Guide Chemoradiotherapy
Choosing intensified regimens for locally advanced rectal cancer is challenging because these therapies can cause serious side effects. Colorectal cancer is the fourth-most fatal cancer in the UK, and... Read more
PD-L1 Assay Guides Pembrolizumab Eligibility in Ovarian, Fallopian Tube, and Peritoneal Cancers
Agilent Technologies’ PD-L1 IHC 22C3 pharmDx (Code SK006) has received European Union certification as a companion diagnostic to aid in identifying patients with epithelial ovarian, fallopian tube, or... Read moreTechnology
view channel
Interoperable Data Platform Standardizes Multi-Cancer Blood Test Results
Proteotype Diagnostics has introduced Alchemi, a proprietary data and clinical workflow platform being developed for Enlighten, the company’s investigational blood-based multi-cancer test.... Read more
Training Device Improves Accuracy of Pooled Molecular Diagnostics
High-throughput molecular diagnostics have transformed infectious disease detection, but many workflows remain difficult to execute accurately without extensive training. Sample pooling can cut per‑test... Read more
New CE-Certified Software Advances Whole-Genome Cancer Testing
European hospitals are increasingly using comprehensive tumor genomics to guide therapy, but routine whole genome sequencing (WGS) requires validated, regulation-compliant workflows. A newly CE-certified... Read more
National Rare Disease Registry Standardizes Genetic and Clinical Data for Coordinated Care
Rare diseases collectively impose a significant clinical burden despite their individual rarity, often involving multisystem presentations and prolonged diagnostic journeys. Limited specialist expertise... Read moreIndustry
view channel







