Tissue biopsy means taking a small piece of a tumor, usually by surgery or using a needle, to study it at the molecular level. This method uses next-generation sequencing (NGS) to find genetic changes like mutations and gene fusions in cancer cells. Examining tumor DNA helps doctors pick treatments that target those specific changes in the cancer.
But tissue biopsy has some drawbacks. It needs an invasive procedure that can be risky or hard depending on where the tumor is. Also, tissue samples only show one part of the tumor, so they might miss differences within the tumor since tumors can be uneven inside. It can also take a long time to get and test the sample, delaying treatment for the patient.
These issues show the need for other tests that are less invasive and faster while providing detailed molecular information.
Liquid biopsy is a newer method that tests materials from the tumor found in blood plasma. These materials include circulating tumor DNA (ctDNA) and cell-free RNA (cfRNA) released by tumors into the blood. Unlike tissue biopsy, liquid biopsy needs only a blood draw, so it is less invasive and safer for patients.
Liquid biopsy helps tissue genotyping in many ways:
Non-small cell lung cancer (NSCLC) is the main type of cancer where liquid biopsy has been studied a lot. Research shows that doctors used liquid biopsy results to decide front-line treatments in 73.5% of cases, while tissue biopsy data was used in only 25.9%. Tests for important biomarkers matched between liquid and tissue biopsy from 94.8% to 100% of the time. This shows liquid biopsy is a reliable alternative or addition to tissue genotyping to find treatable mutations.
Also, a liquid-first testing method found actionable biomarkers in 76.5% of patients versus 54.9% with tissue-first testing. This means using liquid biopsy can help more patients get targeted therapies and qualify for clinical trials.
Organizations like the National Comprehensive Cancer Network (NCCN) now include liquid biopsy as part of the recommended testing for NSCLC. Liquid biopsy is also being used more with other solid tumors to guide treatments based on molecular profiles.
Despite its benefits, liquid biopsy has some challenges. It relies on enough tumor DNA entering the blood, which may be low in some tumors, like slow-growing ones or cancers in the brain. This can cause false-negative results. Another issue is clonal hematopoiesis of indeterminate potential (CHIP), where mutations from blood cells can appear and confuse results.
Test accuracy can differ, so there is a need to standardize methods across labs and patient groups. The cost is also being studied, with hopes that falling prices for sequencing will make it easier to use.
Research and technology efforts are ongoing to solve these problems. Better bioinformatics, sequencing tools, and sample methods are improving test quality and consistency.
Companies like Tempus show how big data and AI platforms improve cancer care. Tempus connects about 65% of US Academic Medical Centers and more than half of US oncologists with its precision medicine platform. This system combines clinical and molecular data to help doctors and researchers.
Tempus manages a lot of data—about 350 petabytes—including over 8 million anonymous research records. This huge data helps create algorithms that find targeted treatments, predict how well treatments will work, and match patients to clinical trials.
Partnerships between hospitals, research centers, and AI companies make it easier to offer complete molecular profiling using both tissue and liquid biopsies. Tools like Tempus One, an AI clinical assistant inside electronic health records (EHR), improve workflows and decision-making. This reduces some administrative work for healthcare staff.
Good molecular profiling needs advanced data analysis and smooth clinical processes. Artificial intelligence (AI) is growing in use by automating data handling, pattern recognition, and treatment ideas.
AI looks at large sets of genetic and clinical data to find important mutations and suggest personalized treatments. For example, Tempus One helps doctors use EHR data easily and build custom workflows to save time.
Automation can also track sample status, give priority to urgent cases, and alert staff about missing or incorrect data without manual checking. This reduces delays common in molecular testing.
Simbo AI is an example of a company that uses AI for phone automation in clinical settings. Its system manages patient calls, schedules appointments, and answers routine questions using natural language processing. This lets medical staff spend more time on patient care instead of administrative tasks.
Together, AI tools and workflow automation make cancer centers work more smoothly and deliver better care.
Healthcare leaders should think about adding liquid biopsy to their cancer molecular profiling programs. Some key points include:
In the US, many Academic Medical Centers and oncologists already use AI platforms. Practices that add liquid biopsy and AI tools will likely keep up with advances and improve cancer care.
Combining liquid biopsy with traditional tissue genotyping has made cancer molecular profiling more complete and faster. For NSCLC and other cancers, liquid biopsy gives less invasive, quicker, and often more detailed genetic data that complements tissue analysis. With high agreement to tissue tests, shorter turnaround times, and the ability to monitor tumors in real time, liquid biopsy is an important tool.
New AI and automation technologies also improve how molecular profiling works, helping doctors handle more complex data efficiently. Companies like Tempus show how integrated data and AI support personalized cancer treatment.
For healthcare administrators, owners, and IT managers in the United States, using liquid biopsy as part of a full molecular profiling program with AI support can help improve patient care, make operations smoother, and stay up to date with current cancer treatment methods.
AI accelerates the discovery of novel targets, predicts treatment effectiveness, identifies life-saving clinical trials, and diagnoses multiple diseases earlier, enhancing personalized patient care through advanced data analysis and algorithmic insights.
Tempus provides an AI-enabled assistant that helps physicians make more informed treatment decisions by analyzing multimodal real-world data and identifying personalized therapy options.
Tempus supports pharmaceutical and biotech companies with AI-driven drug development, leveraging extensive molecular profiling, clinical data integration, and algorithmic models to optimize therapeutic strategies.
The xT Platform combines molecular profiling with clinical data to identify targeted therapies and clinical trials, outperforming tumor-only DNA panel tests by using paired tumor/normal plus transcriptome sequencing.
It uses neural-network-based, high-throughput drug assays with light-microscopy to predict patient-specific drug response heterogeneity across various solid cancers, improving treatment personalization.
Liquid biopsy assays complement tissue genotyping by detecting actionable variants that might be missed otherwise, providing a more comprehensive molecular and clinical profiling for patients.
~65% of US Academic Medical Centers and over 50% of US oncologists are connected to Tempus, enabling wide adoption of AI-powered sequencing, clinical trial matching, and research partnerships.
Tempus One is an AI-enabled clinical assistant integrated into the Electronic Health Record (EHR) system, allowing custom query agents to maximize workflow efficiency and streamline access to patient data.
xM is a liquid biopsy assay designed to monitor molecular response to immune-checkpoint inhibitor therapy in advanced solid tumors, offering real-time treatment response assessment.
Fuses combines Tempus’ proprietary datasets and machine learning to build the largest diagnostic platform, generating AI-driven insights and providing physicians a comprehensive suite of algorithmic tests for precision medicine.