Liquid biopsy means taking a small sample of blood to find and measure parts of cancer that float in the blood. These parts include circulating tumor cells (CTCs), circulating tumor DNA (ctDNA), extracellular vesicles (EVs), and microRNAs (miRNA). Unlike regular tissue biopsy that removes tissue through surgery, liquid biopsy is less painful and can give information about the tumor’s changes and how it reacts to treatment at any time.
This method has changed a lot over the past ten years. Doctors now use it mostly for cancers like lung and breast cancer. In the United States, liquid biopsy helps doctors watch how well treatments are working, find if any cancer remains after treatment, and choose therapies that target certain changes in tumors.
Because patients can give blood samples often without much discomfort or danger, doctors can make better and faster treatment choices. This is very helpful for patients using immune-checkpoint inhibitor therapy, where the response can be hard to judge because the immune system is involved in fighting the cancer.
Together, these markers let doctors understand the tumor better and keep track of changes. This gives more information than just one tissue biopsy test.
Several new technologies have made liquid biopsy tests more accurate and useful in clinics:
Using these technologies together helps doctors get better molecular profiles of tumors and check how they respond to treatments in real time.
Artificial Intelligence (AI) is important in checking large amounts of data produced by liquid biopsy tests. AI systems that combine genetic, RNA, and protein data help doctors understand complex tumor biology.
AI can recognize patterns and predict how a tumor might respond or resist treatment. This helps doctors choose the best immune-checkpoint inhibitors based on current molecular information.
For hospitals and clinics treating many cancer patients, AI supports doctors and staff by creating automatic reports and alerts. This reduces the work needed to study and report data manually.
Immune-checkpoint inhibitors have changed cancer treatment, especially for cancers like lung, melanoma, and bladder cancer. These drugs boost the immune system’s ability to find and kill cancer cells by blocking certain pathways like PD-1/PD-L1 and CTLA-4.
Even though these drugs work well, patients react in many different ways, and normal scans may not show early changes. Liquid biopsy offers a non-invasive way to monitor how patients respond by checking ctDNA and CTC levels.
New liquid biopsy tests can track how tumors respond to immune therapies in real time. For example, some tests measure parts linked to the immune response and tumor changes. This helps doctors spot early signs of treatment not working and change therapy at the right time.
This shows that healthcare providers and researchers in the U.S. rely more on advanced liquid biopsy tests to improve cancer treatments.
Medical administrators and IT managers need to think about several things when adding liquid biopsy to clinical work:
By handling these points well, health organizations can better use liquid biopsy to monitor immune-checkpoint inhibitor treatments and improve patient results.
AI is not only used to analyze data. It also helps automate workflows, which is important for clinics giving advanced cancer care in the U.S.
IT managers need to work with clinical teams to create easy-to-use systems, keep data private, and ensure the technology works well.
There are still challenges in using liquid biopsy tests regularly for cancer care:
Medical administrators must think about these issues and work with vendors, insurers, and regulators to make sure liquid biopsy services can be offered and maintained.
As these improvements continue, liquid biopsy is expected to become a common tool in U.S. cancer care. It will help guide advanced tumor treatments, improve monitoring, and support better patient care.
Liquid biopsy tests have improved cancer diagnosis and treatment monitoring in the U.S. They provide a less invasive way to get current molecular information. These tests support immune-checkpoint inhibitor therapies and precision medicine.
Using AI and automation tools makes these tests more useful and efficient. They have become important tools for medical administrators, owners, and IT managers who want to improve cancer care.
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.