While tissue biopsy remains the gold standard for disease diagnosis and research, interest in liquid biopsy as an alternative or adjunct to tissue sampling is increasing. Presently, experts are actively exploring liquid biopsy in precision medicine for cancer detection, screening for disease recurrence, evaluating treatment response, and assessing residual disease at the molecular levels.
With tissue biopsy, nucleic acids and proteins can be assessed in situ, along with their architectural and spatial context. However, tissue sampling is invasive, not amenable to repetition and might be technically challenging or associated with unacceptable procedural risks. Further, in clinical studies, a requirement for multiple biopsies significantly slows down enrollment rate due to high patient burden. When tumor tissue sampling is not feasible, liquid biopsy offers a minimally invasive alternative. Liquid biopsy also enables serial testing across multiple timepoints, which could be used for longitudinal monitoring of whole-body disease burden, tumor progression or therapeutic response.
Cancer, as a spatially and temporally dynamic disease, demonstrates heterogeneity not just within tumors, but also between primary and metastatic tumors in the context of precision medicine. Consequently, single tissue biopsies may lead to drastic underestimation of the full genomics landscape of an individual patient’s cancer.[1] Thus, liquid biopsy can serve to complement traditional tissue-based assays, providing additional or adjunctive insights.
In this article, we investigate the two main genomics-based methods in liquid biopsy: analysis of circulating DNA/RNA and circulating tumor cells (CTCs), examining their advantages, drawbacks, and possible applications in precision medicine.
Certain liquid biopsy techniques in precision medicine examine circulating nucleic acids, encompassing both DNA and RNA. Circulating nucleic acids comprise both circulating tumor DNA and RNA (ctDNA and ctRNA) and cell-free DNA and RNA (cfDNA and ctRNA). Studies have revealed that ctDNA, or tumor-derived DNA fragments unassociated with cells, accurately represents the tumor's origin, making it valuable in liquid biopsy for precision medicine. A study comparing targeted sequencing of ctDNA and matched tissue biopsies from patients with metastatic castration-resistant prostate cancer (mCRPC) showed high concordance in the gene alterations identified.[2]
Meanwhile, cfDNA and cfRNA describe any nucleic acids that are circulating in the bloodstream but are not necessarily of tumor origin. Cancer patients typically exhibit higher average cfDNA levels compared to healthy individuals, and numerous studies in liquid biopsy research have shown a strong correlation between mutations identified in cfDNA and those discovered in tissue biopsy samples.[3] There is also evidence that levels of plasma cfDNA increase as tumors progress and that cfDNA acts as a signaling molecule to induce metastasis.[4] In addition, recent research focused on cfDNA methylation signatures and fragmentation patterns demonstrates promise for screening, early detection, and monitoring of cancer. Moreover, accumulating knowledge indicates that non-coding circulating RNAs play a critical role in the pathogenesis of various cancers and that dysregulated microRNA expression levels may be useful as clinical biomarkers.[5]
Genomic profiling of circulating DNA is generally performed using digital droplet PCR (ddPCR) if the researchers has identified a gene mutation of interest or NGS if the mutation of interest has not yet been delineated. Sequencing of ctDNA generates a large volume of information, including the mutation status of dozens or hundreds of oncogenes simultaneously. However, key limitations of ctDNA are that it does not provide any information on the expression levels of any given protein or any exon-skipping events or splice variants and that its clinical utility for primary cancer screening and minimal residual disease (MRD) monitoring remains unproven.[6]
In the last decade, advancements in isolating circulating tumor cells (CTCs) have enabled single-cell level analysis, allowing researchers to study spatial and temporal dynamics in circulation within liquid biopsy and precision medicine.[7] A growing body of evidence demonstrates that CTCs—cancer cells that have migrated into the bloodstream—undergo dynamic molecular changes in response to systemic therapy and may have clinical utility as functional biomarkers. In metastatic breast cancer, prevalence of CTCs in the blood has been correlated with lower progression-free and overall survival and has been shown to be of higher prognostic value than conventional imaging.[8],[9]
CTC-based liquid biopsies have the advantage of preserving cellular contents, allowing for gene expression profiling and other downstream analyses at the single cell level. In addition, tumors may harbor segregated clones, which could easily be missed by biopsy but may be captured by CTCs. Moreover, target biomarkers on the surface of CTCs can easily be identified with simple antibody binding, as long as the respective antibody is available.
| Advantages | Limitations | |
| Circulating DNA | Technically easier to isolate than CTCs High sensitivity and dynamic range May be representative of intratumor heterogeneity No requirement for enrichment prior to analysis | Not all DNA mutations may be expressed Treatment-related leukocyte and erythrocyte apoptosis could spike ctDNA fraction, thus not reflecting cancer cell death Source of DNA may not be clear Large background of normal cfDNA Unknown whether ctDNA is released from cancer cells because they are dying from or resistant to therapy Certain medical conditions may cause elevation of circulating DNA |
| Circulating Tumor Cells | Cells, not nucleic acids, are the functional unit driving disease biology May be representative of intratumor heterogeneity May be better than circulating DNA for discovering novel targets and evaluating the frequency of multiple known targets Intact cells could be resistant clones Can be used for functional assays (e.g., DNA, RNA, protein) Can be cultured to evaluated drug resistance both in vitro and in vivo | May be more difficult to isolate than circulating DNA Detection is complicated by potentially dynamic marker expression, as is seen with CTCs undergoing epithelial-to-mesenchymal transition (EMT)[11] Sampling bias of captured cells if selection is affinity- or size-based |
Genomics-based liquid biopsy offers extensive potential in various oncology applications, from deciphering a drug's mechanism of action to categorizing patients and tracking treatment response in precision medicine. Currently, most of the FDA-approved liquid biopsy clinical diagnostics use ctDNA or cfDNA. In 2020, two companion diagnostics (CDx) that combine liquid biopsy and next-generation sequencing (NGS) were approved, demonstrating the feasibility and utility of targeting multiple genes to guide clinical decision-making.
cfDNA, extensively researched in various cancer types within precision medicine, shows potential as a tool for cancer detection, tumor mutation assessment, treatment eligibility determination, tumor dynamics and therapy response monitoring, and overall survival prediction.[12] In a secondary analysis of the BOLERO-2 clinical trial, prevalence of ESR1 mutations in cfDNA was inversely correlated with overall survival.[13] Numerous studies have demonstrated ctDNA can be used for minimal residual disease (MRD) detection and monitoring after treatment, which aids in assessing response, prognosis, and risk of recurrence.[14] Circulating DNA has also been explored extensively as a tool for providing early assessments of response to immune checkpoint inhibitor therapy.[15]
CTCs have a wide range of applications, from evaluating pharmacodynamic or mechanistic markers and establishing dosing strategies to characterizing heterogeneous CTC subpopulations and selecting patients for clinical trial enrollment. They can also be used as prognostic or predictive biomarkers. For example, in mCRPC, a high degree of phenotypic heterogeneity in CTCs is linked to decreased overall survival.[16] Further, in a small study of patients with pancreatic cancer, researchers found that a sufficient number of CTCs could be obtained from 10 ml of anticoagulated blood to allow for multiparameter phenotyping using qualitative immunofluorescence to identify features that could potentially serve as selective, predictive, or prognostic biomarkers.[17]
Interrogating CTC biomarkers may also be useful for predicting or monitoring treatment response. For example, in the BEACON trial, multiplex immunofluorescence (mIF) was performed on CTCs isolated from patients with metastatic breast cancer treated with etirinotecan pegol (EP) to measure expression of potential response biomarkers. It was found that topoisomerase (Top1) expression might be useful for identifying those patients who were most likely to experience an overall survival benefit with EP treatment.[18]
Another potential application of CTCs is in patient selection for clinical trials of solid tumor CAR-T cell therapy and other targeted therapeutics. Typically, patients would be stratified using immunohistochemistry (IHC), but if tissue biopsy is not possible, testing CTCs for the target biomarker would be an alternative approach to making enrollment decisions.
Circulating DNA and CTCs circulate at low frequencies. To generate clinically meaningful information, isolation and enrichment of the nucleic acid or cell of interest is generally required. ApoStream, Precision for Medicine’s proprietary CTC platform, uses a dielectrophoresis-based, antibody-independent separation approach to isolate and enrich CTCs. This technology can also be used to isolate other rare cell types such as stem cells, CAR-T cells, and other difficult-to-identify immune cell populations. With ApoStream, enriched cells remain intact and can be integrated with any downstream assay, including mIF, NGS, fluorescence in situ hybridization (FISH) and ISH (see Figure 1).
Liquid biopsy holds great potential for the diagnosis, treatment, and monitoring of patients with cancer. Circulating DNA and circulating tumor cells (CTCs) are both expected to have complementary functions as cancer biomarkers in precision medicine, potentially working together to inform clinical decisions. As technology continues to advance, the clinical applications of liquid biopsy in precision medicine will keep growing, extending beyond oncology to various therapeutic areas.
Discover how Precision for Medicine supports researchers in obtaining molecular insights through liquid biopsy in precision medicine by clicking here.
Jesus Garcia, PhD, is a tissue and liquid biopsy expert with extensive experience in a wide range of histopathology assays and digital pathology solutions. Part of the implementation of new technologies at MD Anderson Cancer Center in collaboration with immuno-oncology leaders. Currently focused on partnering with biopharma to develop tissue and liquid biopsy biomarker strategies for clinical trials, and to implement digital pathology and AI in the drug development process.
Precision for Medicine is part of the Precision Medicine Group, an integrated team of experts that extends Precision for Medicine’s therapeutic development capabilities beyond approval and into launch strategies, marketing communication, and payer insights. As one company, the Precision Medicine Group helps pharmaceutical and life-sciences clients conquer product development and commercialization challenges in a rapidly evolving environment.
