Gene Solutions Thailand Exhibition & Symposium Highlight at TSCO Annual Meeting

Explore the highlights from our booth exhibition and symposium at the Thai Society of Clinical Oncology (TSCO) Annual Meeting, held from October 18-20, 2024, at Dusit Thani Pattaya, Thailand.

Gene Solutions team at the TSCO Annual Meeting 2024 exhibition booth showcasing ctDNA, Minimal Residual Disease (MRD), and precision oncology applications, attended by Thai Society of Clinical Oncology members and professionals in cancer research.

During Symposium 3, Gene Solutions presented an insightful session featuring Professor Nick Pavlakis from the University of Sydney and Dr. Tu Ngoc Ly Lan from the Medical Genetics Institute HCMC. They shared groundbreaking applications of Minimal Residual Disease (MRD) and discussed global clinical trials, showcasing the rapid advancements in circulating tumor DNA (ctDNA)-based testing.

Professor Pavlakis comprehensively reviewed all current aspects of ctDNA MRD, from technical approaches to clinical applications. In terms of technical strategies, he discussed two notable subjects: proven enrichment strategies using Hybridization Capture (NGS) or Multiplex PCR Amplification (NGS) to increase ctDNA sensitivity, and technical classifications to identify Clonal Hematopoiesis of Indeterminate Potential (CHIP), which has a mutational frequency of approximately 92% in 60-year-olds and can cause false positives.

Professor Nick Pavlakis discusses the applications of ctDNA in monitoring Minimal Residual Disease (MRD) at the TSCO Annual Meeting 2024, highlighting advances in lung and colorectal cancer treatment

In clinical applications, Professor Pavlakis highlighted multiple studies that provided compelling evidence of MRD:

  • Applications of ctDNA assay for MRD in early-stage curatively treated cancers: These applications vary from peri-operative prognostic and predictive uses, including escalation of adjuvant therapy (MRD+) in lung cancer, de-escalation/avoidance of adjuvant therapy (MRD-) in colorectal cancer, and surveillance/monitoring for recurrence.
  • One study in resected EGFRm stage IB-IIIA NSCLC: This study showed that patients receiving adjuvant osimertinib were more likely to be DFS and MRD event-free compared to those receiving a placebo.
  • One study in neoadjuvant chemotherapy in TNBC: ctDNA dynamics during neoadjuvant chemotherapy showed evidence in predicting clinical outcomes.
  • One recent study in CRC demonstrated that a ctDNA-informed approach to adjuvant therapy selection in stage II colon cancer can reduce chemotherapy use without compromising survival rates.

Dr. Tu Ngoc Ly Lan of Gene Solutions presents on genomic profiling and personalized cancer monitoring at the TSCO Annual Meeting 2024, focusing on the benefits of ctDNA-based monitoring

Dr. Tu Ngoc Ly Lan provided another perspective on current MRD methods, discussing the advantages and limitations of ctDNA and how to interpret its results. While it is widely acknowledged that ctDNA is more sensitive than conventional biomarkers and imaging in multiple cancers, she emphasized that no test detects ctDNA in 100% of cases. Detection rates can vary based on assay sensitivity, sample quality, and tumor location, particularly in cases with low ctDNA shedding, such as breast luminal cancer, lung adenocarcinoma, or metastatic sites in the brain, bone, and peritoneum.

The insights shared by the two experts enriched the audience’s overview of MRD, highlighting high-sensitivity methods and their application in clinical practice.

Symposium 3 at the TSCO Annual Meeting 2024 featuring discussions on ctDNA's role in monitoring Minimal Residual Disease, with speakers Dr. Tu Ngoc Ly Lan and Professor Nick Pavlakis

We deeply appreciate the organizers, moderators, speakers, and medical oncologists who participated in this cutting-edge sharing for the sake of better personalized cancer care.

#ctDNA #MRD # PrecisionOncology #Personalizedmonitoring #TSCO

LATEST News

New Study Validates Gene Solutions’ Upgraded ctDNA Workflow Behind K-TRACK and K-4CARE

New Study Validates Gene Solutions’ Upgraded ctDNA Workflow Behind K-TRACK and K-4CARE

Peer-reviewed findings published in The Journal of Liquid Biopsy, an official journal of the International Society of Liquid Biopsy (ISLB), demonstrate broader ctDNA analysis, improved recurrence prediction, and greater flexibility with or without tumor tissue. SINGAPORE, 14 October 2026 – Gene Solutions announced the publication of a new peer-reviewed study validating the upgraded ctDNA workflow behind K-TRACK, K-4CARE, and K-TRACK Blood Only. Published in The Journal of Liquid Biopsy, an official journal of the International Society of Liquid Biopsy (ISLB), the study evaluated how Gene Solutions’ new hybrid-capture sequencing workflow and VarSURE bioinformatics pipeline improve upon its previous amplicon-based ctDNA method.

Read More

Biomarker and ctDNA Testing: A Personalized Approach to Cancer Care

Cancer diagnosis often brings many questions: Which treatment is most suitable for me? Is my treatment working? Has cancer changed? Could it come back? Every person’s cancer is different. Even when two people have the same type of cancer, their tumors may have different biological features. These differences can influence how the cancer behaves and how it responds to treatment. Biomarker and circulating tumor DNA, or ctDNA, testing may help doctors better understand these differences. Together, these tests may support more personalized treatment decisions and provide additional information as the cancer changes over time. Why can the same cancer respond

Read More
Gene Solutions NIPT preterm birth prenatal health

Gene Solutions Study Finds Preterm-Birth Signals in Routine triSure NIPT Data

A Gene Solutions study published in American Journal of Obstetrics & Gynecology (AJOG) Global Reports finds cell-free DNA fragmentomic patterns associated with spontaneous preterm birth, pointing to a potential path toward earlier pregnancy-risk assessment. SINGAPORE, Sept. 25, 2026 /PRNewswire/ — Gene Solutions, a global biotechnology company providing precision cell-free DNA solutions through multi-omics and artificial intelligence to improve pregnancy care, cancer detection and precision medicine, today announced the publication of a study showing the potential to assess the risk of spontaneous preterm birth from cell-free DNA fragmentomic signals already present in routine first-trimester non-invasive prenatal testing (NIPT) data. Published in AJOG Global Reports, the

Read More