An Oncologist Explains How She Uses ctDNA in Gastric Cancer

January 24, 2024
Brielle Benyon
Brielle Benyon

Brielle Benyon, Assistant Managing Editor for CURE®, has been with MJH Life Sciences since 2016. She has served as an editor on both CURE and its sister publication, Oncology Nursing News. Brielle is a graduate from The College of New Jersey. Outside of work, she enjoys spending time with family and friends, CrossFit and wishing she had the grace and confidence of her toddler-aged daughter.

Circulating tumor DNA can be a valuable tool in gastric cancer, but unanswered questions remain, an expert said.

Circulating tumor DNA (ctDNA), describes the cancer fragments that can be detected in a patient’s bloodstream. While the role of ctDNA has not definitively been outlined in the gastric cancer space, it can help guide treatment decisions.

At the 2024 Gastrointestinal Cancers Symposium, Dr. Sunnie Kim, a medical oncologist at UCHealth Cancer Care, Anschutz Medical Campus, University of Colorado Cancer Center, sat down and discussed how she uses ctDNA in treating patients with gastric or esophageal cancer.

READ MORE:Cancer in Bloodstream May Predict CRC Outcomes

Transcript

ctDNA technology is very promising in the field, although it's not fully validated at this time. There are a lot of clinical trials that are investigating how we can alter treatment based on the presence of a positive ctDNA or even a negative ctDNA results.

So ctDNA is circulating tumor DNA, and it can detect DNA cancer DNA at a level that scans may not be able to or more conventional cancer antigens in the blood may not be able to detect.

How I use it is really personalized based on each patient. So, say someone goes through neoadjuvant therapy for gastric or esophageal cancer but is very hesitant about going through surgery. But the scan shows that there's a radiologic complete response. Sometimes I'll use ctDNA there just to track what I think is going to be microscopic cancer in their body. If it stays negative or is at a very low level and statelet low level, I may not initiate more chemotherapy or immunotherapy. But if it slowly becomes positive over time, then I know I need to watch that patient more carefully doing scans on a more frequent basis, because I have a high suspicion that we're going to start seeing that that cancer on the scan for patients with advanced disease.

Sometimes I will also use ctDNA just to track certain mutations to see if over time we're seeing more of that mutation in the tumor and trying to tailor it to a more personalized treatment approach.


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