Blood Test Reveals Who Benefits from New Immunotherapy
- - Researchers at teh Mass General Brigham Cancer Institute in the United States have identified a specific marker in circulating tumor cells that predicts whether a patient with...
- The findings, published in 'Cancer Revelation', could allow doctors to easily and non-invasively determine which patients should receive the drug.
- The blood cell enrichment technology has been licensed to TellBio.
New Blood Test Predicts Response to Lung Cancer Immunotherapy
MADRID, 19 Jan. – Researchers at teh Mass General Brigham Cancer Institute in the United States have identified a specific marker in circulating tumor cells that predicts whether a patient with lung cancer will experience a lasting response to a recently approved immunotherapy drug called tarlatamab.
The findings, published in ‘Cancer Revelation’, could allow doctors to easily and non-invasively determine which patients should receive the drug.
“Isolating cancer cells from the blood has enormous potential to guide cancer therapies related to the immune system, and our group has created state-of-the-art bioengineering technologies for the purification of these circulating tumor cells,” says Dr. Daniel A. Haber,lead and corresponding author,and director of the Krantz Family Center for Cancer Research at the Brigham. “We’ve learned a lot about the biology of these cells, but we hadn’t had a test with direct clinical relevance. In this study, we believe we’ve achieved that.”
The blood cell enrichment technology has been licensed to TellBio.
The study focused on whether the properties of circulating tumor cells could correlate with a patient’s response to tarlatamab, which received full approval in late 2025 as a treatment for small cell lung cancer (SCLC) following prior chemotherapy. Tarlatamab is an antibody that recruits T cells to cancer cells expressing a specific neuroendocrine marker called DLL3.
While tarlatamab showed promising results in clinical trials, approximately half of patients with SCLC experience cancer progression within six months of starting treatment. It was previously believed that all cases of SCLC expressed DLL3, but Dr. Haber and his colleagues discovered that onyl half of the 20 patients studied had abundant DLL3-positive cancer cells in their blood – and these were the patients who responded to tarlatamab.
Testing for DLL3 in CTCs correctly identified 85% of patients who experienced a clinical benefit from the drug and 100% of those who did not (85% sensitivity, 100% specificity).
The study, a collaboration between bioengineers who developed the technology to analyze rare cancer cells in blood samples and lung cancer specialists, has significant implications for clinical care.
“Our work could help predict which patients with SCLC are likely to respond to tarlatamab and possibly other antibodies targeting DLL3,many of which are in advancement,” says dr. Justin Gainor, co-author of the study and director of the Thoracic Cancer Center Program at the Brigham. “It also has potential implications for other cancers that express DLL3 as they become more aggressive and for the field of antibody-directed cancer therapies.”
