Annual screenings of patients at high risk for lung cancer can catch tumors early and improve a patient’s long-term prognosis. However, low-dose computer tomography (LDCT) has a high false-positive rate that can lead to unnecessary biopsies. University of Missouri School of Medicine researchers have found a blood biomarker that can complement LDCT by distinguishing non-small-cell lung cancer (NSCLC) from benign nodules without an invasive biopsy.
“It’s a simple blood test that checks for two things: circulating tumor cells (CTCs) that detach from a primary tumor and circulate in the blood, and tumor-macrophage fusion (TMF) cells that have been determined to be highly prognostic for poor survival after lung cancer surgery,” says study author Jussuf Kaifi, MD, a cancer surgeon at MU Health Care and an assistant professor of surgery at the MU School of Medicine.
Kaifi’s team collected blood samples from 221 patients, including 90 NSCLC patients, 74 high-risk screening patients with either no or benign nodules and 37 patients determined to have suspicious nodules detected by LDCT. Researchers also tested a control group of 20 people who had never smoked who were at low risk for lung cancer.
“When we collected the samples from the patients in our study, we found CTCs in all 90 patients with NSCLC, none of the patients in the control group, and in 29 of 37 patients with suspicious nodules,” Kaifi says. “We also found TMF cells in some NSCLC patients, and those were not present in patients with benign nodules.”
However, Kaifi’s team found that the rarity of TMF cells may make them unsuitable blood biomarkers for early cancer detection. Only 48% of patients with NSCLC tested positive for giant TMF cells. The next step is to conduct a prospective, large-scale, multicenter clinical trial to validate the role cellular liquid biomarkers play in improving diagnostic accuracy.
“This study demonstrated that integrating cellular liquid biomarkers, CTCs and TMF cells into standardized LDCT screening protocols can improve accuracy of NSCLC detection in high-risk patients who have nodules detected by LDCT,” Kaifi says. “This is a promising finding that can potentially improve the screening process, improve cancer outcomes and reduce unnecessary interventions and associated morbidities.”
In addition to Kaifi, the study authors include MU postdoctoral fellows Kanve Suvilesh, PhD, Yariswamy Manjunath, PhD, and Vijay Radhakrishnan, PhD; Jonathan Mitchem, MD, assistant professor of surgery; Eric Kimchi, MD, the John A. Growden Distinguished Professorship in Surgery; Kevin Staveley-O’Carroll, MD, professor of surgery; and Guangfu Li, PhD, assistant professor of surgery.
Their study, “Circulating Tumor-Macrophage Fusion Cells and Circulating Tumor Cells Complement Non-Small-Cell Lung Cancer Screeing in Patients With Suspicious Lung-Rads 4 Nodules,” was recently published by JCO Precision Oncology. Research reported in this publication was supported by an Ellis Fischel Cancer Center Pilot Award and funding from the Department of Veterans Affairs. The content is solely the responsibility of the authors and does not necessarily represent the official views of the funding agencies.