Novel tracer developed for precision targeting of non-small cell lung cancer

Researchers have developed a new nuclear medicine tracer that could improve diagnosis and treatment of non-small cell lung cancer. Research published in the November issue of The Journal of Nuclear Medicine found that the new tracer, ^99mTc-HYNIC-cMBP, produced clearer images in less time than currently used tracers and was more rapidly eliminated from the body, reducing radiation exposure.

The c-Met receptor—a promising therapeutic target for this disease—is a tyrosine kinase receptor that promotes the growth of cancer cells, particularly in NSCLC. When c-Met receptors are elevated, cells may be resistant to EGFR-targeted therapy. However, with precise targeting of the c-Met receptor, physicians may be able to more effectively treat this disease.

In the study, the novel radiotracer was developed and cultured in two NSCLC cell lines, H1993 (high c-Met expression) and H1299 (no c-Met expression), and the activity and uptake of the ^99mTc-HYNIC-cMBP tracer was assessed. These tumor cells were then transplanted into mice, and in vivo tumor specificity was measured by SPECT at various intervals after injection of the tracer. Blocking assays, biodistribution and autoradiography also were conducted to determine the tracer’s specificity.

The authors found the preparation of the ^99mTc-HYNIC-cMBP imaging agent to be simple, providing a high yield of the tracer with few associated costs. Biodistribution and autoradiography showed significantly higher accumulation of 99mTc-HYNICcMBP in H1993 tumors than in H1299 tumors. In addition, the H1993 tumors were clearly visualized after only a half hour in SPECT images, while the H1299 tumors were not observed at any time. The tracer was also cleared rapidly, which is favorable for reducing exposure to radiation, background noise and long delays between treatment and imaging readout.

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