The excellent paper of Moadel and colleagues [1] gives further support to the findings reported earlier by Meyer and colleagues [2] suggesting that 18F-FDG may be of benefit in treating hyper-metabolic neoplasms. For small breast tumors in five mice injected with 18F-FDG (2–4 mCi, i.p.), Moadel and colleagues noted that 4% of tumor cells stained for an apoptotic marker 10 days afterward versus less than 1% of controls. For larger tumors in three older mice injected intra-peritoneally with 2 mCi of 18F-FDG, necrosis was found to comprise about 14% of the total tumor volume 10 days after the injection. However, as shown in the first known autoradiographic study of deoxyglucose uptake in breast cancer [3] (see Fig. 1), central necrotic areas could be identified which did not accumulate tracer and comprised approximately 12.5% of the estimated total tumor volume. As suggested by the detail seen in figure one, autoradiography of tracer doses of 18F-FDG in tissue sections would be an excellent way to test a response to radiotherapeutic doses of this tumor avid radiopharmaceutical, with the ability to simultaneously perform histochemical staining of apoptosis markers.
Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.