Tate (** - Lutathera (Lutetium Lu 177 dotatate) - Various radiopharmaceutical preparations **)
Other Medications
Description
Tate (Lutetium Lu 177 dotatate) is a type of medication being studied in clinical trials for certain cancers. It is currently being investigated as a potential treatment option for metastatic colorectal cancer (mCRC) that has not responded to other treatments (refractory mCRC). In the clinical trial NCT04701476, Tate is being used in combination with pembrolizumab (an immunotherapy drug) for patients with refractory mCRC. The goal of this trial is to see if this combination improves overall survival compared to standard treatments like regorafenib or TAS-102. Tate is administered via a procedure called Trans-arterial Tirapazamine Embolization (TATE). It is important to note that Tate is not yet approved for treating colorectal cancer.
Mechanism of Action
Tate is a radiopharmaceutical. It contains lutetium-177, a radioactive isotope, attached to dotatate, a molecule that targets specific receptors found on certain types of cancer cells, including neuroendocrine tumors. The dotatate part helps deliver the radiation directly to the tumor cells. The radiation emitted by lutetium-177 damages the DNA of the cancer cells, leading to their death. In the context of the NCT04701476 trial, Tate is being used in combination with pembrolizumab, which is an immunotherapy drug that helps the body's immune system fight cancer. The specific mechanism of Tate in the context of mCRC is being studied, as it is primarily known for targeting neuroendocrine tumors.
Side Effects
Not all side effects are listed. Side effects vary by individual. Always consult your oncologist.