Cytalux is designed to improve the ability to locate additional lung cancerous tissue that are normally difficult to detect during surgery. The drug is a diagnostic agent that is administered in the form of an intravenous injection prior to surgery.
FDA approved Cytalux in November 2021 for identifying ovarian cancer lesions.
Disease or Condition
The American Cancer Society External Link Disclaimer estimates there will be more than 236,000 new cases of lung cancer and more than 130,000 deaths from this disease in 2022, making it the deadliest of all cancers. Conventional treatment for lung cancer includes surgery to remove as many of the tumors as possible, chemotherapy to stop the growth of malignant cells or other targeted therapy to identify and attack specific cancer cells.
The safety and effectiveness of Cytalux was evaluated in a randomized, multicenter, open-label study (NCT04241315) of patients with known or suspected lung cancer who were scheduled to undergo surgery. Of the 110 patients who received a dose of Cytalux and were evaluated under both normal and fluorescent light during surgery, 24% had at least one cancerous lesion detected that was not observed by standard visual or tactile inspection.
The most common side effects of Cytalux were infusion-related reactions, including nausea, vomiting, abdominal pain, flushing, dyspepsia, chest discomfort, itching and hypersensitivity. Cytalux may cause fetal harm when administered to a pregnant woman. The use of folate, folic acid, or folate-containing supplements should be avoided within 48 hours before administration of Cytalux. There is a risk of image interpretation errors with the use of Cytalux to detect lung cancer during surgery, including false negatives and false positives.
Cytalux received priority review designation for this indication.
FDA granted this supplement approval to On Target Laboratories, LLC.