A slow-growing type of neuroendocrine tumor in the lungs.
Central
Neuroendocrine Tumor
Origin: Neuroendocrine
Grade: Low
Severity: Low
Molecular Marker: Chromogranin A
Age Range: 40-60 years
Life Expectancy: 5-10 years
Carcinoid tumors are a type of lung cancer classified under neuroendocrine tumors. These tumors originate in the hormone-producing neuroendocrine cells found throughout the body. When they occur in the lungs, they can be centrally located, typically within the bronchi.
Carcinoid tumors in the lungs may not cause symptoms initially. However, as they grow, they can lead to a variety of symptoms, including:
Surgery is often the primary treatment for localized carcinoid tumors in the lungs, especially if they are detected early. Surgical options include:
Radiation therapy is generally not the first line of treatment but can be used post-surgery or for symptom control in inoperable cases.
Research is ongoing to explore the efficacy of immunotherapy in treating carcinoid tumors. This approach involves stimulating the immune system to target and destroy cancer cells.
Targeted therapies that block specific molecules involved in tumor growth are under investigation. These include inhibitors targeting the mTOR pathway, which is involved in cell proliferation.
Patients may have the option to participate in clinical trials investigating new drugs, combinations of existing treatments, or novel therapeutic approaches.
Carcinoid tumors, a subtype of neuroendocrine tumors in the lung, can be effectively managed through a combination of surgical, medical, and experimental treatments. Continuous research and clinical trials are advancing the understanding and management of this disease, offering hope for more effective treatments with fewer side effects in the future.