Lung cancer is the third most common cancer in the UK. About 47,000 people are diagnosed with it each year. The lungs are the parts of the body that we use to breathe.
There are two main types of primary lung cancer. These are:
Sometimes cancer spreads to the lungs from somewhere else in the body. This is called secondary lung cancer.
We also have information about cancer that affects the lining that covers the lungs (the pleura). This is called mesothelioma.
There are some rarer types of cancers that can start in the lung. They include neuroendocrine tumours. These are sometimes called carcinoid tumours.
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Smoking tobacco is the cause of most lung cancers and the biggest risk factor. This includes smoking cigarettes, cigars and pipes. People who do not smoke can still develop lung cancer, but their risk is much lower.
If someone stops smoking, their risk of developing lung cancer gets lower over time. After about 15 years it is almost the same as a non-smoker.
Lung cancer is also more common in older people.
We have more information about the risk factors of lung cancer.
People may be diagnosed with lung cancer after seeing their GP about their symptoms. If your GP thinks your symptoms could be caused by lung cancer, they will arrange tests to help make a diagnosis. These can include:
If these tests show anything abnormal, your GP will refer you to a chest specialist within 2 weeks. Sometimes they will do this before getting the result of the chest x-ray.
At the hospital, the specialist will explain any other tests you need. These may include:
During a biopsy, a doctor or nurse takes samples of cells or tissue from the abnormal area. They look at the biopsy samples under a microscope to check for cancer cells. You usually have a biopsy to find out for certain if you have lung cancer. There are different ways of collecting biopsies, including:
Waiting for tests results can be a difficult time, we have more information that can help.
Further tests for lung cancer
If tests show you have lung cancer, your specialist will arrange further tests. These may be to help with the staging of lung cancer.
You may have the following tests:
Your treatment plan will depend on the stage and type of lung cancer and your general health.
A team of specialists will meet to discuss the best possible treatment for you. This is called a multidisciplinary team (MDT).
Your doctor will explain the different treatments and their side effects. They will also talk to you about the things you should consider when making treatment decisions.
You have regular follow-up appointments after treatment. This will include regular CT scans or chest x-rays
You may get anxious before the appointments. This is natural. It may help to get support from family, friends or a support organisation.
Everyone has their own way of dealing with illness and the different emotions they experience. You may find it helpful to talk things over with family and friends or your doctor or nurse.
Macmillan is also here to support you. If you would like to talk, you can:
Below is a sample of the sources used in our lung cancer information. If you would like more information about the sources we use, please contact us at email@example.com
National Institute for Health and Care Excellence (NICE). Lung cancer – Diagnosis and management. Clinical guideline 2019.
Metastatic non-small cell lung cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. 2018.
European Society for Medical Oncology (ESMO). Early and locally advanced non-small-cell lung cancer (NSCLC): ESMO clinical practice guidelines for diagnosis, treatment and follow-up. 2017.
This information has been written, revised and edited by Macmillan Cancer Support’s Cancer Information Development team. It has been reviewed by expert medical and health professionals and people living with cancer. It has been approved by Senior Medical Editor, Dr David Gilligan, Consultant Clinical Oncologist.
Our cancer information has been awarded the PIF TICK. Created by the Patient Information Forum, this quality mark shows we meet PIF’s 10 criteria for trustworthy health information.
The language we use
We want everyone affected by cancer to feel our information is written for them.
We try to make sure our information is as clear as possible. We use plain English, avoid jargon, explain any medical words, use illustrations to explain text, and make sure important points are highlighted clearly.
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