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Second Primary Lung Cancer Cohort Study (SPORT)

NHS Foundation Trust logo

NHS Foundation Trust

Status

Enrolling

Conditions

Lung Cancer

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Patients who have had curative treatment for lung cancer are at an increased risk of developing second primary lung cancers (and other cancers) over the next 10 years. Doctors need to develop better ways of monitoring patients during follow up so we can intervene as quickly as possible with further treatments. Measuring DNA in the blood which has come from the tumour, so called circulating tumour DNA (ctDNA), may be one way to do this.

Full description

This is a multi-centre, observational basic science study to follow patient who have undergone radical treatment, surgery or radiotherapy for Non-small Cell Lung Cancer (NSCLC) between two and five years previously. Following consent, participants will be asked to provide blood samples every six months for up to the next five years. Information from their routine clinical care, including information from any imaging, diagnostic tissue samples and blood tests will be collected. We will also request access to any original surplus diagnostic material, as well as future, excess tissue from diagnostic samples.

Blood samples will be analysed using various new scientific techniques looking to correlate emergence of new primary cancer (or recurrence of original NSCLC) with blood based markers.

Enrollment

850 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • previous treatment with curative intent (surgery or radical (chemo)radiotherapy) for stage I-IIIA primary NSCLC
  • at least two years post first treatment date of first primary NSCLC
  • able to provide informed consent

Exclusion criteria

  • Primary lung tumour was a carcinoid tumour
  • in the opinion of the managing clinician, thought unlikely to survive 12 months from time of potential recruitment.

Trial contacts and locations

1

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Central trial contact

Sarah Fielding, PhD; Robert Rintoul, PhD FRCP

Data sourced from clinicaltrials.gov

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