Screening for Lung Cancer in Current or Past Smokers With Chronic Obstructive Pulmonary Disease

University College London (UCL)

Status: Completed

Conditions: Precancerous Condition; Lung Cancer

Treatments: Procedure: Autofluorescence bronchoscopy; Other: Chest x ray; Other: cytology and cytometry specimen collection procedure; Procedure: CT scan

Study type: Interventional

Funder types: Other

Identifiers

NCT00512746

CDR0000558413

EU-20738

ISRCTN80745975

CRUK-BRD/06/10

Details and patient eligibility

About

RATIONALE: Screening tests or exams may help doctors find lung cancer sooner, when it may be easier to treat.

PURPOSE: This randomized clinical trial is studying screening tests or exams to see how well they work compared to usual care in finding early stage lung cancer in current or past smokers with chronic obstructive pulmonary disease.

Full description

OBJECTIVES:

Primary

• To show that the proportion of lung cancer diagnosed at stage I or II is significantly greater in the surveillance arm than in the control arm.

Secondary

• Establish whether sputum cytology and/or cytometry can be employed to stratify patients with chronic obstructive pulmonary disease (COPD) according to their risk of developing incidence lung cancer.
• Identify patients with pre-invasive lesions in their airways and examine the risk of developing lung cancer in patients harboring these lesions.
• Provide an opportunity to archive blood samples from patients under surveillance to enable the identification of markers of disease progression.
• Examine the compliance of regular screening among patients in this high-risk group.
• Determine the proportion of patients in which it is not possible to provide a sputum screening result.

OUTLINE: This is a randomized, controlled, multicenter study. Patients are stratified according to recruiting site, age, gender, smoking history (current vs ex-smoker) and severity of chronic obstructive pulmonary disease (COPD) (mild vs moderate). Patients are randomized to 1 of 2 arms.

• Control arm: Patients are managed according to the usual practice of their hospital or general practice for their COPD treatment. They undergo no particular investigations except those that may arise due to a change in their clinical condition. Those patients who are not diagnosed with lung cancer during the course of the study are offered a chest x-ray after 5 years of follow-up.
• Surveillance arm: Patients undergo surveillance for 5 years. A sputum sample is collected for cytology and cytometry. If the sputum sample is normal the patient is asked to provide a sputum sample annually. If the sputum sample is abnormal the patient undergoes an annual spiral CT scan followed by autofluorescence bronchoscopy. At bronchoscopy, the following samples are taken: bronchial washings, bronchial brushings, and bronchial biopsies. Bronchoscopy is repeated every 4-12 months depending upon the histology results. If an invasive lesion is found, the patient is referred for treatment via the normal hospital systems. Any remaining sputum sample is stored frozen as part of the tissue bank associated with this trial.

Peer Reviewed and Funded or Endorsed by Cancer Research UK.

Enrollment: 1,569 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

Inclusion criteria:

• Meets 1 of the following criteria:

  • Current smoker, defined as ≥ a 20 pack year smoking history and/or 20 year duration of smoking
  • Ex-smoker who has quit smoking within the past 8 years AND has ≥ a 20 pack year smoking history and/or 20 year duration of smoking

• Mild to moderate chronic obstructive pulmonary disease (COPD) as defined by the GOLD criteria

  • Mild COPD: FEV_1/forced vital capacity (FVC) < 70%; FEV_1 ≥ 80% of predicted*
  • Moderate COPD: FEV_1/FVC < 70%; FEV_1 50-80% of predicted* NOTE: *Spirometric values will be obtained post bronchodilator according to the recommendations in the GOLD criteria

Exclusion criteria:

• Inadequate lung function (FEV_1 < 50% of predicted after bronchodilator)

PATIENT CHARACTERISTICS:

Inclusion criteria:

• Life expectancy must be at least 5 years

Exclusion criteria:

• History of malignant disease within the past 5 years except non-melanomatous skin cancers
• Other serious co-morbidity
• Evidence of severe or uncontrolled systemic diseases that, in the view of the investigator, makes it undesirable for the patient to participate in this trial
• Any disorder making reliable informed consent impossible
• Unlikely to co-operate with a 5 year follow-up

PRIOR CONCURRENT THERAPY:

• Patients may receive all concurrent therapy deemed to provide adequate care as decided by their medical doctors

Trial design

Primary purpose: Screening

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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1,569 participants in 2 patient groups

Surveillance

Other group

Description:

Screened arm

Treatment:

Procedure: CT scan

Other: cytology and cytometry specimen collection procedure

Procedure: Autofluorescence bronchoscopy

Other: Chest x ray

Control

Active Comparator group

Description:

Control arm

Treatment:

Other: Chest x ray