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Studies Examining the Importance of Smoking After Being Diagnosed With Lung Cancer

Does Smoking Status After Being Diagnosed With Lung Cancer Influence Outcome? An Observational Cohort Study.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01192256
Acronym
LungCast
Enrollment
2400
Registered
2010-09-01
Start date
2010-03-31
Completion date
2021-03-15
Last updated
2022-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Keywords

smoking, cessation, mortality, quality of life

Brief summary

A large project consisting of: a) an observational trial where smoking status is recorded on 1400 consecutive people newly diagnosed with lung cancer. Smoking status is biologically validated with exhaled carbon monoxide (eCO) levels every 3 months. Survival, cancer progression and treatment complications will be recorded and compared in smokers, ex-smokers and never smokers.

Detailed description

Smoking causes around 85% of lung cancer. Continued smoking after diagnosis probably worsens survival and increases treatment complications but prospective well-designed studies are lacking. This project is an observational cohort study recording outcomes in smokers, never-smokers, and ex-smokers, using exhaled carbon monoxide to validate smoking status when they attend for further lung cancer clinics. This project is unique, as every patient with a clinical diagnosis of lung cancer will have their smoking status biologically validated by a quick and easy test, and those enrolled in the smoking cessation treatments or not will also complete a generic quality of life questionnaire at regular intervals. These appointments will coincide with other hospital appointments wherever possible, and survival status will reported up to 24 months after enrolment.

Interventions

None listed

Sponsors

Cardiff and Vale University Health Board
CollaboratorOTHER_GOV
Dr Keir Lewis
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* clinical diagnosis of lung cancer

Exclusion criteria

* refusal Consent * inability to provide exhaled CO * active psychiatric illness or substance misuse * concurrent malignancies of another type other than non-melanoma skin cancer * unable to travel for sessions with smoking cessation counsellor and / or outpatient visits from outset * WHO performance status 4 * Life expectancy less than 6 weeks.

Design outcomes

Primary

MeasureTime frame
Median and 2-year survival rates in confirmed smokers versus non- smokers newly diagnosed with lung cancer.24 months

Secondary

MeasureTime frame
Number of treatment complications in smokers versus non-smokers (frequency surgical wound complications, radiotherapy induced pneumonitis and median total radiation (Gy) dose; frequency and duration of neutropenic sepses2 years
Point prevalence of smoking at 0, 3, 6 12, 24 months2 years
Median survival and 2-year survival rates by smoking status for early (Stage I/II NSCLC) versus those with advanced (Stage III/IV) NSCLC.24 months
Accrual and attendance rates of lung cancer patients attending a hospital smoking cessation service2 years
Estimate of cost per quality adjusted life year gained by smoking cessation advice in both quit strategies for smokers2 years
Comparison of changes in health related quality of life (EQ5D) in smokers versus non-smokers2 years

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026