Lung Cancer ScreeningNCT03853967
Lung Cancer Screening by Low Dose CT Scan in a French Department (DEP KP80)
A study testing Low dose CT scan in people with Lung Cancer Screening, run by Centre Hospitalier d'Abbeville at 1 site in France.
Trial summary
Lung cancer is the leading cause of cancer death worldwide. The aims of this study were to assess the feasibility and effectiveness of a lung cancer screening pilot program with LD CT scan in a French department (Somme). DEP KP80 was a single-arm, prospective study started in May 2016. Read more about this study
- Who is it for?
- Ages 55 to 74 yearsHealthy volunteers can take part
- Conditions the study is for
- Lung Cancer Screening
- What is being tested?
- Low dose CT scan
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1,307 participants
- Where
- 1 siteFrance
- Study dates
- 15 May 2016to 15 May 2021
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 55 to 74 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- male or female
- smokers or former smoker,
- aged between 55 and 74
- tobacco exposure of more than 30 pack-years,
- active smokers or who quitted for less than 15 years,
- obvious symptoms.
Who cannot join
- history of cancer within the last 5 years other than non melanoma skin cancer or carcinoma in situ,
- worsening of their health state with Eastern Cooperative Oncology Group performance status>3,-
- heart or respiratory severe co-morbidity with contraindications to thoracoscopy
Trial locations and contacts
1 site in 1 country.
France1 site, 1 recruiting
- Recruiting
LELEU
Abbeville, Somme, 80100
olivier LELEU, 0033322255342, leleu.olivier@ch-abbeville.fr
About this study
Lung cancer is the leading cause of cancer death worldwide. The aims of this study were to assess the feasibility and effectiveness of a lung cancer screening pilot program with LD CT scan in a French department (Somme).
DEP KP80 was a single-arm, prospective study started in May 2016. The inclusion criteria were those of the National Lung Screening Trial. An annual LD CT scan was scheduled and 2 rounds were planned. Smoking cessation was encouraged as part of the protocol.
Subjects were selected by General Practitioner or Pneumologist who checked the inclusion criteria and prescribed the CT scan.
Read the detailed description
Scientific context :
Lung cancer is the deadliest cancer in France and in the world. With around 39500 new cases in 2012 in France, lung cancer ranks fourth regarding cancer incidence for both women and men. In 2012 it caused the highest number of annual deaths linked to cancer (around 30 000 deaths) according to the Institut National Du Cancer (INCA). It is a real public health issue, its incidence has been increasing above all in women and its prognosis is grim. The 1-year survival rate is 43% and 5-year survival rate 14% whatever the stage of the disease.
The Picardy region presents an excess mortality of 18% compared to the national average for the lung cancer and Somme has one of the highest incidence rate in France for this cancer.
Research hypothesis:
If the investigators know that tobacco smoke is the main risk factor, the other feature of this cancer is characterized by a diagnosis at an advanced stage when only limited, palliative treatments which are heavy, and costly can be provided Proposing the screening test with low dose helical computed tomography (LD-CT) has the aim to spot this cancer at an early stage when a curative surgical treatment is still possible in order to improve the survival chances.
Indeed screening by low dose CT showed a decrease of the death rate by 20 % of lung cancer and by 6 % for all the causes in the National Lung Screening Trial published in 2011.
If this screening test has for goal to diagnose lung cancers at an early stage, it also highlights in a quarter of the cases benign abnormalities requiring mainly further non invasive explorations. This low specificity is one of the reasons why in France the Haute Autorite Sante (HAS) has concluded that the current conditions were not met to authorize this screening in general population and insist on carrying the research for this screening.
Decreasing the number of false positives by selecting the targeted population and optimizing the decision algorithms would enable to improve the specificity of low dose CT as screening test of lung cancer.
Description of the intervention:
The rationale of this project is to use already existing networks among health care providers and between the health care providers and the departmental cancer screening agency (ADEMA 80) which is already in charge with the breast and colon cancer screening.
The targeted population of this screening concerns men and women from 55 to 74 year old who are smoking with a tobacco exposure of more than 30 pack-years or those who stopped for less than 15 years without obvious symptoms and who accept the screening tests with information on the results and the consequences which can arise ( non invasive exploration , CT after 3 months, Positon Emission Tomography scan or invasive exploration : CT guided biopsy, bronchoscopy, surgical exploration ) and who signed a consent form.
People with a history of cancer of less than 5 years, worsening of their health state, heart or respiratory morbidities which prevent a chest surgery are excluded of this study.
The population which is likely to undergo this test (male and female smokers from 55 to 74 years old) is estimated to 48 000 inhabitants for the department of the Somme which has a total population of 584 000 inhabitants.
The screening test is offered by primary care doctors and pneumologists of the Somme whom an invitation was sent by mail and who have accepted the way and means of the study.
The CT is prescribed on a prescription pad with 3 carbonless documents delivered by ADEMA 80 to the participating doctors: a part for the patient in order to take an appointment for his exam, one part which is sent back to ADEMA 80 with a prepaid envelope to keep a track and one part for the prescribing doctor. The LD-CT is carried out in radiology centers which comply with the charter of good practice of LD-CT.
The General Practitioners (GPs) and the pneumologists deal with the management of abnormalities which are eventually found by the CT according to the decision algorithms defined by the steering committee which has also validated a standard CT report. If the LD-CT proves to be normal, the screening is negative, the patient is invited again by ADEMA 80 the following year for a new LD-CT.
If the CT is abnormal , depending on the nodule' s size and/or nature either a new LD-CT is carried out after 3 months or if the screening is positive the patient's case is presented during a multidisciplinary team meeting with pneumologists, radiologists, oncologists, thoracic surgeons, pathologists.
Participants of the screening are being made aware of the benefits of quitting smoking and refer to a consultation on tobacco control if necessary.
A copy of the CT results is given to the local cancer screening agency (ADEMA 80) which is in charge with keeping a track and with statistic analyses.
This is a study with 2-year inclusion period. The length of the study is of 3 years.
It is the first study of lung cancer screening by LD-CT which is made at a regional scale in France.
Expected public health impact. The main objective of this screening is to assess the feasibility of an organized individual screening by LD-CT for a heavy smoker population aged from 55 to 74 in the Somme department, department with high incidence of lung cancer.
The secondary goals are to determine incidence of false positives, the number of screened cancers and staging, the histological subtypes, the sensibility and the specificity of this screening, to assess the treatments which have been implemented and the time it takes to deliver appropriate, to rate the quality of life and assess the incentive means to quit smoking
- Conditions
- Lung Cancer Screening
- Being tested
- Low dose CT scan
- Keywords
- low dose CT scan
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Low dose CT scanOther
low dose CT scan
| Study group | Role | What they receive |
|---|---|---|
| screening | Experimental | participants performed lung cancer screening by Low Dose CT scan Receives: Other: Low dose CT scan |
What is being measured
The primary outcome is the main question the study is designed to answer.
feasibility of lung cancer screening implementation in France: participation rate
number of participants, participation rate : number of LD CT scan performed/ number of participants
Measured: 3 years
efficacity of lung cancer screening in France: number of lung cancer diagnosed, number of stage I, rate of surgery, rate of false positive
number of lung cancer diagnosed, number of stage I, rate of surgery, rate of false positive
Measured: 3 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Feb 2019
- Study start15 May 2016
- Primary completion15 May 2020 (estimated)
- Study completion15 May 2021 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Lung Cancer ScreeningStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Screening
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- prospective single arm study
- Masking
- None (open label)
- Enrolment
- 1,307 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Centre Hospitalier d'Abbeville
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Olivier LELEU, Centre Hospitalier d'Abbeville
- Investigators
- olivier LELEU, Principal investigator, MD
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03853967
- Sponsor's protocol ID
- 160048-B81
- Status last verified
- Feb 2019
- First submitted
- 22 Feb 2019
- Last updated
- 26 Feb 2019
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 26 Feb 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Lung Cancer Screening by Low Dose CT Scan in a French Department (DEP KP80)
- ClinicalTrials.gov ID
- NCT03853967
- Acronym / sponsor ID
- 160048-B81
- Conditions
- Lung Cancer Screening
- Keywords
- low dose CT scan
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 1,307 participants (estimated)
- Lead sponsor
- Centre Hospitalier d'AbbevilleUniversity, hospital or other
- Study start
- 15 May 2016 (actual)
- Primary completion
- 15 May 2020 (estimated)
- Study completion
- 15 May 2021 (estimated)
- First posted
- 26 Feb 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Lung cancer is the leading cause of cancer death worldwide. The aims of this study were to assess the feasibility and effectiveness of a lung cancer screening pilot program with LD CT scan in a French department (Somme).
DEP KP80 was a single-arm, prospective study started in May 2016. The inclusion criteria were those of the National Lung Screening Trial. An annual LD CT scan was scheduled and 2 rounds were planned. Smoking cessation was encouraged as part of the protocol.
Subjects were selected by General Practitioner or Pneumologist who checked the inclusion criteria and prescribed the CT scan.
Detailed description
Scientific context :
Lung cancer is the deadliest cancer in France and in the world. With around 39500 new cases in 2012 in France, lung cancer ranks fourth regarding cancer incidence for both women and men. In 2012 it caused the highest number of annual deaths linked to cancer (around 30 000 deaths) according to the Institut National Du Cancer (INCA). It is a real public health issue, its incidence has been increasing above all in women and its prognosis is grim. The 1-year survival rate is 43% and 5-year survival rate 14% whatever the stage of the disease.
The Picardy region presents an excess mortality of 18% compared to the national average for the lung cancer and Somme has one of the highest incidence rate in France for this cancer.
Research hypothesis:
If the investigators know that tobacco smoke is the main risk factor, the other feature of this cancer is characterized by a diagnosis at an advanced stage when only limited, palliative treatments which are heavy, and costly can be provided Proposing the screening test with low dose helical computed tomography (LD-CT) has the aim to spot this cancer at an early stage when a curative surgical treatment is still possible in order to improve the survival chances.
Indeed screening by low dose CT showed a decrease of the death rate by 20 % of lung cancer and by 6 % for all the causes in the National Lung Screening Trial published in 2011.
If this screening test has for goal to diagnose lung cancers at an early stage, it also highlights in a quarter of the cases benign abnormalities requiring mainly further non invasive explorations. This low specificity is one of the reasons why in France the Haute Autorite Sante (HAS) has concluded that the current conditions were not met to authorize this screening in general population and insist on carrying the research for this screening.
Decreasing the number of false positives by selecting the targeted population and optimizing the decision algorithms would enable to improve the specificity of low dose CT as screening test of lung cancer.
Description of the intervention:
The rationale of this project is to use already existing networks among health care providers and between the health care providers and the departmental cancer screening agency (ADEMA 80) which is already in charge with the breast and colon cancer screening.
The targeted population of this screening concerns men and women from 55 to 74 year old who are smoking with a tobacco exposure of more than 30 pack-years or those who stopped for less than 15 years without obvious symptoms and who accept the screening tests with information on the results and the consequences which can arise ( non invasive exploration , CT after 3 months, Positon Emission Tomography scan or invasive exploration : CT guided biopsy, bronchoscopy, surgical exploration ) and who signed a consent form.
People with a history of cancer of less than 5 years, worsening of their health state, heart or respiratory morbidities which prevent a chest surgery are excluded of this study.
The population which is likely to undergo this test (male and female smokers from 55 to 74 years old) is estimated to 48 000 inhabitants for the department of the Somme which has a total population of 584 000 inhabitants.
The screening test is offered by primary care doctors and pneumologists of the Somme whom an invitation was sent by mail and who have accepted the way and means of the study.
The CT is prescribed on a prescription pad with 3 carbonless documents delivered by ADEMA 80 to the participating doctors: a part for the patient in order to take an appointment for his exam, one part which is sent back to ADEMA 80 with a prepaid envelope to keep a track and one part for the prescribing doctor. The LD-CT is carried out in radiology centers which comply with the charter of good practice of LD-CT.
The General Practitioners (GPs) and the pneumologists deal with the management of abnormalities which are eventually found by the CT according to the decision algorithms defined by the steering committee which has also validated a standard CT report. If the LD-CT proves to be normal, the screening is negative, the patient is invited again by ADEMA 80 the following year for a new LD-CT.
If the CT is abnormal , depending on the nodule' s size and/or nature either a new LD-CT is carried out after 3 months or if the screening is positive the patient's case is presented during a multidisciplinary team meeting with pneumologists, radiologists, oncologists, thoracic surgeons, pathologists.
Participants of the screening are being made aware of the benefits of quitting smoking and refer to a consultation on tobacco control if necessary.
A copy of the CT results is given to the local cancer screening agency (ADEMA 80) which is in charge with keeping a track and with statistic analyses.
This is a study with 2-year inclusion period. The length of the study is of 3 years.
It is the first study of lung cancer screening by LD-CT which is made at a regional scale in France.
Expected public health impact. The main objective of this screening is to assess the feasibility of an organized individual screening by LD-CT for a heavy smoker population aged from 55 to 74 in the Somme department, department with high incidence of lung cancer.
The secondary goals are to determine incidence of false positives, the number of screened cancers and staging, the histological subtypes, the sensibility and the specificity of this screening, to assess the treatments which have been implemented and the time it takes to deliver appropriate, to rate the quality of life and assess the incentive means to quit smoking
Study design
- Primary purpose
- Screening
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- prospective single arm study
| Arm | Type | Receives |
|---|---|---|
| screening | Experimental | Other: Low dose CT scanparticipants performed lung cancer screening by Low Dose CT scan |
Who may qualify
- Ages
- 55 to 74 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- male or female
- smokers or former smoker,
- aged between 55 and 74
- tobacco exposure of more than 30 pack-years,
- active smokers or who quitted for less than 15 years,
Key exclusion criteria (3 listed)
- history of cancer within the last 5 years other than non melanoma skin cancer or carcinoma in situ,
- worsening of their health state with Eastern Cooperative Oncology Group performance status>3,-
- heart or respiratory severe co-morbidity with contraindications to thoracoscopy
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Low dose CT scanlow dose CT scan | Other | screening |
Primary outcome
feasibility of lung cancer screening implementation in France: participation rate
Time frame: 3 years
number of participants, participation rate : number of LD CT scan performed/ number of participants
efficacity of lung cancer screening in France: number of lung cancer diagnosed, number of stage I, rate of surgery, rate of false positive
Time frame: 3 years
number of lung cancer diagnosed, number of stage I, rate of surgery, rate of false positive
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Feb 2019.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
olivier LELEU principal investigator
MD
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Low dose CT scan in people with Lung Cancer Screening, run by Centre Hospitalier d'Abbeville at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 26 Feb 2019. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact olivier LELEU (0033322255342, leleu.olivier@ch-abbeville.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
feasibility of lung cancer screening implementation in France: participation rate (time frame: 3 years). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Feb 2019.