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Screening and Multiple Intervention on Lung Epidemics (SMILE)

Primary Purpose

Inflammation, Smoking Cessation, Diet Modification

Status
Active
Phase
Phase 2
Locations
Italy
Study Type
Interventional
Intervention
Cytisine
Acetylsalicylic acid
Diet Modification and Physical Activity Increase
early lung cancer detection
spirometry with CO test
anthropometic data collection
blood test
Sponsored by
Fondazione IRCCS Istituto Nazionale dei Tumori, Milano
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Inflammation focused on measuring Inflammation, Primary Prevention, Multiple Prevention, Lung Cancer Screening, Smoking Cessation, Diet, Physical Activity, CRP

Eligibility Criteria

55 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age between 55 and 75 years
  • High consumption of cigarettes (≥ 30 packs/year)
  • Elegibility to annual LDCT screening
  • Confidence in Internet use
  • Absence of tumors for at least 5 years
  • Signed informed consent form

Exclusion Criteria:

  • Hypersensitivity to acetylsalicylic acid, salicylates or any of the excipients (excipients: cellulose powder, corn starch, coating: copolymers of methacrylic acid, sodium lauryl sulfate, polysorbate 80, talc, triethyl citrate)
  • Chronic treatment with acetylsalicylic acid, or other anti-clotting or anti-coagulant drugs (for example: heparin, dicumarol)
  • Treatment with methotrexate
  • Existing Mastocytosis
  • History of asthma induced by the administration of salicylates or substances to similar activity, particularly non-steroidal anti-inflammatory drugs
  • Gastroduodenal ulcer
  • Hemorrhagic diathesis
  • Severe chronic pathology (eg: severe respiratory and / or renal and / or hepatic and / or cardiac insufficiency)
  • Serious psychiatric problems
  • Previous treatment with Cytisine
  • Abuse of alcohol or other substances (even previous)

Sites / Locations

  • Fondazione IRCCS Istituto Nazionale dei Tumori

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Other

Arm Label

Smoking cessation and Antinflammatory

Smoking cessation

Antinflammatory

Control Group

Arm Description

Smoking cessation through the administration of Cytisine (in standard and prolonged administration) + reduction of inflammatory status through the administration of Acetylsalicylic acid, diet modification and physical activity increase + standard treatment for early lung cancer detection (ultra low dose CT) + spirometry with CO test + anthropometic data collection + blood test

Smoking cessation through the administration of Cytisine (in standard and prolonged administration) + standard treatment for early lung cancer detection (ultra low dose CT) + spirometry with CO test + anthropometic data collection + blood test

reduction of inflammatory status through the administration of Acetylsalicylic acid, diet modification and physical activity increase + standard treatment for early lung cancer detection (ultra low dose CT) + spirometry with CO test + anthropometic data collection + blood test

standard treatment for early lung cancer detection (ultra low dose CT) + spirometry with CO test + anthropometic data collection + blood test

Outcomes

Primary Outcome Measures

Change in chronic inflammatory status
Reduction in the percentage of subjects with CRP>=2 mg/L

Secondary Outcome Measures

Change in smoking status
Reduction in the percentage of smokers
Change in dietary habits
Dietary intakes are collected by a self reported food frequencies questionnaire and data are expressed as the average daily/weekly consumption of foods and food groups. Servings size is defined as "natural unit" (e.g. 1 glass of soft drinks, 1 teaspoon of sugar) or as an average serving (e.g. 80 g of pasta or rice, 30 g of dried fruits). The frequency of serving size is reported as continuous measure. Data will be collected as continuous measures and will be analyzed by performing statistical models to investigate a potential relationship among changes in dietary habits and anthropometric parameters (BMI, waist circumference..), socio-demographic characteristics (gender, smoking status, physical activity), biochemical parameters (CRP blood levels), drugs assumption and the risk of chronic diseases, such as lung cancer.
Change in the physical activity
Increase in the physical activity measured by the validate short form IPAQ questionnaire (International Physical Activity Questionnaire) The items in the short IPAQ form were structured to provide separate scores on walking, moderate-intensity and vigorous-intensity activity. Computation of the total score requires summation of the duration (in minutes) and frequency (days) of each activity. METs are multiples of the resting metabolic rate and a MET-minute is computed by multiplying the MET score of an activity by the minutes performed: Walking MET-minutes/week = 3.3 * walking minutes * walking days Moderate MET-minutes/week = 4.0 * moderate-intensity activity minutes * moderate days Vigorous MET-minutes/week = 8.0 * vigorous-intensity activity minutes * vigorous-intensity days Total physical activity MET-minutes/week = sum of Walking + Moderate + Vigorous MET-minutes/week scores
Change in body mass index (BMI)
Weight and height will be combined to report BMI in kg/m^2. Reduction in BMI
Change in waist circumference
Reduction in waist circumference expressed in centimeters
Change in metabolic profile
Enhancement in blood glucose, total cholesterol, LDL, HDL and triglycerides
Change in lung cancer incidence
Reduction in lung cancer incidence
Change in lung cancer specific and overall mortality
Reduction in lung cancer specific and overall mortality

Full Information

First Posted
August 14, 2018
Last Updated
February 27, 2023
Sponsor
Fondazione IRCCS Istituto Nazionale dei Tumori, Milano
Collaborators
Istituto Di Ricerche Farmacologiche Mario Negri
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1. Study Identification

Unique Protocol Identification Number
NCT03654105
Brief Title
Screening and Multiple Intervention on Lung Epidemics
Acronym
SMILE
Official Title
Multifactorial Intervention of Primary Prevention in High Risk Subjects: a Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 23, 2019 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fondazione IRCCS Istituto Nazionale dei Tumori, Milano
Collaborators
Istituto Di Ricerche Farmacologiche Mario Negri

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This prospective randomized pilot trial will evaluate a multiple intervention program of prevention in lifelong smokers aiming at reduction of chronic inflammation status through treatment with low-dose acetylsalicylic acid (ASA), smoking cessation with cytisine, targeted modification of diet and physical activity, in addition to early diagnosis with annual ultra low-dose spiral computed tomography (LDCT).
Detailed Description
The most recent population-based studies carried out in Europe and the US on hundreds of thousands of individuals have unequivocally identified three principal causes of mortality, morbidity and chronic disability: tobacco smoke, inadequate diet, and reduced physical activity. These risk factors are in large part reversible, because in heavy smokers, even after 60 years of age, cessation is associated with a clear reduction in all-cause mortality. The finding that lifestyle and eating habits are associated with the development of cancer has been confirmed in many studies: smoking, a sedentary lifestyle, excess red meat, processed foods and sugars are associated with increased risk, while an active lifestyle, non-exposure to smoke (both active and passive), consumption of whole grains, legumes and vegetables are associated with protection or a reduced incidence in at-risk subjects. What is clear, and confirmed by many studies, is that cancer occurs more often in overweight individuals, and that cancer patients who are overweight have more difficulty treating their disease. Elevated plasma levels of C-reactive protein (CRP), even when still within normal limits, are the reflection of a chronic state of inflammation and are associated with poor prognosis in several tobacco-related diseases. CRP measurement is besides a simple test to predict the risk of heart attack and stroke as well as mortality from all causes and from cardiovascular disease. In a systematic review on adult solid tumors, elevated CRP levels were associated with higher mortality and recurrence rates, and this observation was confirmed in early-stage lung cancer by a recent meta-analysis. In patients with chronic obstructive pulmonary disease (COPD), high CRP is a strong and independent predictor of future morbidity and mortality, and an increase in CRP concurrent with a reduction of the forced expiratory volume in 1 second (FEV1) shows an even stronger effect on patient's outcome. High levels of CRP are associated with poor prognosis in cancers of the upper aerodigestive tract, rhinopharynx, lung and urinary tract. From a dietary point of view, consumption of saturated fats has been directly associated with an increase in inflammatory status as measured by high levels of CRP, just like consumption of meat, while an inverse correlation with consumption of vegetables has been observed. For example, low levels of inflammatory factors have been found in individuals adhering to a Mediterranean diet. Another recurrent finding, at least for cancer, is the importance of daily physical activity, such as brisk walking for 30 minutes. Moreover, regular physical activity is associated with better prognosis and increased survival in patients with a cancer diagnosis. The number of heavy smokers that will participate in early-diagnosis programs using spiral CT will undoubtedly increase in the future as a result of awareness campaigns, and the participating volunteers represent an excellent opportunity to evaluate the efficacy of targeted primary prevention programs. The present program will combine several interventions according to the randomization arm, proposed in combination or in single treatment, including treatment with cytisine, reduction of chronic inflammation by treatment with low-dose aspirin (ASA), targeted modification of diet and physical activity, in addition to early diagnosis with annual ultra low-dose spiral computed tomography (LDCT). At baseline each volunteer will undergo: questionnaires on population evaluation (e.g. socio-demographic, smoking habits, physical activity, etc) blood sampling for the assessment of the inflammatory and metabolic profile evaluation of respiratory function and measurement of carbon monoxide (CO) thorax ultra low-dose computed tomography (LDCT) without contrast anthropometric evaluation (e.g. weight, height, BMI, etc) To reduce levels of chronic inflammation will be used: treatment with low-dose acetylsalicylic acid (ASA) dietary / nutritional intervention in order to promote an optimal diet, based on characteristic of the Mediterranean Diet, for weight maintenance, visceral fat control and an adequate nutritional status physical activity intervention, through the reduction of sedentary behaviour and the implementation of a moderate intensity activity of about 30 min a day In the Smoking cessation will be used Cytisine. It is a molecule known since the early 60s for the treatment of smoking. In recent clinical trials it revealed efficacy in smoking cessation. In 2014, the NHS (National Health Service) produced a document evaluating the cost-effectiveness of drug treatment of smoking, concluding that cytisine has the most favorable profile among the drugs taken into consideration The imaging will be performed by volumetric acquisition with a computed tomography scanner equipped with advanced technology hardware and software, including: high performance X-ray tube with low potential, high sensitivity detectors combined with dedicated reconstruction algorithms for optimisation of the signal to noise ratio within an ultra low radiation dose. The protocol for ultra-low dose computed tomography will be specifically set for lung cancer screening with semiautomated image analysis and nodule quantification, according to the international standard for image quality (Quantitative Imaging Biomarker Alliance). In particular, the ultra-low dose computed tomography protocol will be developed for the lowest radiation exposure and tested by dedicated phantom for quantitative analysis of imaging metrics. In the control group subjects will receive an information booklet containing advice on an optimal lifestyle with particular reference to smoking, diet and physical activity according to the best international guidelines.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammation, Smoking Cessation, Diet Modification, Physical Activity, Lung Cancer
Keywords
Inflammation, Primary Prevention, Multiple Prevention, Lung Cancer Screening, Smoking Cessation, Diet, Physical Activity, CRP

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Smoking cessation and Antinflammatory
Arm Type
Experimental
Arm Description
Smoking cessation through the administration of Cytisine (in standard and prolonged administration) + reduction of inflammatory status through the administration of Acetylsalicylic acid, diet modification and physical activity increase + standard treatment for early lung cancer detection (ultra low dose CT) + spirometry with CO test + anthropometic data collection + blood test
Arm Title
Smoking cessation
Arm Type
Experimental
Arm Description
Smoking cessation through the administration of Cytisine (in standard and prolonged administration) + standard treatment for early lung cancer detection (ultra low dose CT) + spirometry with CO test + anthropometic data collection + blood test
Arm Title
Antinflammatory
Arm Type
Experimental
Arm Description
reduction of inflammatory status through the administration of Acetylsalicylic acid, diet modification and physical activity increase + standard treatment for early lung cancer detection (ultra low dose CT) + spirometry with CO test + anthropometic data collection + blood test
Arm Title
Control Group
Arm Type
Other
Arm Description
standard treatment for early lung cancer detection (ultra low dose CT) + spirometry with CO test + anthropometic data collection + blood test
Intervention Type
Drug
Intervention Name(s)
Cytisine
Other Intervention Name(s)
ev code SUB31171
Intervention Description
Cytisine administration will be randomized 1:1 in standard (40 days)and prolonged treatment (84 days). Subjects will be educated on how to take the product and informed about possible adverse effects.
Intervention Type
Drug
Intervention Name(s)
Acetylsalicylic acid
Other Intervention Name(s)
Cardioaspirin
Intervention Description
The treatment will consist of Acetylsalicylic acid at 100mg once a day
Intervention Type
Other
Intervention Name(s)
Diet Modification and Physical Activity Increase
Intervention Description
It will be proposed: an optimal diet with the aim of favoring control of weight, abdominal fat and adequate nutritional status without increasing the levels of IGF-I and inflammatory factors or glycemic peaks, with periodic verification of the results a regular and sustainable physical activity program with periodic verification of the results.
Intervention Type
Diagnostic Test
Intervention Name(s)
early lung cancer detection
Intervention Description
standard treatment for early lung cancer detection with ultra low dose CT
Intervention Type
Diagnostic Test
Intervention Name(s)
spirometry with CO test
Intervention Description
spirometry with CO test
Intervention Type
Other
Intervention Name(s)
anthropometic data collection
Intervention Description
anthropometic data collection
Intervention Type
Other
Intervention Name(s)
blood test
Intervention Description
blood test to assess the metabolic and inflammatory profile
Primary Outcome Measure Information:
Title
Change in chronic inflammatory status
Description
Reduction in the percentage of subjects with CRP>=2 mg/L
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Change in smoking status
Description
Reduction in the percentage of smokers
Time Frame
1 year
Title
Change in dietary habits
Description
Dietary intakes are collected by a self reported food frequencies questionnaire and data are expressed as the average daily/weekly consumption of foods and food groups. Servings size is defined as "natural unit" (e.g. 1 glass of soft drinks, 1 teaspoon of sugar) or as an average serving (e.g. 80 g of pasta or rice, 30 g of dried fruits). The frequency of serving size is reported as continuous measure. Data will be collected as continuous measures and will be analyzed by performing statistical models to investigate a potential relationship among changes in dietary habits and anthropometric parameters (BMI, waist circumference..), socio-demographic characteristics (gender, smoking status, physical activity), biochemical parameters (CRP blood levels), drugs assumption and the risk of chronic diseases, such as lung cancer.
Time Frame
1 year
Title
Change in the physical activity
Description
Increase in the physical activity measured by the validate short form IPAQ questionnaire (International Physical Activity Questionnaire) The items in the short IPAQ form were structured to provide separate scores on walking, moderate-intensity and vigorous-intensity activity. Computation of the total score requires summation of the duration (in minutes) and frequency (days) of each activity. METs are multiples of the resting metabolic rate and a MET-minute is computed by multiplying the MET score of an activity by the minutes performed: Walking MET-minutes/week = 3.3 * walking minutes * walking days Moderate MET-minutes/week = 4.0 * moderate-intensity activity minutes * moderate days Vigorous MET-minutes/week = 8.0 * vigorous-intensity activity minutes * vigorous-intensity days Total physical activity MET-minutes/week = sum of Walking + Moderate + Vigorous MET-minutes/week scores
Time Frame
1 year
Title
Change in body mass index (BMI)
Description
Weight and height will be combined to report BMI in kg/m^2. Reduction in BMI
Time Frame
1 year
Title
Change in waist circumference
Description
Reduction in waist circumference expressed in centimeters
Time Frame
1 year
Title
Change in metabolic profile
Description
Enhancement in blood glucose, total cholesterol, LDL, HDL and triglycerides
Time Frame
1 year
Title
Change in lung cancer incidence
Description
Reduction in lung cancer incidence
Time Frame
3 years
Title
Change in lung cancer specific and overall mortality
Description
Reduction in lung cancer specific and overall mortality
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age between 55 and 75 years High consumption of cigarettes (≥ 30 packs/year) Elegibility to annual LDCT screening Confidence in Internet use Absence of tumors for at least 5 years Signed informed consent form Exclusion Criteria: Hypersensitivity to acetylsalicylic acid, salicylates or any of the excipients (excipients: cellulose powder, corn starch, coating: copolymers of methacrylic acid, sodium lauryl sulfate, polysorbate 80, talc, triethyl citrate) Chronic treatment with acetylsalicylic acid, or other anti-clotting or anti-coagulant drugs (for example: heparin, dicumarol) Treatment with methotrexate Existing Mastocytosis History of asthma induced by the administration of salicylates or substances to similar activity, particularly non-steroidal anti-inflammatory drugs Gastroduodenal ulcer Hemorrhagic diathesis Severe chronic pathology (eg: severe respiratory and / or renal and / or hepatic and / or cardiac insufficiency) Serious psychiatric problems Previous treatment with Cytisine Abuse of alcohol or other substances (even previous)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ugo Pastorino, MD
Organizational Affiliation
IRCCS IstitutoNazionale dei Tumori di Milano
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fondazione IRCCS Istituto Nazionale dei Tumori
City
Milan
ZIP/Postal Code
20133
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
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Screening and Multiple Intervention on Lung Epidemics

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