search
Back to results

Utility of LDCT in Lung Cancer Screening in a TB Endemic Region

Primary Purpose

Lung Cancer

Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Low-dose computed tomography of chest
Sponsored by
Postgraduate Institute of Medical Education and Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Lung Cancer focused on measuring lung cancer, ldct, low-dose CT, screening, lung nodule

Eligibility Criteria

50 Years - 74 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Individuals aged 55-74 years with at least 30 pack-year history of smoking (or smoking index ≥600) who are current smokers or quit within the last 15 years OR
  • Individuals aged 50-74 years with at least 20 pack-year history of smoking (or smoking index ≥400) who are current or former smokers with COPD or family history of lung cancer in any first-degree relative

Exclusion Criteria:

  • Symptomatic structural lung disease other than COPD (e.g. bronchiectasis, chronic pulmonary aspergillosis, pulmonary fibrosis)
  • Severe comorbid condition which is likely to limit the survival of the patient in the opinion of the investigator (e.g. advanced lung disease, cardiovascular disease, chronic kidney disease, chronic liver disease)
  • Presence of symptoms which lead to a suspicion of lung cancer (e.g. hemoptysis or unexplained weight loss [>5 kg] within the last 6 months)
  • Conditions which may interfere interpretation of CT (e.g. metallic implants on chest wall, cardiac pacemakers)
  • Treatment for any other cancer in the last 5 years
  • Pulmonary infection (for which treatment with antimicrobials is indicated) which is active at present or was recent (within the last 3 months)
  • Patients who have underwent CT chest within the last 18 months
  • Negative consent

Sites / Locations

  • Postgraduate Institute of Medical Education and Research (PGIMER)

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

LDCT arm

Arm Description

All eligible participants will undergo screening with LDCT

Outcomes

Primary Outcome Measures

Positivity rate with LDCT screening
The proportion of participants with a positive result among the total number of individuals screened with LDCT

Secondary Outcome Measures

Rate of detection of lung cancer
Rate of lung cancer detection among study participants
False positive rate
Rate of false positive results with LDCT screening
Proportion of patients requiring additional procedures (imaging/invasive procedures)
The proportion of patients with positive results on initial LDCT scan requiring additional procedures (imaging/invasive procedures)
Proportion of patients developing complications due to additional procedures
The proportion of patients among those who developed complications due to additional procedures (imaging/invasive procedures) performed after initial LDCT scan
Change in the 6-item Spielberger State-Trait Anxiety Inventory (STAI-6) questionnaire score
Change in anxiety levels from baseline after conveying LDCT results to the patient
Cost in Indian Rupees to detect one case of lung cancer by LDCT screening
Cost-effectiveness of LDCT screening
Proportion of patients who quit/re-initiated smoking after inclusion in study
The proportion of patients who quit/re-initiated smoking after inclusion in study

Full Information

First Posted
April 5, 2019
Last Updated
March 26, 2022
Sponsor
Postgraduate Institute of Medical Education and Research
search

1. Study Identification

Unique Protocol Identification Number
NCT03909620
Brief Title
Utility of LDCT in Lung Cancer Screening in a TB Endemic Region
Official Title
A Study Assessing the Utility of Low-dose Computed Tomography (LDCT) in Lung Cancer Screening in North India
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
May 1, 2019 (Actual)
Primary Completion Date
March 31, 2020 (Actual)
Study Completion Date
December 31, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Postgraduate Institute of Medical Education and Research

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Lung cancer screening with low-dose computed tomography (LDCT) has been recently shown to result in a significant reduction in lung cancer-specific mortality. However, the utility of LDCT screening in developing countries with high incidence of tuberculosis has not been adequately studied. The investigators hypothesize that LDCT screening in tuberculosis endemic regions is likely to yield a large proportion of false-positive results, especially in the initial round of screening, posing a significant burden on the healthcare system. Herein, the investigators assess the utility of LDCT and its cost-effectiveness in India.
Detailed Description
Screening for lung cancer may reduce lung cancer mortality by diagnosing the disease at an early stage when it is treatable more effectively. There are several methods available for screening of lung cancer. These include sputum cytology, chest radiography, computed tomography (CT) of the chest, and positron emission tomography (PET). However, sputum cytology and chest radiography have been found to be ineffective as screening tests for lung cancer as there is no reduction in lung cancer mortality. The use of CT or PET for lung cancer screening may be associated with unacceptable levels of radiation exposure and enormous cost. Low-dose computed tomography (LDCT) of the chest is a special type of CT, which uses relatively low radiation exposure to create a low-resolution image of the entire thorax. The radiation exposure associated with LDCT is 5-6 times less than that of a conventional CT scan of the thorax. LDCT screening has been to shown to result in a 20% reduction in lung cancer-specific mortality. Several national and international guidelines recommend this strategy for lung cancer screening. Despite these guidelines and recommendations by several organizations, lung cancer screening has not been established in several developing countries, where a controversy arises due to high rates of granulomatous diseases like tuberculosis. Emerging evidence indicates that false positive results with LDCT in developing countries may not be unacceptably high as previously believed. In this study, the investigators intend to assess the utility of lung cancer screening using low-dose computed tomography (LDCT) in India, a country with high prevalence of tuberculosis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer
Keywords
lung cancer, ldct, low-dose CT, screening, lung nodule

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
253 (Actual)

8. Arms, Groups, and Interventions

Arm Title
LDCT arm
Arm Type
Experimental
Arm Description
All eligible participants will undergo screening with LDCT
Intervention Type
Diagnostic Test
Intervention Name(s)
Low-dose computed tomography of chest
Other Intervention Name(s)
LDCT, Low-dose CT
Intervention Description
Eligible subjects will undergo a single round of LDCT screening. The LDCT will be considered as positive if a solid nodule or part-solid nodule of size ≥6 mm or non-solid nodule of size ≥20 mm is identified. Evaluation of positive nodules will be performed as per existing standard recommendations
Primary Outcome Measure Information:
Title
Positivity rate with LDCT screening
Description
The proportion of participants with a positive result among the total number of individuals screened with LDCT
Time Frame
After baseline LDCT scan results are available (an average of 1 week after LDCT scan)
Secondary Outcome Measure Information:
Title
Rate of detection of lung cancer
Description
Rate of lung cancer detection among study participants
Time Frame
Up to 6 months after the LDCT scan
Title
False positive rate
Description
Rate of false positive results with LDCT screening
Time Frame
Up to 6 months after the LDCT scan
Title
Proportion of patients requiring additional procedures (imaging/invasive procedures)
Description
The proportion of patients with positive results on initial LDCT scan requiring additional procedures (imaging/invasive procedures)
Time Frame
Up to 6 months after the LDCT scan
Title
Proportion of patients developing complications due to additional procedures
Description
The proportion of patients among those who developed complications due to additional procedures (imaging/invasive procedures) performed after initial LDCT scan
Time Frame
Up to 2 weeks after the diagnostic procedure
Title
Change in the 6-item Spielberger State-Trait Anxiety Inventory (STAI-6) questionnaire score
Description
Change in anxiety levels from baseline after conveying LDCT results to the patient
Time Frame
After communication of baseline LDCT results (an average of 1-2 weeks after the LDCT scan)
Title
Cost in Indian Rupees to detect one case of lung cancer by LDCT screening
Description
Cost-effectiveness of LDCT screening
Time Frame
Up to 6 months after the LDCT scan
Title
Proportion of patients who quit/re-initiated smoking after inclusion in study
Description
The proportion of patients who quit/re-initiated smoking after inclusion in study
Time Frame
Up to 6 months after the LDCT scan

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
74 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Individuals aged 55-74 years with at least 30 pack-year history of smoking (or smoking index ≥600) who are current smokers or quit within the last 15 years OR Individuals aged 50-74 years with at least 20 pack-year history of smoking (or smoking index ≥400) who are current or former smokers with COPD or family history of lung cancer in any first-degree relative Exclusion Criteria: Symptomatic structural lung disease other than COPD (e.g. bronchiectasis, chronic pulmonary aspergillosis, pulmonary fibrosis) Severe comorbid condition which is likely to limit the survival of the patient in the opinion of the investigator (e.g. advanced lung disease, cardiovascular disease, chronic kidney disease, chronic liver disease) Presence of symptoms which lead to a suspicion of lung cancer (e.g. hemoptysis or unexplained weight loss [>5 kg] within the last 6 months) Conditions which may interfere interpretation of CT (e.g. metallic implants on chest wall, cardiac pacemakers) Treatment for any other cancer in the last 5 years Pulmonary infection (for which treatment with antimicrobials is indicated) which is active at present or was recent (within the last 3 months) Patients who have underwent CT chest within the last 18 months Negative consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kuruswamy T Prasad, MD, DM
Organizational Affiliation
Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rajinder Basher, MD
Organizational Affiliation
Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mandeep Garg, MD
Organizational Affiliation
Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sandeep Grover, MD
Organizational Affiliation
Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Naveen Kalra, MD
Organizational Affiliation
Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Navneet Singh, MD
Organizational Affiliation
Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kathirvel Soundappan, MD
Organizational Affiliation
Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh
Official's Role
Principal Investigator
Facility Information:
Facility Name
Postgraduate Institute of Medical Education and Research (PGIMER)
City
Chandigarh
ZIP/Postal Code
160012
Country
India

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Utility of LDCT in Lung Cancer Screening in a TB Endemic Region

We'll reach out to this number within 24 hrs