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Minimum Dose Computed Tomography of the Thorax for Follow-up in Patients With Resected Lung Carcinoma


Phase 2
18 Years
N/A
Open (Enrolling)
Both
Non-small Cell Lung Cancer

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Trial Information

Minimum Dose Computed Tomography of the Thorax for Follow-up in Patients With Resected Lung Carcinoma


Lung Carcinoma is expected to kill 18,900 men and women in Canada in 2004. This is more than
the combined total for the next three common cancers. The most important factor that
determines patient survival is the stage of disease at presentation. Surgical resection is
the best chance of cure. However, patients who undergo lung resection with curative intent
have a significant incidence of a second lung cancer at 2% per year and a recurrence rate of
38% at 5 years. The current follow-up of these patients relies on periodic physical
examination and chest radiography(CXR). However, CXR is insensitive in the detection of lung
nodules when compared to standard Computed Tomography of the thorax (SDCT). Computed
Tomography detects smaller lung nodules than CXR however, the radiation dose from a SDCT is
roughly equivalent to 20 CXR examinations. Screening studies using Low Dose CT of the Thorax
(LDCT) in subjects at high risk for lung cancer have demonstrated that LDCT detects three
times as many nodules as CXR and four times as many primary lung cancers at one-third the
dose of SDCT. Phantom and clinical work with LDCT performed at UHN/MSH suggests that a
further reduction in radiation dose (Minimum Dose CT -MnDCT) is possible for nodule
detection. Minimum dose CT is performed at a dose one sixth of a SDCT.In addition, if MnDCT
is confirmed to be a more sensitive nodule detection technique, it could be used to

1. Increase the interval between repeat out-patient assessment and thereby 2. Reduce the
overall cost of surveillance and inconvenience to the patient and 3. Free up clinic
time for the surgeon to review more patients and reduce waiting lists


Inclusion Criteria:



- lung cancer patients undergoing resection with intent to cure

Exclusion Criteria:

- age < 18 years

Type of Study:

Interventional

Study Design:

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Outcome Measure:

Detection of local recurrent disease

Outcome Time Frame:

5 years

Safety Issue:

No

Principal Investigator

Narinder Paul, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

University Health Network, Toronto

Authority:

Canada: Health Canada

Study ID:

05-0051-C

NCT ID:

NCT00188279

Start Date:

July 2005

Completion Date:

April 2017

Related Keywords:

  • Non-Small Cell Lung Cancer
  • ct
  • scan
  • lung
  • follow-up
  • Carcinoma
  • Carcinoma, Non-Small-Cell Lung
  • Lung Neoplasms

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