Definitions of disease: Should possible and probable idiopathic pulmonary fibrosis be enrolled in treatment trials?

Respiratory Investigation

Volumn 53, Issue 3, 2015, Pages 88-92

  Huie, Tristan J ^a   Brown, Kevin K ^a  

^a DEPARTMENT OF MEDICINE   (United States)

Author keywords

Clinical trials; High resolution computerized tomography; Idiopathic pulmonary fibrosis; Interstitial lung disease; Pathology

Indexed keywords

CHEST IMAGING; CLINICAL FEATURE; DIAGNOSTIC IMAGING; DISEASE CLASSIFICATION; DISEASE COURSE; FIBROSING ALVEOLITIS; HISTOPATHOLOGY; HUMAN; IMAGE ANALYSIS; IMAGING; PATIENT SELECTION; POSSIBLE IDIOPATHIC PULMONARY FIBROSIS; PROBABLE IDIOPATHIC PULMONARY FIBROSIS; REVIEW; ANAMNESIS; CLINICAL TRIAL (TOPIC); COMPUTER ASSISTED TOMOGRAPHY; IDIOPATHIC PULMONARY FIBROSIS; IMAGE ENHANCEMENT; PATHOLOGY; THORAX RADIOGRAPHY;

CLINICAL TRIALS AS TOPIC; HUMANS; IDIOPATHIC PULMONARY FIBROSIS; MEDICAL HISTORY TAKING; RADIOGRAPHIC IMAGE ENHANCEMENT; RADIOGRAPHY, THORACIC; TOMOGRAPHY, X-RAY COMPUTED;

EID: 84928770758     PISSN: 22125345     EISSN: 22125353     Source Type: Journal    
DOI: 10.1016/j.resinv.2014.12.005     Document Type: Review

References (17)

1. Bjoraker J.A., Ryu J.H., Edwin M.K., et al. Prognostic significance of histopathologic subsets in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 1998, 157:199-203.
2. Raghu G., Collard H.R., Egan J.J., et al. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med 2011, 183:788-824.
3. Hunninghake G.W., Zimmerman M.B., Schwartz D.A., et al. Utility of a lung biopsy for the diagnosis of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2001, 164:193-196.
4. Lynch D.A., Godwin J.D., Safrin S., et al. High-resolution computed tomography in idiopathic pulmonary fibrosis: diagnosis and prognosis. Am J Respir Crit Care Med 2005, 172:488-493.
5. Raghu G., Mageto Y.N., Lockhart D., et al. The accuracy of the clinical diagnosis of new-onset idiopathic pulmonary fibrosis and other interstitial lung disease: a prospective study. Chest 1999, 116:1168-1174.
6. Flaherty K.R., Thwaite E., Kazerooni E.A., et al. Radiological versus histological diagnosis in UIP and NSIP: survival implications. Thorax 2003, 58:143-148.
7. Sumikawa H., Johkoh T., Colby T.V., et al. Computed tomography findings in pathological usual interstitial pneumonia: relationship to survival. Am J Respir Crit Care Med 2008, 177:433-439.
8. Gruden J.F., Panse P.M., Leslie K.O., et al. UIP diagnosed at surgical lung biopsy, 2000-2009: HRCT patterns and proposed classification system. Am J Roentgenol 2013, 200:W458-W467.
9. Raghu G., Lynch D., Godwin J.D., et al. Diagnosis of idiopathic pulmonary fibrosis with high-resolution CT in patients with little or no radiological evidence of honeycombing: secondary analysis of a randomised, controlled trial. Lancet Respir Med 2014, 2:277-284.
10. Fell C.D., Martinez F.J., Liu L.X., et al. Clinical predictors of a diagnosis of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2010, 181:832-837.
11. Shin K.E., Chung M.J., Jung M.P., et al. Quantitative computed tomographic indexes in diffuse interstitial lung disease: correlation with physiologic tests and computed tomography visual scores. J Comput Assist Tomogr 2011, 35:266-271.
12. Hansell D.M., Bankier A.A., MacMahon H., et al. Fleischner Society: glossary of terms for thoracic imaging. Radiology 2008, 246:697-722.
13. Watadani T., Sakai F., Johkoh T., et al. Interobserver variability in the CT assessment of honeycombing in the lungs. Radiology 2013, 266:936-944.
14. Martinez F.J., Safrin S., Weycker D., et al. The clinical course of patients with idiopathic pulmonary fibrosis. Ann Intern Med 2005, 142:963-967.
15. Collard H.R., King T.E., Bartelson B.B., et al. Changes in clinical and physiologic variables predict survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2003, 168:538-542.
16. Flaherty K.R., Mumford J.A., Murray S., et al. Prognostic implications of physiologic and radiographic changes in idiopathic interstitial pneumonia. Am J Respir Crit Care Med 2003, 168:543-548.
17. Jegal Y., Kim D.S., Shim T.S., et al. Physiology is a stronger predictor of survival than pathology in fibrotic interstitial pneumonia. Am J Respir Crit Care Med 2005, 171:639-644.