Cryptogenic fibrosing alveolitis: response to corticosteroid treatment and its effect on survival
Cardiothoracic Institute, Brompton Hospital, London
We have studied retrospectively 220 patients with cryptogenic fibrosing alveolitis (CFA) who were first seen between 1955-73 and had been followed up for at least four years until 1977. Seventy-seven patients had received no treatment and 143 had received corticosteroids. The only clinical difference between the groups was the age at presentation (untreated mean age 61 years±11 SD; treated mean age 56 years±11 SD p <0·001). The influence of corticosteroid treatment has been assessed both in terms of the clinical, radiographic, and physiological response after four to eight weeks and in terms of survival, using a log rank method of analysis. Of 143 treated cases 127 had detailed follow-up information. Seventy-two (57%) had substantial subjective improvement of breathlessness but only 22 (17%) of the total showed additional objective improvement. The only factors significantly distinguishing the 72 subjective responders from the 55 non-responders, and which therefore might be used as predictors of response, were a younger age at presentation (p <0·001) and less dyspnoea (p <0·02). Analysis of survival data demonstrated that treated patients who showed an early good response to steroids had a markedly better survival than non-responders (p <0·001). The survival curve for the untreated group lay between the two steroid groups. Analysis of the survival data suggests that steroid responsiveness relates particularly to a subgroup with an inherently better prognosis, which is characterised by a younger age and probably by a cellular histology not however necessarily typical of desquamative interstitial pneumonia. Nevertheless treatment appears to have an additional influence on survival especially in early disease, which is not observed in the untreated cases. A large number of factors are not related either to steroid responsiveness or to survival and these include the presence of associated "connective tissue" diseases, autoantibodies, and the duration of dyspnoea at presentation. It is concluded that biopsy information is valuable in assessment of potential to respond to steroids and that if steroid treatment is to be helpful it must be used at an early stage. The response is very variable and titration of the steroid dose against an individual patient's response is likely to give better results than adherence to arbitrary dose schedules.
This article has been cited by other articles:
-
Kim, R., Meyer, K. C.
(2008). Review: Therapies for interstitial lung disease: past, present and future. Ther Adv Respir Dis
2: 319-338
[Abstract] -
Rogliani, P., Mura, M., Assunta Porretta, M., Saltini, C.
(2008). Review: New perspectives in the treatment of idiopathic pulmonary fibrosis. Ther Adv Respir Dis
2: 75-93
[Abstract] -
Englert, J. M., Hanford, L. E., Kaminski, N., Tobolewski, J. M., Tan, R. J., Fattman, C. L., Ramsgaard, L., Richards, T. J., Loutaev, I., Nawroth, P. P., Kasper, M., Bierhaus, A., Oury, T. D.
(2008). A Role for the Receptor for Advanced Glycation End Products in Idiopathic Pulmonary Fibrosis. Am. J. Pathol.
172: 583-591
[Abstract] [Full Text] -
Rudd, R. M, Prescott, R. J, Chalmers, J C, Johnston, I. D A, for the Fibrosing Alveolitis Subcommittee of the R,
(2007). British Thoracic Society Study on cryptogenic fibrosing alveolitis: response to treatment and survival. Thorax
62: 62-66
[Abstract] [Full Text] -
Raghu, G.
(2006). Idiopathic pulmonary fibrosis: treatment options in pursuit of evidence-based approaches.. Eur Respir J
28: 463-465
[Full Text] -
Martinez, F. J., Flaherty, K.
(2006). Pulmonary function testing in idiopathic interstitial pneumonias.. Proc Am Thorac Soc
3: 315-321
[Abstract] [Full Text] -
Walter, N., Collard, H. R., King, T. E. Jr.
(2006). Current perspectives on the treatment of idiopathic pulmonary fibrosis.. Proc Am Thorac Soc
3: 330-338
[Abstract] [Full Text] -
Kubo, H., Nakayama, K., Yanai, M., Suzuki, T., Yamaya, M., Watanabe, M., Sasaki, H.
(2005). Anticoagulant Therapy for Idiopathic Pulmonary Fibrosis. Chest
128: 1475-1482
[Abstract] [Full Text] -
Grijm, K., Verberne, H. J., Krouwels, F. H., Weller, F. R., Jansen, H. M., Bresser, P.
(2005). Semiquantitative 67Ga Scintigraphy as an Indicator of Response to and Prognosis After Corticosteroid Treatment in Idiopathic Interstitial Pneumonia. JNM
46: 1421-1426
[Abstract] [Full Text] -
Kondoh, Y., Taniguchi, H., Yokoi, T., Nishiyama, O., Ohishi, T., Kato, T., Suzuki, K., Suzuki, R.
(2005). Cyclophosphamide and low-dose prednisolone in idiopathic pulmonary fibrosis and fibrosing nonspecific interstitial pneumonia. Eur Respir J
25: 528-533
[Abstract] [Full Text] -
Swigris, J. J., Kuschner, W. G., Kelsey, J. L., Gould, M. K.
(2005). Idiopathic Pulmonary Fibrosis: Challenges and Opportunities for the Clinician and Investigator. Chest
127: 275-283
[Abstract] [Full Text] -
Collard, H. R., Ryu, J. H., Douglas, W. W., Schwarz, M. I., Curran-Everett, D., King, T. E. Jr., Brown, K. K.
(2004). Combined Corticosteroid and Cyclophosphamide Therapy Does Not Alter Survival in Idiopathic Pulmonary Fibrosis. Chest
125: 2169-2174
[Abstract] [Full Text] -
Kaminski, N., Belperio, J. A., Bitterman, P. B., Chen, L., Chensue, S. W., Choi, A. M.K., Dacic, S., Dauber, J. H., du Bois, R. M., Enghild, J. J., Fattman, C. L., Grutters, J. C., Haegens, A., Hanford, L. E., Heintz, N., Henson, P. M., Hogaboam, C., Kagan, V. E., Keane, M. P., Kunkel, S. L., Land, S., Loyd, J. E., Lukacs, N., MacPherson, M., Manning, B., Manning, N., Martinelli, M., Moller, D. R., Morse, D., Mossman, B., Noble, P. W., Nowak, N., Oury, T. D., Pardo, A., Perez, A., Petty, T. L., Phan, S. H., Ramos-Nino, M. E., Ray, P., Rogers, R. M., Sato, H., Scapoli, L., Schaefer, L. M., Selman, M., Stern, M., Strollo, D. C., Tyurin, V. A., Valnickova, Z., Welsh, K. I., Witzmann, F. A., Yousem, S. A., Strieter, R. M.
(2003). Idiopathic Pulmonary Fibrosis. Am. J. Respir. Cell Mol. Bio.
29: S1-105
[Full Text] -
Flaherty, K. R., Mumford, J. A., Murray, S., Kazerooni, E. A., Gross, B. H., Colby, T. V., Travis, W. D., Flint, A., Toews, G. B., Lynch, J. P. III, Martinez, F. J.
(2003). Prognostic Implications of Physiologic and Radiographic Changes in Idiopathic Interstitial Pneumonia. Am. J. Respir. Crit. Care Med.
168: 543-548
[Abstract] [Full Text] -
Collard, H. R., King, T. E. Jr
(2003). Demystifying Idiopathic Interstitial Pneumonia. Arch Intern Med
163: 17-29
[Abstract] [Full Text] -
Nicholson, A. G., Fulford, L. G., Colby, T. V., du Bois, R. M., Hansell, D. M., Wells, A. U.
(2002). The Relationship between Individual Histologic Features and Disease Progression in Idiopathic Pulmonary Fibrosis. Am. J. Respir. Crit. Care Med.
166: 173-177
[Abstract] [Full Text] -
Wahidi, M. M., Ravenel, J., Palmer, S. M., McAdams, H. P.
(2002). Progression of Idiopathic Pulmonary Fibrosis in Native Lungs After Single Lung Transplantation*. Chest
121: 2072-2076
[Abstract] [Full Text] -
KING, T. E. JR., TOOZE, J. A., SCHWARZ, M. I., BROWN, K. R., CHERNIACK, R. M.
(2001). Predicting Survival in Idiopathic Pulmonary Fibrosis . Scoring System and Survival Model. Am. J. Respir. Crit. Care Med.
164: 1171-1181
[Abstract] [Full Text] -
Rajasekaran, B. A., Shovlin, D., Lord, P., Kelly, C. A.
(2001). Interstitial lung disease in patients with rheumatoid arthritis: a comparison with cryptogenic fibrosing alveolitis. Rheumatology (Oxford)
40: 1022-1025
[Abstract] [Full Text] -
Gross, T. J., Hunninghake, G. W.
(2001). Idiopathic Pulmonary Fibrosis. NEJM
345: 517-525
[Full Text] -
Clark, M, Cooper, B, Singh, S, Cooper, M, Carr, A, Hubbard, R
(2001). A survey of nocturnal hypoxaemia and health related quality of life in patients with cryptogenic fibrosing alveolitis. Thorax
56: 482-486
[Abstract] [Full Text] -
NICHOLSON, A. G., COLBY, T. V., DUBOIS, R. M., HANSELL, D. M., WELLS, A. U.
(2000). The Prognostic Significance of the Histologic Pattern of Interstitial Pneumonia in Patients Presenting with the Clinical Entity of Cryptogenic Fibrosing Alveolitis. Am. J. Respir. Crit. Care Med.
162: 2213-2217
[Abstract] [Full Text] -
Bourke, S. C, Clague, H.
(2000). Review of cryptogenic fibrosing alveolitis, including current treatment guidelines. Postgrad. Med. J.
76: 618-624
[Full Text] -
Michaelson, J. E., Aguayo, S. M., Roman, J.
(2000). Idiopathic Pulmonary Fibrosis : A Practical Approach for Diagnosis and Management. Chest
118: 788-794
[Full Text] -
Hacking, D., Smyth, R., Shaw, N., Kokia, G., Carty, H., Heaf, D.
(2000). Idiopathic pulmonary fibrosis in infants: good prognosis with conservative management. Arch. Dis. Child.
83: 152-157
[Abstract] [Full Text] -
Zisman, D. A., Lynch, J. P. III, Toews, G. B., Kazerooni, E. A., Flint, A., Martinez, F. J.
(2000). Cyclophosphamide in the Treatment of Idiopathic Pulmonary Fibrosis : A Prospective Study in Patients Who Failed To Respond to Corticosteroids. Chest
117: 1619-1626
[Abstract] [Full Text] -
King, T.
(2000). Idiopathic Pulmonary Fibrosis: Diagnosis and Treatment . International Consensus Statement. Am. J. Respir. Crit. Care Med.
161: 646-664
[Full Text] -
MASON, R. J., SCHWARZ, M. I., HUNNINGHAKE, G. W., MUSSON, R. A.
(1999). Pharmacological Therapy for Idiopathic Pulmonary Fibrosis . Past, Present, and Future. Am. J. Respir. Crit. Care Med.
160: 1771-1777
[Full Text] -
DANIIL, Z. D., GILCHRIST, F. C., NICHOLSON, A. G., HANSELL, D. M., HARRIS, J., COLBY, T. V., du BOIS, R. M.
(1999). A Histologic Pattern of Nonspecific Interstitial Pneumonia Is Associated with a Better Prognosis Than Usual Interstitial Pneumonia in Patients with Cryptogenic Fibrosing Alveolitis. Am. J. Respir. Crit. Care Med.
160: 899-905
[Abstract] [Full Text] -
Mitchell, D. M, Woodcock, A.
(1999). Introduction. Thorax
54: S1-1
-
COTTIN, V., DONSBECK, A.-V., REVEL, D., LOIRE, R., CORDIER, J.-F.
(1998). Nonspecific Interstitial Pneumonia . Individualization of a Clinicopathologic Entity in a Series of 12 Patients. Am. J. Respir. Crit. Care Med.
158: 1286-1293
[Abstract] [Full Text] -
(1998). International Guidelines for the Selection of Lung Transplant Candidates. Am. J. Respir. Crit. Care Med.
158: 335-339
[Full Text] -
Mapel, D. W, Hunt, W. C, Utton, R., Baumgartner, K. B, Samet, J. M, Coultas, D. B
(1998). Idiopathic pulmonary fibrosis: survival in population based and hospital based cohorts. Thorax
53: 469-476
[Abstract] [Full Text] -
GAY, S. E., KAZEROONI, E. A., TOEWS, G. B., LYNCH, J. P. III, GROSS, B. H., CASCADE, P. N., SPIZARNY, D. L., FLINT, A., ANTHONY SCHORK, M., WHYTE, R. I., POPOVICH, J., HYZY, R., MARTINEZ, F. J.
(1998). Idiopathic Pulmonary Fibrosis . Predicting Response to Therapy and Survival. Am. J. Respir. Crit. Care Med.
157: 1063-1072
[Abstract] [Full Text] -
KATZENSTEIN, A.-L. A., MYERS, J. L.
(1998). Idiopathic Pulmonary Fibrosis . Clinical Relevance of Pathologic Classification. Am. J. Respir. Crit. Care Med.
157: 1301-1315
[Full Text] -
BJORAKER, J. A., RYU, J. H., EDWIN, M. K., MYERS, J. L., TAZELAAR, H. D., SCHROEDER, D. R., OFFORD, K. P.
(1997). Prognostic Significance of Histopathologic Subsets in Idiopathic Pulmonary Fibrosis. Am. J. Respir. Crit. Care Med.
157: 199-203
[Abstract] [Full Text] -
Bois, R M D.
(1994). Fortnightly Review: Diffuse lung disease: an approach to management. BMJ
309: 175-175
[Full Text] -
SOCIETY, B. T., COMMITTEE, S. O. C.
(1990). The Diagnosis, Assessment and Treatment of Diffuse Parenchymal Lung Disease in Adults---British Thoracic Society recommendations. Thorax
54: 1S-28
[Full Text]
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.
