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Long-Term Follow-Up of Cyclophosphamide Compared with Azathioprine for Initial Maintenance Therapy in ANCA-Associated Vasculitis.

Walsh, Michael ; Faurschou, Mikkel ; Berden, Annelies ; Flossmann, Oliver ; Bajema, Ingeborg ; Höglund, Peter LU ; Smith, Rona ; Szpirt, Wladimir ; Westman, Kerstin LU and Pusey, Charles D , et al. (2014) In Clinical Journal of the American Society of Nephrology 9(9). p.1571-1576
Abstract
Treatment with azathioprine within 3 months of remission induction with cyclophosphamide is a common treatment strategy for patients with ANCA-associated vasculitis. This study comprised patients undergoing long-term follow-up who were randomly allocated to azathioprine after 3-6 months or after 12 months of cyclophosphamide treatment.DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Patients from 39 European centers between 1995 and 1997 with a new diagnosis of ANCA-associated vasculitis that involved the kidneys or another vital organ were eligible. At the time of diagnosis, participants were randomly allocated to convert to azathioprine after 3-6 months (the azathioprine group) or after 12 months of cyclophosphamide (the... (More)
Treatment with azathioprine within 3 months of remission induction with cyclophosphamide is a common treatment strategy for patients with ANCA-associated vasculitis. This study comprised patients undergoing long-term follow-up who were randomly allocated to azathioprine after 3-6 months or after 12 months of cyclophosphamide treatment.DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Patients from 39 European centers between 1995 and 1997 with a new diagnosis of ANCA-associated vasculitis that involved the kidneys or another vital organ were eligible. At the time of diagnosis, participants were randomly allocated to convert to azathioprine after 3-6 months (the azathioprine group) or after 12 months of cyclophosphamide (the cyclophosphamide group). Patients who did not achieve a remission within 6 months were excluded. This study assessed relapses, ESRD, and death during long-term follow-up.RESULTS: Patients were allocated to the azathioprine group (n=71) and the cyclophosphamide group (n=73). Of these patients, 63 (43.8%) developed a relapse, 35 (24.3%) developed a renal relapse, 13 (9.0%) developed ESRD, and 21 (14.6%) died. Although there were worse outcomes in the azathioprine group, none were statistically significant. The subdistribution hazard ratio [sHR] for relapse was 1.63 (95% confidence interval [95% CI], 0.99 to 2.71), the composite of relapse or death hazard ratio [HR] was 1.59 (95% CI, 1.00 to 2.54), the ESRD sHR was 1.71 (95% CI, 0.56 to 5.19), and the death HR was 0.75 (95% CI, 0.32 to 1.79).CONCLUSIONS: It remains uncertain whether converting to azathioprine after 3-6 months of induction cyclophosphamide therapy is as effective as converting after 12 months. Outcomes are still poor for this group of patients and further research is required to determine the optimal timing of maintenance therapy. (Less)
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publishing date
type
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publication status
published
subject
in
Clinical Journal of the American Society of Nephrology
volume
9
issue
9
pages
1571 - 1576
publisher
Amer Soc Nephrology
external identifiers
  • pmid:24970876
  • wos:000341275200012
  • scopus:84922202111
  • pmid:24970876
ISSN
1555-905X
DOI
10.2215/CJN.00100114
language
English
LU publication?
yes
id
2facb16a-ccc4-406b-8430-34a18a0965c8 (old id 4526686)
alternative location
http://www.ncbi.nlm.nih.gov/pubmed/24970876?dopt=Abstract
date added to LUP
2016-04-01 11:14:14
date last changed
2022-04-20 18:02:06
@article{2facb16a-ccc4-406b-8430-34a18a0965c8,
  abstract     = {{Treatment with azathioprine within 3 months of remission induction with cyclophosphamide is a common treatment strategy for patients with ANCA-associated vasculitis. This study comprised patients undergoing long-term follow-up who were randomly allocated to azathioprine after 3-6 months or after 12 months of cyclophosphamide treatment.DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Patients from 39 European centers between 1995 and 1997 with a new diagnosis of ANCA-associated vasculitis that involved the kidneys or another vital organ were eligible. At the time of diagnosis, participants were randomly allocated to convert to azathioprine after 3-6 months (the azathioprine group) or after 12 months of cyclophosphamide (the cyclophosphamide group). Patients who did not achieve a remission within 6 months were excluded. This study assessed relapses, ESRD, and death during long-term follow-up.RESULTS: Patients were allocated to the azathioprine group (n=71) and the cyclophosphamide group (n=73). Of these patients, 63 (43.8%) developed a relapse, 35 (24.3%) developed a renal relapse, 13 (9.0%) developed ESRD, and 21 (14.6%) died. Although there were worse outcomes in the azathioprine group, none were statistically significant. The subdistribution hazard ratio [sHR] for relapse was 1.63 (95% confidence interval [95% CI], 0.99 to 2.71), the composite of relapse or death hazard ratio [HR] was 1.59 (95% CI, 1.00 to 2.54), the ESRD sHR was 1.71 (95% CI, 0.56 to 5.19), and the death HR was 0.75 (95% CI, 0.32 to 1.79).CONCLUSIONS: It remains uncertain whether converting to azathioprine after 3-6 months of induction cyclophosphamide therapy is as effective as converting after 12 months. Outcomes are still poor for this group of patients and further research is required to determine the optimal timing of maintenance therapy.}},
  author       = {{Walsh, Michael and Faurschou, Mikkel and Berden, Annelies and Flossmann, Oliver and Bajema, Ingeborg and Höglund, Peter and Smith, Rona and Szpirt, Wladimir and Westman, Kerstin and Pusey, Charles D and Jayne, David R W}},
  issn         = {{1555-905X}},
  language     = {{eng}},
  number       = {{9}},
  pages        = {{1571--1576}},
  publisher    = {{Amer Soc Nephrology}},
  series       = {{Clinical Journal of the American Society of Nephrology}},
  title        = {{Long-Term Follow-Up of Cyclophosphamide Compared with Azathioprine for Initial Maintenance Therapy in ANCA-Associated Vasculitis.}},
  url          = {{http://dx.doi.org/10.2215/CJN.00100114}},
  doi          = {{10.2215/CJN.00100114}},
  volume       = {{9}},
  year         = {{2014}},
}