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Ann Intern Med. 2009 May 19;150(10):670-80.

Pulse versus daily oral cyclophosphamide for induction of remission in antineutrophil cytoplasmic antibody-associated vasculitis: a randomized trial.

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1
Klinikum Offenbach, Offenbach, Germany.

Abstract

BACKGROUND:

Current therapies for antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis are limited by toxicity.

OBJECTIVE:

To compare pulse cyclophosphamide with daily oral cyclophosphamide for induction of remission.

DESIGN:

Randomized, controlled trial. Random assignments were computer-generated; allocation was concealed by faxing centralized treatment assignment to providers at the time of enrollment. Patients, investigators, and assessors of outcomes were not blinded to assignment.

SETTING:

42 centers in 12 European countries.

PATIENTS:

149 patients who had newly diagnosed generalized ANCA-associated vasculitis with renal involvement but not immediately life-threatening disease.

INTERVENTION:

Pulse cyclophosphamide, 15 mg/kg every 2 to 3 weeks (76 patients), or daily oral cyclophosphamide, 2 mg/kg per day (73 patients), plus prednisolone.

MEASUREMENT:

Time to remission (primary outcome); change in renal function, adverse events, and cumulative dose of cyclophosphamide (secondary outcomes).

RESULTS:

Groups did not differ in time to remission (hazard ratio, 1.098 [95% CI, 0.78 to 1.55]; P = 0.59) or proportion of patients who achieved remission at 9 months (88.1% vs. 87.7%). Thirteen patients in the pulse group and 6 in the daily oral group achieved remission by 9 months and subsequently had relapse. Absolute cumulative cyclophosphamide dose in the daily oral group was greater than that in the pulse group (15.9 g [interquartile range, 11 to 22.5 g] vs. 8.2 g [interquartile range, 5.95 to 10.55 g]; P < 0.001). The pulse group had a lower rate of leukopenia (hazard ratio, 0.41 [CI, 0.23 to 0.71]).

LIMITATIONS:

The study was not powered to detect a difference in relapse rates between the 2 groups. Duration of follow-up was limited.

CONCLUSION:

The pulse cyclophosphamide regimen induced remission of ANCA-associated vasculitis as well as the daily oral regimen at a reduced cumulative cyclophosphamide dose and caused fewer cases of leukopenia.

PRIMARY FUNDING SOURCE:

The European Union.

TRIAL REGISTRATION:

ClinicalTrials.gov NCT00430105.

PMID:
19451574
[Indexed for MEDLINE]
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