Table 1

Baseline characteristics of the patients at trial entry

VariableMycophenolate mofetil groupCyclophosphamide group
(n=70)(n=70)
Age (years), median (IQR)60 (48–70)61 (53–68)
Paediatric <18 years (%)4 (6)4 (6)
Male sex, n (%)41 (59)33 (47)
Diagnosis, n (%)
 GPA47 (67)44 (63)
 MPA23 (33)26 (37)
ANCA, n (%)
 PR3 or cANCA41 (59)42 (60)
 MPO or pANCA28 (40)26(37)
 Negative1 (1)2 (3)
ANCA ELISA, n (%)
 PR3-ANCA40 (57)42 (60)
 MPO-ANCA27 (39)26 (37)
 Negative3 (4)2 (3)
eGFR at entry (mL/min/m2), median (IQR)
 All patients51 (29–92)51 (31–79)
 Patients with renal disease47 (27–70)46 (29–74)
Organs involvement*, n (%)
 Renal57 (81)57 (81)
 Lung30 (43)35 (50)
 ENT41 (59)38 (54)
BVAS†, median (IQR)19 (13–25)18 (14–23)
CRP (mg/L), median (IQR)22 (7.5–52)19 (5–83)
ESR (mm/hour), median (IQR)54 (31–98)59 (33–90)
Cyclophosphamide prerandomisation
 Patients, n (%)17 (24)22 (31)
 Total dose (g), median (IQR)1 (0.55–1.1)1 (0.6–1.07)
Intravenous methylprednisolone prerandomisation
 Patients, n (%)41 (59)35 (50)
 Total dose (g), median (IQR)1.5 (1.5–3)1.5 (1.5–2)
Plasma exchange prerandomisation
 Patients, n (%)8 (11)4 (6)
 Total exchanges, median (IQR)5 (5–7)7 (6–7)
  • *Renal involvement is defined as one or more renal BVAS items present at entry excluding hypertension alone. Lung and ENT require one or more lung or ENT BVAS items present at entry respectively.

  • †Baseline BVAS data were missing in one subject in the mycophenolate mofetil (MMF) group.

  • ANCA, antineutrophil cytoplasmic antibody; BVAS, Birmingham Vasculitis Activity Score; CRP, C-reactive protein; ENT, ear, nose, throat; ESR, erythrocyte sedimentation rate; GPA, granulomatosis with polyangiitis; MPA, microscopic polyangiitis; MPO, myeloperoxidase; eGFR, estimated glomerular filtration rate.