ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 885

a Retrospective Analysis of Low Dose Cyclophosphamide Therapy in Systemic Vasculitides

Antigoni Grigoriou1, Shirish Sangle2, Chai Ling2 and David P. D'Cruz3, 1Rheumatology, St George's Univeristy Hospitals NHS Foundation Trust, London, United Kingdom, 2Louise Coote Lupus Unit, Guy's and St Thomas' Hospital, London, UK, London, United Kingdom, 3Louise Coote Lupus Unit, Guy's and St Thomas' Hospital, London, United Kingdom

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: Cyclophosphamide and vasculitis

  • Tweet
  • Email
  • Print
Session Information

Date: Sunday, November 8, 2015

Title: Vasculitis Poster I

Session Type: ACR Poster Session A

Session Time: 9:00AM-11:00AM

Background/Purpose:

The ‘Euro-Lupus’ low dose cyclophosphamide (CPM) protocol has been validated for use in lupus nephritis patients in randomised controlled trials. A recent controlled study of this protocol by the French vasculitis group has shown favourable results in ANCA positive vasculitis. Our aim is to assess the efficacy and safety of low dose CPM in systemic vasculitides patients.

Methods:

We retrospectively assessed 26 patients with systemic vasculitis at the Louise Coote lupus Unit at Guy’s and St Thomas’ Hospital who received low dose CPM induction therapy along with corticosteroids during the last 15 years. All patients fulfilled the ACR/Chapel Hill classification criteria for Granulomatosis with Polyangiitis, eosinophilic Granulomatosis with Polyangitis and Microscopic Polyangitis. All patients received 3 pulses of methylprednisolone 500mg and 6 pulses of CPM infusion 500 mg with mesna fortnightly as induction therapy. Subsequently Azathioprine, Methotrexate or Mycofenolate Mofetil were used as remission maintaining agents. Data regarding inflammatory markers Erythrocyte Sedimentation Rate (ESR) and C-reactive protein (CRP), Birmingham Vasculitis Activity Score (BVAS) and Vasculitis Damage Index (VDI) scores were assessed at baseline and after 6, 12, 24, 60, 120 and 180 months. Data on all relapses, organ involvement, duration of remission, corticosteroid requirement, repeat CPM infusions, Rituximab and adverse events were recorded.

Results:

26 patients (13 males, 13 females) were assessed. 22 were Caucasians, 2 mixed ethnicity and 2 Asians. Median age was 54 years. 20 patients had positive ANCA antibodies (15 anti-PR3, 5 anti-MPO). 6 were ANCA negative. The median disease duration prior to induction therapy was 3.12 years.  10 patients had  pulmonary involvement (pulmonary hemorrhages, haemoptysis, cavitating lung lesions, nodules),  9 necrotizing crescentic glomerulonephritis, 1 myocarditis, 7 neurological manifestations (raised ICP, occipital masses, mononeuritis multiplex), 3 orbital granulomas, 1 necrotizing scleritis, 2 otitis media with hearing loss and 1 bowel ischaemia. Co-morbidities were antiphospholipid syndrome (2 patients), positive lupus anticoagulant (2), type 2 diabetes mellitus (1), past Tuberculosis (1) and sleep apnoea (1). All patients received tapered doses of oral prednisolone (median dose 30 mg) following the induction regimen.

Median duration of remission was 2.40 years. There was improvement in BVAS, CRP and ESR. 10 patients had relapses over 5 years. 5 patients required repeat CPM pulses for flares and 7 received Rituximab. 12 adverse events were recorded. Renal function remained stable over the years. 1 death has been recorded (See Table)

Conclusion:

Low dose intravenous infusion of CPM in combination with steroids may be  effective in achieving remission in systemic vasculitides. This regimen may have fewer adverse events than conventional therapy with high dose CPM.

Table: 

Time (1/12=1month)

Pre therapy 

6/12

12/12

24/12

60/12

120/12

180/12

BVAS

15.52

(n=23)

4.54 (n=22)

5.42

(n=19)

9.00

 (n=9)

4.40

(n=5)

2.00 (n=3)

2.00 (n=2)

ESR (mm/hr)

28.77

(n=22)

18.26

(n=19)

24.52

(n=17)

31.00

 (n=6)

9.60

 (n=5)

8.50 (n=2)

8.50 (n=2)

CRP (mg/L)

45.54

(n=22)

15.21

(n=19)

12.84

(n=19)

16.50

(n=6)

7.60

(n=5)

1.00 (n=2)

1.00 (n=2)

Creatinine

(umol/L)

84.52

(n=21)

91.50

(n=20)

94.20 (n=20)

107.28

(n=7)

105.83

(n=6)

129.50

(n=2)

139.00

(n=2)

e GFR (ml/min)

79.15

(n=20)

76.56

(n=16)

74.78

(n=18)

67.50

(n=8)

70.75

(n=4)

46.00 (n=2)

44.00 (n=2)

PCR

72.44

(n=16)

20.75

(n=12)

17.62

(n=8)

31.00

 (n=4)

0

(n=1)

342.00

(n=1)

181.00

(n=1)

Remission

(BVAS =0)

 

N=4

N=3

N=1

N=1

N=1

N=1

Prednisolone

dose (mg)

30

(n=21)

14

(n=20)

13

(n=21)

14

 (n=8)

9 (

n=5)

6 (n=2)

7.5 (n=2)

Relapses

 

N=2

N=5

N=1

N=2

 

N=1

Rituximab therapy 

 

N=2

N=3

N=2

 

N=1

 

Repeat CYP therapy

 

N=3

N=2

N=1

 

 

 

VDI (median)

1.76 (n=21)

2.60 (n=20)

2.67

 (n=18)

3.62

(n=8)

2.4

(n=5)

1.33 (n=3)

1.00 (n=2)

Adverse events

 

UTIs (recurrent) (n=1), SCC

(n=1), cataract (n=1)

Reactivation of variccella zoster/

Shingles (n=1)

Death (n=1),

steroid induced diabetes/

pancreatitis (n=1)

Squamous cell carcinoma (n=1)

MI (n=1)

Hurtle cell tumour (n=1


Disclosure: A. Grigoriou, None; S. Sangle, None; C. Ling, None; D. P. D'Cruz, None.

To cite this abstract in AMA style:

Grigoriou A, Sangle S, Ling C, D'Cruz DP. a Retrospective Analysis of Low Dose Cyclophosphamide Therapy in Systemic Vasculitides [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/a-retrospective-analysis-of-low-dose-cyclophosphamide-therapy-in-systemic-vasculitides/. Accessed .
  • Tweet
  • Email
  • Print

« Back to 2015 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/a-retrospective-analysis-of-low-dose-cyclophosphamide-therapy-in-systemic-vasculitides/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology