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P184 Developing a pathway for tocilizumab treatment in giant cell arteritis: a South London regional experience
Abstract Background Tocilizumab is now approved by the National Institute of Health and Care Excellence (NICE) for up to a year in relapsing or refractory giant cell arteritis (GCA). The practicalities of developing a pathway for referral using a hub and spoke model were previously unknown. Here we...
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Published in: | Rheumatology (Oxford, England) England), 2020-04, Vol.59 (Supplement_2) |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | Abstract
Background
Tocilizumab is now approved by the National Institute of Health and Care Excellence (NICE) for up to a year in relapsing or refractory giant cell arteritis (GCA). The practicalities of developing a pathway for referral using a hub and spoke model were previously unknown. Here we discuss our novel experiences utilising tocilizumab for GCA in its first year of licensing, after the introduction of a new regional multi-disciplinary team referral pathway.
Methods
We assessed all patients started on tocilizumab for GCA between August 2018-May 2019. The central assessing hub is St George’s University Hospitals NHS Foundation Trust, a large tertiary rheumatology department in the South of England, serving a population of 1.3 million.
Results
As per Table 1 below. A total of 9 patients were identified: 6 female and 3 male, with an average age of 74.2 (range 63-80). 5 patients were referred internally from clinicians at St George’s Hospital, with the remainder from local district general hospitals. Steroid protocols between patients were varied, and two-thirds required a 3-day IV methylprednisolone course, including all 4 patients with visual symptoms. A third of patients were on concurrent methotrexate, a disease-modifying antirheumatic drug. 8 of 9 patients were on alendronate, vitamin D/calcium, and a gastroprotective agent, and 7 were on aspirin. Reported side effects from steroids were common, with weight gain, increased appetite and osteoporosis noted. All our 9 patients continue their tocilizumab injections, with one individual having a 3-month break for a routine hip operation, and another a 1-month hiatus due to temporary derangement in liver function tests. Tocilizumab proffered improved disease control and few side effects were noted. 3 patients have now been on tocilizumab for 12 months and raise interesting discussions about ongoing funding and treatment efficacy.
P184 Table 1:
Data collected from 9 patients with giant cell arteritis on tocilizumab treatment
Patient number
1
2
3
4
5
6
7
8
9
Age
78
78
74
74
78
80
73
70
63
Sex
M
M
M
F
F
F
F
F
F
Duration of GCA disease (months)
10
11
10
31
80
72
15
14
171
Steroid dose at start of TOC (mg)
50
20
40
20
25
10
60
40
-
Most recent steroid dose (mg) and date
20mg, May 2019
20mg, Jun 2019
17.5mg, Sep 2019
6mg, Jun 2019
6mg, Aug 2019
4mg, Oct 2019
7mg, Jul 2019
-
5mg, Jul 2019
Months on TOC (as of Oct 2019)
7
4
4
7
12
11
12
12
-
Concurrent DMARDs and dose
MTX 10mg qw
-
-
MTX 15mg qw
-
-
-
-
MTX |
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ISSN: | 1462-0324 1462-0332 |
DOI: | 10.1093/rheumatology/keaa111.179 |