Benson, F.

Mackie, S.L.

Quick, V.

White Rose Research Online

Letter to the Editor (Other)Life after tocilizumab given for giant cell arteritis: a patient survey and argument for re-treatmentVanessa Quick 1,2,�, Fran Benson2, Sarah L. Mackie 3,4 1Rheumatology Department, Luton and Dunstable University Hospital, Bedfordshire Hospitals NHS Foundation Trust, Bedford, UK 2PMRGCAuk Society, London, UK 3Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, UK 4NIHR Leeds Biomedical Research Centre, Leeds Teaching Hospitals NHS Trust, Leeds, UK�Correspondence to: Vanessa Quick, Department of Rheumatology, Luton and Dunstable Hospital, Lewsey Road, Luton LU4 0DZ, UK. E-mail: v.quick@nhs.netDEAR EDITOR, A recent study (TOC STOP) of 336 patients with GCA living in England, who had completed a course of tocilizumab, showed that up to one-third relapsed within one year of stopping, and up to half relapsed within two years [1]. The National Health Service in England doesn’t currently allow repeat treatment with tocilizumab for GCA patients who relapse [2]. We wanted to find out about the personal experiences of PMRGCAuk Society members with GCA liv-ing in England who had completed a course of treatment with tocilizumab.We therefore created a short survey which could be accessed via a web-link. The Health Research Authority decision tool confirmed that National Health Service research ethics commit-tee approval was not required because patients were identified from the charity’s contact list and website. In December 2023 we emailed the web-link to all PMRGCAuk members with GCA and posted it on the PMRGCAuk patient group section of the HealthUnlocked website asking for experiences we could share with National Health Service funding bodies. We asked three open questions, ‘What was it like being on tocilizumab; what has happened to your GCA and how have you felt since coming off tocilizumab; and would you like access to more toci-lizumab either now or in the future?’. All responses were grouped into themes to create simple statistics, and free-text responses from all patients who had relapsed after tocilizumab cessation were selected to illustrate the patient experience. All patients that completed the survey consented for their data to be used anonymously; those included in Table 1 consented for their free-text responses to be published and approved the final manuscript.Sixteen people responded to the survey. Their responses con-firmed that they had all completed a course of tocilizumab for GCA and did not have access to retreatment. Thirteen of 16 had a positive experience on tocilizumab therapy, with no relap-ses and no reported side effects of the drug. Eight of 16 experi-enced GCA relapse after stopping tocilizumab (Table 1). Three of these relapses would be classified as major relapses defined by EULAR guidelines [3]. Five of 16 reported side effects of treatment, such as prednisolone and conventional synthetic DMARDs (csDMARDs), that were given for GCA after tocili-zumab cessation. Fifteen of 16 wanted access to more tocilizu-mab either now or in the future. All who relapsed after stopping tocilizumab wanted access to retreatment (Table 1).The number of respondents was small and likely not repre-sentative of all GCA patients treated with tocilizumab in England, and the survey questions were open and broad in nature. Nonetheless, the results were remarkably similar to TOC STOP [1]: tocilizumab was effective in >80%; half re-lapsed after stopping tocilizumab; and one-third of relapsers described major relapse. Their experience of tocilizumab was largely positive, whilst experience of relapse after tocilizumab cessation was universally negative, due to recurrent GCA symptoms, need for higher prednisolone dosing, fear of long- term consequences of active disease, and inefficacy of csDMARDs compared with tocilizumab. All those who had relapsed desired access to retreatment, which has been shown in observational studies to quickly recapture GCA remis-sion [4].In 2018, The National Institute of Health and Care Excellence (NICE) published a Technology Appraisal on toci-lizumab for GCA [TA518] [2], based on evidence submitted by Roche Pharmaceuticals, largely from the GiACTA trial [5]. Roche proposed, based on clinical and patient expert opinion, that up to 1 year of tocilizumab treatment would be sufficient to sustain remission in the longer term. At the time the TA518 committee was concerned that this evidence was only based on case reports and that most included no follow- up details. However, both the clinical and patient experts agreed that many patients were likely to need <1 year of toci-lizumab to achieve sustained remission, and that the 1-year stopping rule was acceptable [2].Key message � Tocilizumab retreatment should be an option for GCA relapse after tocilizumab cessation. Accepted: 11 March 2024 # The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology.  This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/ by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com Rheumatology Advances in Practice, 2024, 8(2), rkae054 https://doi.org/10.1093/rap/rkae054 Advance access publication 17 April 2024 Letter to the Editor RheumatologyAdvances in PracticeTable 1. Survey responses from individuals who reported GCA relapse after tocilizumab cessationPatientWhat was it like being on tocilizumab?What has happened to your GCA and how have you felt since coming off tocilizumab?Would you like to have access to more tocilizumab either now or in the future, and why?1It took a few weeks to kick in but I felt so much bet-ter when it did, it’s honestly the only thing that’s helped me.It’s returned I have bouts of GCA again.Yes, because it’s the only treatment that helped.2My whole wellbeing improved. I had faith in this treatment and was grateful for the time I was on it. I wished it would continue but I was aware of the constraints in its use.I have had two relapses when my inflammation markers were raised and I had to increase the prednisone dosage. Following this I began a very slow reduction of prednisolone. On the second re -lapse, I felt really poorly, my mobility was seri-ously limited and had to once again increase the prednisolone dose.Most certainly YES. According to my consultant, they are all in agreement that tocilizumab is the right course of treatment for me and she is trying very hard to get this approved but finding it very difficult to get a positive response.3Fine.Inflammation increased as shown on my PET scan.Yes. I need help to reduce my steroids as I cannot tolerate DMARDs.4I tolerated tocilizumab very well. It took 2-3months to kick in whilst reducing prednisolone dose. I felt very good on it and my energy level improved dramatically.6months after finishing the 12-month course I had a relapse effecting my eyes, jaw and headaches.Yes, as I am severely allergic to DMARD drugs and unable to tolerate them, resulting in hospital treatment. This means there is only prednisolone to treat my condition.5Having had 6months of cyclophosphamide, and high-dose steroids which had me feeling really weakened, ill and anxious that my GCA symp-toms were still not controlled, I was relieved that tocilizumab fairly quickly resolved my symptoms. I felt confident and relieved that at last something was working and working well.I have tried several DMARD drugs, and for various reasons have had to stop them. I’m currently on mycophenolate mofetil but because of deranged liver enzymes, I have had to intermittently stop taking this, resulting in increasing GCA symptoms and the need to increase steroid dose again.Most definitely.6I was able to reduce my prednisolone dosage from 20mg in February 2021 to 4.5mg in August 2022.Within a month my symptoms started to return to the point by October 2022 I was up to 15mg prednisolone again. It is now December 2023 and I am still on 9mg so progress is not great.I would love to restart tocilizumab, if at all possible, in the hope that I can reduce my predniso-lone dose.7I seemed to be getting my life back… far less fa-tigue, fleeting symptoms and better able to man-age everyday type illness like colds. I was able to start reducing steroids below my previous thresh-old. A weekly injection was easy to manage. After struggling for five years on steroids alone, tocili-zumab offered me the option of being ste-roid-free.I needed to go on methotrexate because of a major flare, which does not seem to have the same bene-ficial effects as tocilizumab in its ability to control symptoms at a lower dose of steroids. I have now been diagnosed with steroid-induced pre-type two diabetes and adrenal insufficiency.Yes. I am now steroid-dependent. On tocilizumab, I think I would not be facing the problems I am having now. Also, the current/future demands I will have to make on health and social care serv-ices would be much less. I do not understand why a one-year prescription of tocilizumab is applied to GCA treatment when it is not applied to other illnesses, particularly as the damage suffered by steroids is already known.8I was pretty stable on tocilizumab with no ma-jor flares.I stopped tocilizumab in February 2022, after my one-year allowance ended, and have had several flares since then. I had two strokes later in 2022 that are thought to have been linked to the large vessel vasculitis I have. I have had severe fatigue impacting majorly on my quality of life as well as night sweats and weight loss. I have had to give up work. I had another FDG PET CT in November 2023 and still have inflammation in my aorta, a major concern.I certainly would. This is the only treatment for LVV/GCA with proven efficacy.2                                                                                                                                                                                                                        Letter to the Editor However, there is accumulating evidence, from TOC STOP and other observational studies from around the world [4, 6, 7] that 1 year of treatment is for a substantial propor-tion of patients not ‘enough to sustain remission in the longer term’ as was originally assumed. Relapse often does not occur immediately after tocilizumab cessation, as might have been presumed from the original data. We believe that there is now a strong case to remove the NICE TA518 stipulation that patients prescribed tocilizumab for GCA should ‘not have already had tocilizumab’ [2]. This would ensure that the 50% of patients who relapse after a period of time following tocilizumab cessation are not disadvantaged compared with new starters. This approach would preserve the 1-year stop-ping rule and therefore, based on current evidence, not pro-long treatment unnecessarily for the 50% of patients who may never relapse again. We are aware of several specialist rheumatology centres in England that have obtained local ap-proval to retreat patients who relapse after stopping tocilizu-mab, but this will inevitably lead to inequity which is against the ethos of specialized commissioning. Our small survey provides evidence for the patient's perspective on the current situation and the need for policy change.Data availabilityThe data underlying this article will be shared on reasonable request to the corresponding author.FundingNo specific funding was received from any bodies in the pub-lic, commercial or not-for-profit sectors to carry out the work described in this article.Disclosure statement: V.Q. has received honoraria for educa-tional and/or advisory services or travel support from Novartis, Abbvie, Pfizer, Roche and Fresenius Kabi and is a Trustee of the Charity PMRGCAuk. F.B. has no disclosures. S.L.M. reports: consultancy on behalf of her institution for Roche/Chugai, Sanofi, AbbVie, AstraZeneca, Pfizer; Investigator on clinical trials for Sanofi, GSK, Sparrow; speaking/lecturing on behalf of her institution for Roche/ Chugai, Vifor, Pfizer, UCB, Fresenius Kabi and Novartis; chief investigator on STERLING-PMR trial, funded by NIHR; patron of the charity PMRGCAuk. No personal re-muneration was received for any of the above activities. Support from Roche/Chugai to attend EULAR2019 in person and from Pfizer to attend ACR Convergence 2021 virtually. S.L.M. is supported in part by the NIHR Leeds Biomedical Research Centre. The views expressed in this article are those of the authors and not necessarily those of the NIHR, the NIHR Leeds Biomedical Research Centre, the National Health Service or the UK Department of Health and Social Care.References1. Quick V, Abusalameh M, Ahmed S et al.; “TOC STOP”. Relapse after cessation of weekly tocilizumab for giant cell arteritis: a multi-centre service evaluation in England. Rheumatology (Oxford) 2023; kead604. doi: 10.1093/rheumatology/kead604.2. Nice.org.uk. Tocilizumab for treating giant cell arteritis, NICE tech-nology appraisal guidance. 2018. https://www.nice.org.uk/guid ance/ta518 (13 January 2024, date last accessed).3. Hellmich B, Agueda A, Monti S et al. 2018 Update of the EULAR recommendations for the management of large vessel vasculitis. Ann Rheum Dis 2020;79:19–30.4. Stone JH, Han J, Aringer M et al.; GiACTA Investigators. Long term effect of tocilizumab in patients with giant cell arteritis: open label phase of the Giant Cell Arteritis Actemra (GiACTA) trial. Lancet Rheumatol 2021;3:E328–36.5. Stone JH, Tuckwell K, Dimonaco S et al. Trial of tocilizumab in giant-cell arteritis. N Engl J Med 2017;377:317–28.6. Matza MA, Dagincourt N, Mohan SV et al. Outcomes during and after long-term tocilizumab treatment in patients with giant cell ar-teritis. RMD Open 2023;9:e002923.7. Samec MJ, Rakholiya J, Langenfeld H et al. Relapse risk and safety of long-term tocilizumab use among patients with giant cell arteri-tis: a single-enterprise cohort study. J Rheumatol 2023;50:1310–7.# The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology.This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/ 4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.comRheumatology Advances in Practice, 2024, 8, 1–3https://doi.org/10.1093/rap/rkae054Letter to the EditorLetter to the Editor                                                                                                                                                                                                                        3

Life after tocilizumab given for giant cell arteritis: a patient survey and argument for re-treatment

https://eprints.whiterose.ac.uk/id/eprint/227382/1/Life%20after%20tocilizumab%20given%20for%20giant%20cell%20arteritis%20a%20patient%20survey%20and%20argument%20for%20re-treatment.pdf

Life after tocilizumab given for giant cell arteritis: a patient survey and argument for re-treatment

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