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Tocilizumab for the Treatment of Mevalonate Kinase Deficiency.

1. Introduction

Mevalonate kinase deficiency (MKD) is a rare autosomal recessive autoinflammatory disease caused by mutations in MVK, causing loss of function of the enzyme mevalonate kinase (MVK). Broadly, two clinical phenotypes are recognized that vary in severity as determined by the level of residual enzyme activity. The milder phenotype of MKD is a periodic fever syndrome characterized by frequent episodes of fever typically lasting 3-7 days, abdominal pain, lymphadenopathy, inflammatory eye disease, rashes, and arthralgia [1] and typically associated with intracellular MVK activity greater than 1% [2]. The more severe phenotype is mevalonic aciduria (MA), usually associated with MVK enzyme activity less than 0.5%. MA may result in a high rate of stillbirth; survivors present soon after birth with severe systemic inflammation, facial dysmorphism, severe failure to thrive, developmental delay, seizures, and hepatic involvement [3]. Worldwide, approximately only 300 patients with MKD have been reported [4], including a recent large series from Europe [1].

The pathophysiology of autoinflammation in MKD is poorly understood and is suggested to occur as a result of loss of synthesis of isoprenoid lipids downstream of MVK [5], in particular geranylgeranyl diphosphate. This latter is necessary for prenylation (the addition of a hydrophobic compound) of small GTPases, the loss of which causes activation of the inflammasome and release of IL-1[beta] [6]. More recent studies have indicated a central role for the pyrin inflammasome as the driver of autoinflammation in MKD [7]. There is an inverse relationship between RhoA activation and activation of the pyrin inflammasome: RhoA activation induces downstream kinases, pyrin phosphorylation, and inhibitory binding of phosphorylated pyrin by 14-3-3 proteins [7]. In MKD, deficient geranylgeranylation of RhoA renders it inactive. This is because RhoA activation is dependent on its translocation to the plasma membrane, and this membrane targeting of RhoA is dependent on geranylgeranylation at its C-terminus [7]. Since geranylgeranyl pyrophosphate, the substrate of geranylgeranylation, is a product of the mevalonate pathway, loss-offunction mutations of MVK results in depletion of geranylgeranyl pyrophosphate, failure of Rho membrane binding, and thus persistent RhoA inactivation and consequently pyrin activation which induces IL-1[beta] overproduction in myeloid cells [7, 8]. Thus mutations of MVK lead to release of the normal, constitutive tonic inhibition of the pyrin inflammasome and excess IL-1 production [7].

Consequently, attempts to treat MKD have mainly focused on IL-1 blockade, as reflected in recent international expert consensus guidance [9]. In fact, therapeutic success with IL-1 blockade is at best modest. For anakinra (recombinant interleukin-1 receptor antagonist, blocking IL-1[beta] and IL-1[alpha]), a retrospective series [10] reported only 30% complete remission, and 70% partial remission in patients with MKD treated with daily anakinra. Canakinumab, a monoclonal antibody against IL-1[beta], appears to have superior efficacy to anakinra in retrospective studies, with up to half of patients achieving complete response [10-12]. A major prospective randomised controlled trial of canakinumab (150 mg monthly) for MKD has reported that 35% met a definition of response at 16 weeks; and 45% had a physician global assessment of <2/10 [13]. Since it is now increasingly apparent that MKD is in fact a multicytokinedriven disease, with involvement of other proinflammatory cytokines including IL-6 and tumour necrosis factor-[alpha] (TNF-[alpha]) [14, 15], this somewhat limited efficacy of IL-1 blockade is perhaps unsurprising. It is thus clear that whilst IL-1 blockade may be useful in some patients with MKD, alternative treatments for those who fail to respond adequately to IL-1 blockade are urgently required.

Tocilizumab is a humanised, monoclonal, antihuman IL-6 receptor (IL-6R) antibody that binds to membrane and soluble IL-6R, inhibiting IL-6-mediated signaling [16]. Tocilizumab binds to soluble IL-6R present in serum and joint fluid as well as membrane-bound IL-6R expressed on the surface of cells, leading to inhibition of receptormediated IL-6 signaling and suppression of several physiological roles of IL-6 [16, 17]. Experience of using tocilizumab for the treatment of MKD is limited, with (to date) only six cases reported. We therefore add to these limited data describing a child with MKD who was successfully treated with tocilizumab having failed other treatments and review the literature regarding IL-6 blockade in MKD.

2. Case Presentation

We present the case of a twelve-year-old girl originally from the Faroe Islands with compound heterozygotic MKD (p. V377I/c.417insC), who first presented with symptomatic periodic fever attacks from the age of 3 months. These presented as recurrent episodes of fever (39-41[degrees]C) without infectious cause, occurring once or twice monthly, associated with rigors, pallor, fatigue, lymphadenopathy (inguinal, axillary, and intra-abdominal), abdominal pain, oral ulceration, and arthralgia/myalgia of the lower limbs. Attacks lasted between 3 and 7 days and were accompanied by very high acute phase responses (C reactive protein [CRP] typically greater than 100 mg/L). Attacks were also triggered by vaccinations. Her past medical history included an episode of Stevens-Johnson syndrome in response to penicillin at the age of three years and appendectomy aged 7 years of a normal appendix. She was referred to us in London at the age of 12 years. At that time, she was receiving the anti-TNF[alpha] agent etanercept, which she had been on for the previous 34 months. She had at best only partial response to etanercept in terms of attack severity and duration, but was still missing 100 days per year of school because of attacks which occurred twice a month, lasting for 3 days. In addition, despite etanercept, her inflammatory markers remained significantly raised between attacks: CRP 82 mg/L (reference range [RR] < 10); serum amyloid A (SAA) 1310 mg/L (RR < 10), indicative of severe systemic inflammation in-between attacks and significant risk of reactive AA amyloidosis. Anakinra (2 mg/kg/day; recombinant interleukin-1 receptor antagonist) had also been tried previously, but was complicated both by a severe skin rash and also by the worst disease flare she had ever experienced; hence after four weeks, this was discontinued. Following a six-week washout period from the etanercept (during which she suffered one severe attack), in December 2015 she started intravenous tocilizumab 8 mg/kg every 2 weeks.

After one dose of tocilizumab, her CRP and ESR both rapidly normalised (Figure 1(a)). She had one minor attack with minor, short-lived fleeting rash, but no fever after the first dose. Since normalisation of CRP is a well-known effect of tocilizumab and may occur without necessarily any true improvement in clinical disease activity, we also prospectively used a physician global assessment of disease activity using a 0 to 10 scale, 0 indicating no disease activity and 10 indicating severe disease activity (Figure 1(a)), and change in haemoglobin, white cell count, and platelets (Figure 1(b)) as adjunctive laboratory indicators of successful treatment. In addition, the patient reported significant improvement even after a single dose of tocilizumab, with improved energy levels, reduction in pain, and improvement in oral ulceration. She was also able to return to full-time school.

This excellent clinical and serological response has been sustained for more than 24 months. There have been no reported adverse events. The patient was switched to weekly subcutaneous tocilizumab at 162 mg in June 2016 for ease of administration and reduction in hospital attendances. A year since that change, the patient has had several short-lived flares lasting 1-3 days associated with fever, adenitis, and mouth blistering, but she has not required prednisolone as before and overall expressed a preference for the subcutaneous route as it was associated with improved quality of life despite the breakthrough fever attacks.

3. Discussion

There is no definitive treatment for MKD, and the current rationale for treatment is based on anecdotal case reports, retrospective series, and a limited (albeit increasing) knowledge regarding the pathogenesis of autoinflammation in MKD. The European project, Single Hub and Access point for pediatric Rheumatology in Europe (SHARE), was launched to address this important unmet clinical need and provided a systematic literature review and expert consensus for the treatment of MKD and other autoinflammatory diseases [9]. It is currently suggested that patients with MKD may benefit from treatment with NSAIDs, steroids, and biologics, particularly IL-1 blockade or etanercept. Furthermore, the SHARE guidance emphasizes that statins and colchicine are not effective in MKD [9]. Upon failure of IL-1 blockade and etanercept, IL-6 blockade should be the next biologic instigated, before considering haematopoietic stem cell transplantation (HSCT) [9], although data supporting the use of tocilizumab in MKD are very limited. As such, our case represents (to the best of our knowledge) only the seventh subject with MKD treated with tocilizumab. The efficacy we observed was immediate, dramatic, and sustained over 24 months. This suggests that IL-6 blockade should be given more consideration in patients with MKD, especially after failure of IL-1 blockade is demonstrated.

The biggest series of patients with MKD was recently described from the Eurofever registry [1] providing additional, albeit retrospective data regarding the treatment of MKD. Of note, in that series, 27/114 patients received anakinra: 6/28 (22%) were reported as complete responders; 18/27 (67%) were partial responders; and 11% had no response to anakinra. Anakinra doses are not described in detail in this report, but are likely to be an important factor influencing this (at best) modest efficacy [18]. Canakinumab was given to 5/114 patients and resulted in complete remission in 4/5, with a partial response in the remaining subject [10]. Etanercept was used in 27/114 patients and had a beneficial effect in 16/27 patients (59%), of whom only two (7%) had a complete response [10]. Eleven/27 patients (41%) failed to respond to etanercept [10]. Of note, only 2 patients with severe MKD received tocilizumab, but the treatment responses are not described in any detail in this series [10]. Whilst expert consensus places tocilizumab as an important third-line biologic treatment for MKD [9], there have only been six MKD cases treated with this agent reported worldwide [15,19-21]. The details of these reports are summarized in Table 1.

The pathogenesis of autoinflammation in MKD is poorly understood although recent studies have emphasized that, unlike cryopyrin-associated periodic fever syndromes (CAPS; a purely IL-1-driven autoinflammatory disease), MKD is probably a multicytokine-driven monogenic autoinflammatory disease [2, 5, 15]. One mechanistic model of inflammation in MKD is that of enhanced IL-1[beta] release as a result of decreased Rho/Rac GTPase prenylation, particularly in hyperthermic conditions [5]. Stoffels et al., however, observed an increased cytokine response from cells from MKD patients specific for TLR4, TLR2, and NOD2 stimulation, which included not only IL-1[beta], but also IL-1a, TNFa, and IL-6 [15]. Based on this observation, they questioned whether or not IL-1[beta] is the central driving cytokine in the pathogenesis of MKD. Since they also observed excessive caspase-1 protein in leucocytes from MKD patients, they postulated that this could provide an explanation as to why these cells are more easily triggered to secrete IL-1[beta], but emphasized also that other proinflammatory cytokines are involved. They concluded that this could account for the fact that not all patients respond to blockade of IL-1, as emphasized by the aforementioned results of the only randomised controlled trial published to date [13]. These observations, and the emerging (albeit limited) clinical experience of IL-6 blockade in MKD (Table 1), argue strongly for consideration of IL-6 blockade in MKD, particularly for those who fail to respond adequately to IL-1 blockade [15], but perhaps also for a clinical trial exploring dosing and efficacy of tocilizumab as first-line choice of biologic for MKD. From a practical perspective, tocilizumab is significantly cheaper than canakinumab and avoids the need for daily injections as is the case of anakinra.

The dose and route of administration of tocilizumab for MKD has varied across the published reports (Table 1). Shendi et al. [19] used tocilizumab at an intravenous dose of 8 mg/kg, every four weeks. This is the NICE approved dose for the treatment of rheumatoid arthritis [22] and for some forms of JIA in children weighing [greater than or equal to] 30 kg [23]. This patient went into remission with normalisation of inflammatory markers, but had recurrent upper respiratory tract infections (well described with tocilizumab) [24] necessitating a 50% dose reduction. This lower dose was inadequate to control the MKD however, and was therefore increased again to 7 mg/kg four weekly, with reasonable disease control [19]. We did not observe any infections in our patient, who was treated with 8 mg/kg tocilizumab every two weeks (as per a typical systemic JIA dosing regimen [25]), or latterly whilst on weekly subcutaneous tocilizumab. Regarding this latter point, there are no data that suggest any benefit over intravenous or subcutaneous administration; clearly subcutaneous administration has potential practical advantages, such as avoiding the need for hospital admission for intravenous administration as was the case for a patient.

In conclusion, we report a dramatic and sustained (24 months) clinical and serological response to tocilizumab in a 12-year-old child with MKD, which to the best of our knowledge represents only the seventh patient reported. Since a recent randomised placebo-controlled clinical trial of IL-1 blockade has suggested that more than 50% of patients may fail to respond adequately, we suggest that further consideration should be given to alternative approaches such as IL-6 blockade, particularly for those individuals who fail IL-1 blockade, and especially before considering haematopoietic stem cell transplantation as a therapeutic option.

https://doi.org/10.1155/2018/3514645

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References

[1] N. M. Ter Haar, J. Jeyaratnam, H. J. Lachmann et al., "The phenotype and genotype of mevalonate kinase deficiency: a series of 114 cases from the Eurofever Registry," Arthritis and Rheumatology, vol. 68, no. 11, pp. 2795-2805, 2016.

[2] L. A. Favier and G. S. Schulert, "Mevalonate kinase deficiency: current perspectives," Application of Clinical Genetics, vol. 9, pp. 101-10, 2016.

[3] D. Haas and G. F. Hoffmann, "Mevalonate kinase deficiencies: from mevalonic aciduria to hyperimmunoglobulinemia D syndrome," Orphanet Journal of Rare Diseases, vol. 1, no. 1, p. 13, 2006.

[4] S. Zhang, "Natural history of mevalonate kinase deficiency: a literature review," Pediatric Rheumatology, vol. 14, no. 1, p. 30, 2016.

[5] J. Jurczyluk, M. A. Munoz, O. P Skinner et al., "Mevalonate kinase deficiency leads to decreased prenylation of Rab GTPases," Immunology and Cell Biology, vol. 94, no. 10, pp. 994-999, 2015.

[6] B. Massonnet, S. Normand, R. Moschitz et al., "Pharmacological inhibitors of the mevalonate pathway activate pro-IL-1 processing and IL-1 release by human monocytes," European Cytokine Network, vol. 20, no. 3, pp. 112-120, 2009.

[7] Y. H. Park, G. Wood, D. L. Kastner, and J. J. Chae, "Pyrin inflammasome activation and RhoA signaling in the autoinflammatory diseases FMF and HIDS," Nature Immunology, vol. 17, no. 8, pp. 914-921, 2016.

[8] S. Normand, B. Massonnet, A. Delwail et al., "Specific increase in caspase-1 activity and secretion of IL-1 family cytokines: a putative link between mevalonate kinase deficiency and inflammation," European Cytokine Network, vol. 20, no. 3, pp. 101-107, 2009.

[9] N. M. Ter Haar, M. Oswald, J. Jeyaratnam et al., "Recommendations for the management of autoinflammatory diseases," Annals of the Rheumatic Diseases, vol. 74, no. 9, pp. 1636-1644, 2015.

[10] L. Rossi-Semerano, B. Fautrel, D. Wendling et al., "Tolerance and efficacy of off-label anti-interleukin-1 treatments in France: a nationwide survey," Orphanet Journal of Rare Diseases, vol. 10, no. 1, p. 19, 2015.

[11] N. Ter Haar, H. Lachmann, S. Ozen et al., "Treatment of autoinflammatory diseases: results from the Eurofever Registry and a literature review," Annals of the Rheumatic Diseases, vol. 72, no. 5, pp. 678-685, 2013.

[12] C. Galeotti, U. Meinzer, P. Quartier et al., "Efficacy of interleukin-1-targeting drugs in mevalonate kinase deficiency," Rheumatology, vol. 51, no. 10, pp. 1855-1859, 2012.

[13] F. De Benedetti, J. Anton, M. Gattorno et al., "A Phase III pivotal umbrella trial of canakinumab in patients with autoinflammatory periodic fever syndromes (cochicene resistant FMF, HIDS/MKD and TRAPS)," Annals of the Rheumatic Diseases, vol. 75, no. 2, p. 615, 2016.

[14] J. P. Drenth, M. van Deuren, J. van der Ven-Jongerkrijg et al., "Cytokine activation during attacks of hyperimmunoglobulinemia D and periodic fever syndrome," Blood, vol. 85, no. 12, pp. 3586-3593, 1995.

[15] M. Stoffels, J. Jongekrijg, T. Remijn, N. Kok, J. W. M. van der Meer, and A. Simon, "TLR2/TL.R4dependent exaggerated cytokine production in hyperimmunoglobulinaemia D and periodic fever syndrome," Rheumatology, vol. 54, no. 2, pp. 363-368, 2015.

[16] M. Mihara, K. Kasutani, M. Okazaki et al., "Tocilizumab inhibits signal transduction mediated by both mIL-6R and sIL-6R, but not by the receptors of other members of IL-6 cytokine family," International Immunopharmacology, vol. 5, no. 12, pp. 1731-40, 2005.

[17] N. Nishimoto and T. Kishimoto, "Humanized antihuman IL6 receptor antibody, tocilizumab," in Handbook of Experimental Pharmacology, vol. 181, pp. 151-60, Springer, Berlin, Germany, 2008.

[18] R. Campanilho-Marques and P. Brogan, "Mevalonate kinase deficiency in two sisters with therapeutic response to anakinra: case report and review of the literature," Clinical Rheumatology, vol. 33, no. 11, pp. 1681-1684, 2014.

[19] H. M. Shendi, L. A. Devlin, and J. D. Edgar, "Interleukin 6 blockade for hyperimmunoglobulin D and periodic fever syndrome," Journal of Clinical Rheumatology, vol. 20, no. 2, pp. 103-105, 2014.

[20] T. Lane, J. D. Gillmore, A. D. Wechalekar, P. N. Hawkins, and H. J. Lachmann, "Therapeutic blockade of interleukin-6 by tocilizumab in the management of AA amyloidosis and chronic inflammatory disorders: a case series and review of the literature," Clinical and Experimental Rheumatology, vol. 33, no. 94, pp. S46-S53, 2015.

[21] A. Muster, P. P. Tak, D. L. P. Baeten, and S. W. Tas, "Antiinterleukin 6 receptor therapy for hyper-IgD syndrome," BMJ Case Reports, vol. 2015, p. bcr2015210513, 2015.

[22] National Institute for Health and Care Excellence (NICE), Adalimumab, Etanercept, Infliximab, Certolizumab Pegol, Golimumab, Tocilizumab and Abatacept for Rheumatoid Arthritis not Previously Treated with DMARDs or After Conventional DMARDs Only Have Failed, NICE Technology Appraisal Guidance, NICE, London, UK, 2016.

[23] National Institute for Health and Care Excellence (NICE), Abatacept, Adalimumab, Etanercept and Tocilizumab for Treating Juvenile Idiopathic Arthritis, NICE Technology Appraisal Guidance, NICE, London, UK, 2015.

[24] F. De Benedetti, H. I. Brunner, N. Ruperto et al., "Randomized trial of tocilizumab in systemic juvenile idiopathic arthritis," New England Journal of Medicine, vol. 367, no. 25, pp. 2385-95, 2012.

[25] National Institute for Health and Care Excellence (NICE), Tocilizumab for the Treatment of Systemic Juvenile Idiopathic Arthritis, NICE Technology Appraisal Guidance, NICE, London, UK, 2011.

Nadia K. Rafiq, (1) Helen Lachmann, (2) Frodi Joensen, (3) Troels Herlin, (4) and Paul A. Brogan (1)

(1) Infection and Inflammation and Rheumatology Section, University College London Great Ormond Street Institute of Child Health, 30 Guilford Street, London WC' E'H, UK

(2) National Amyloidosis Centre, University College London Division of Medicine, London, UK

(3) National Hospital of the Faroe Islands, J. C. Svabos Gota, Torshavn '00, Faroe Islands

(4) Department of Paediatrics, Pediatric Rheumatology Clinic, Palle Juul-Jensens Boulevard 99, 8200 Aarhus N, Denmark

Correspondence should be addressed to Nadia K. Rafiq; n.rafiq@nhs.net

Received 3 May 2018; Accepted 18 July 2018; Published 26 August 2018

Academic Editor: Ozgur Cogulu

Caption: Figure 1: (a) Change in clinical disease activity inflammatory markers in response tocilizumab. Note. PGA: physician global assessment, 0-10,0 indicating absence of disease activity and 10 indicating severe disease. ESR: erythrocyte sedimentation rate. CRP: C reactive protein. PGA fell from 8/10 immediately before the first tocilizumab infusion to 1/10 when assessed immediately prior to the next infusion 2 weeks later. This excellent clinical and serological response has been sustained for 24 months. (b) Change in haemoglobin, total white cell count, and platelet count in response to tocilizumab. Black arrow shows date of first dose of tocilizumab.
Table 1: Previous reports of tocilizumab for the treatment of MKD.

                       Shendi et al.     Stoffels et al.
                       (n = 1) [19]      (n = 2) [15]

Patient                1                 2            3

TOC dose (mg/kg) and   7 IV              8 IV         8 IV
route of
administration

Frequency of           4                 4            4
administration
(weeks)

Age (range), years     13                Not          Not
at onset of TOC                          described    described

Treatment prior to     COL PRED          ANA          ANA
TOC                    ETA ANA

Duration of            20                5            5
treatment (months)

Outcome Clinical       CR                CR           CR

Serological            CR                Not          PR
                                         described

Adverse events         URTI              Not          Not
                                         described    described

Comments               CR at dose of 8   --           --
                       mg/kg but due
                       to adverse
                       events dose
                       reduced,
                       ultimately with
                       stable clinical
                       and serological
                       status on 7 mg/
                       kg IV every 4
                       weeks

                       Lane et al. (n= 2) [20]   Muster et al.
                                                 (n = 1) [21]

Patient                4            5            6

TOC dose (mg/kg) and   8 IV         8 IV         8 IV
route of
administration

Frequency of           4            4            4
administration
(weeks)

Age (range), years     24           13           36
at onset of TOC

Treatment prior to     ANA ETA      ETA          NSAID
TOC                                              SIMVA ANA

Duration of            24           13           48-60
treatment (months)

Outcome Clinical       CR                        PR

Serological            CR                        --

Adverse events         Not                       Not
                       described                 described

Comments               MKD          Stabilized   After
                       complicated  on           starting
                       by AA        monotherapy  TOC,
                       amyloidosis. with TOC     average
                       Remained                  hospital
                       on therapy                admissions
                       with PRED                 dropped
                       0.5 mg/                   11/yr to
                       kg/day                    3/yr TOC
                                                 given in
                                                 combination
                                                 with IVMP
                                                 for first
                                                 3 yrs then
                                                 as
                                                 monotherapy

IV: intravenous; COL: colchicine; PRED: prednisolone; ETA:
etanercept; ANA: anakinra; NSAID: nonsteroidal anti-inflammatory
drug; SIMVA: simvastatin; CR: complete response; PR: partial
response; URTI: upper respiratory tract infection; TOC: tocilizumab;
yrs: years.
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Title Annotation:Case Report
Author:Rafiq, Nadia K.; Lachmann, Helen; Joensen, Frodi; Herlin, Troels; Brogan, Paul A.
Publication:Case Reports in Pediatrics
Geographic Code:4EUUK
Date:Jan 1, 2018
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