Discovery of Innovative Therapies for Rare Immune-Mediated Inflammatory Diseases via Off-Label Prescription of Biologics: The Case of IL-6 Receptor Blockade in Castleman’s Disease
- Amsterdam Rheumatology and immunology Center; Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands
Biologics have revolutionized the field of clinical immunology and proven to be both effective and safe in common immune-mediated inflammatory diseases (IMIDs) such as rheumatoid arthritis, inflammatory bowel diseases, and various hematological disorders. However, in patients with rare, severe IMIDs failing on standard therapies, it is virtually impossible to conduct randomized controlled trials. Therefore, biologics are usually prescribed off-label in these often severely ill patients. Unfortunately, off-label prescription is sometimes hampered in these diseases due to a lack of reimbursement that is often based on a presumed lack of evidence for effectiveness. In the present article, we will discuss that off-label prescription of biologics can be a good way to discover new treatments for rare diseases. This will be illustrated using a case of multicentric Castleman’s disease, an immune-mediated lymphoproliferative disorder, in which off-label tocilizumab (humanized anti-IL-6 receptor blocking antibody) treatment resulted in remarkable clinical improvement. Furthermore, we will give recommendations for monitoring efficacy and safety of biologic treatment in rare IMIDs, including the use of registries. In conclusion, we put forward that innovative treatments for rare IMIDs can be discovered via off-label prescription of biologicals, provided that this is based on rational arguments including knowledge of the pathophysiology of the disease.
In patients with rare, severe immune-mediated inflammatory diseases (IMIDs), biologics are often the last treatment option when standard therapy with classical immunosuppressive drugs fails. However, clear guidelines on biologic prescription in these diseases are often lacking. A major reason is that proper randomized controlled trials (RCTs) are difficult to design due to the low prevalence, heterogeneity of patients, and the severe medical condition of patients. Since RCTs are usually required for registration of therapy for a specific disease, physicians often prescribe biologics off-label in these diseases (1). Off-label prescription can be defined as the prescription of a drug for conditions other than current registered indications. This means that the drug is approved by either FDA or EMA for a certain disease, yet there is no definitive proof for the efficacy of the specific drug for other conditions. The physician’s decision to prescribe off-label in such cases is often based on the pathophysiology of the disease or shared symptoms with other diseases in which the biologic has proven to be effective. This is called rational prescription and may lead to innovative treatment options, especially in rare diseases. We will illustrate this in the present article by discussing the case of Castleman’s disease (CD) and interleukin (IL)-6 receptor blockade, including a case report of a patient who responded very well to this treatment strategy. In addition, we provide an overview of current new developments toward responsible off-label use of biologics in rare, severe, and therapy-refractory IMIDs.
Castleman’s Disease: Clinical Symptoms and the Role of IL-6
Castleman’s disease is a rare and relatively unknown lymphoproliferative disorder. It is characterized by polyclonal B-cell proliferation, usually associated with autoimmune and connective tissue symptoms, and often goes together with a pre-existing autoimmune disorder, such as rheumatoid arthritis (RA), Sjögren’s syndrome, and systemic lupus erythematodes (SLE) (2).
Castleman’s disease can be divided into unicentric Castleman’s disease (UCD) and multicentric Castleman’s disease (MCD). In UCD, a single lymphoid region is involved, in contrary to the latter in which multiple lymphoid regions are involved (3). UCD usually causes complaints resulting from enlargement of one or more lymph nodes and mostly lacks systemic symptoms (2). Removal of the lymph node cures 90% of the patients without further complications (4). MCD, on the other hand, can cause “B symptoms” and signs such as anorexia, anemia, and low white blood cell counts (3). MCD has been associated with HIV infection, which is similar to MCD observed in non-HIV-infected patients, except for the high prevalence of pulmonary symptoms and strong association with Kaposi’s sarcoma. Interestingly, also HHV-8, a virus causing Kaposi’s sarcoma, is also associated with MCD (5). Both UCD and MCD are characterized by hypersecretion of IL-6, most likely by germinal center B-cells in hyperplastic lymph nodes. Furthermore, a correlation between serum IL-6 levels and clinical symptoms of patients with CD was shown (6). IL-6 regulates T-cell function, acute phase reaction, and terminal B-cell differentiation (2). Overproduction of IL-6 can cause various symptoms, including fever and lymphadenopathy, and has been associated with autoimmune disorders, such as RA and juvenile idiopathic arthritis (JIA), as well as lymphoid malignancies (7). The prognosis for MCD is usually better when diagnosed early. Yet, early diagnosis can be very challenging because of the common manifestation of lymph node enlargement in patients with various autoimmune disorders. Moreover, diagnosing MCD can sometimes be hard, because symptoms are often not very specific. Nonetheless, CD should be suspected when a patient’s primary diagnosed disease, such as another lymphoproliferative disease or autoimmune disease is unusually hard to treat (8).
Treatment of Castleman’s Disease
Corticosteroids are given as standard therapy in CD, usually resulting in improvement of symptoms, normalization of laboratory parameters, and regression of lymphadenopathy (2, 4). However, relapses are often seen after tapering the dose. Other treatment options are combination chemotherapy and the use of lenalidomide/thalidomine (4). Biologics have also been used in the treatment of CD. Rituximab (chimeric anti-CD20 monoclonal antibody) may be effective, especially in CD patients with pre-existent autoimmune disease (9). Interestingly, long-term remission has also been reported after rituximab administration (2). Clinical improvement after rituximab treatment has been associated with reduced serum levels of pro-inflammatory cytokines, including IL-6 (10). The following case report illustrates the challenges in the treatment of MCD and the potential benefit of rational off-label prescription of biologics in rare IMIDs. In accordance with Dutch laws, the patient gave written informed consent to both the off-label treatment with tocilizumab and the use of his case for this manuscript.
A 63-year-old male patient was referred with lymphadenopathy, limb pain, weight loss, and night sweats. Infectious causes and lymphoma were excluded. Eventually, he was diagnosed with MCD, based on clinical manifestations in combination with results of lymph node and bone marrow biopsies demonstrating polyclonal B-cell proliferation. HHV-8 and HIV tests were negative. After failing to respond to high-dose prednisolone treatment, rituximab was administered, dosed in a cycle of 1000 mg intravenously twice every 6 months, which eventually led to a stable condition for 2 years. However, the disease recurred with extensive lymphadenopathy and strongly elevated erythrocyte sedimentation rate (ESR) levels. In addition, he experienced severe weight loss (10 kg), nausea, loss of appetite, increased muscle pain, and extreme fatigue, resulting in disability. Based on the important role of IL-6 in the biology of B-cells, elevated IL-6 levels in patients with CD, and case reports, tocilizumab (anti-IL-6 receptor antibody) treatment was initiated (600 mg biweekly intravenously) combined with methotrexate (7.5 mg weekly). This resulted in a marked decrease in C-reactive protein (CRP) and ESR levels, normalization of hemoglobin (Hb) (Figure 1) and albumin levels and remarkable clinical improvement (weight gain and improvement in overall physical condition). In addition, there was a significant reduction of the lymphadenopathy. Lowering the frequency of tocilizumab administration was not possible as this resulted in immediate flaring of the disease. Subsequent increased dosing induced remission again.
Figure 1. Inflammatory parameters and hemoglobin levels in time. Red line indicates start tocilizumab therapy.
IL-6 Blockade in Castleman’s Disease
As already mentioned, IL-6 overproduction is associated with the pathogenesis of CD and IL-6 signaling can be blocked by tocilizumab, a humanized monoclonal antibody directed against the human IL-6 receptor. Tocilizumab is used in the treatment of chronic inflammatory diseases in which IL-6 has been implicated in the pathogenesis and exerts its effects by neutralizing the pro-inflammatory effects of IL-6/IL-6 receptor signaling. In addition, tocilizumab treatment may increase the proportion and function of regulatory T cells in the peripheral blood, as has been described in RA (11, 12).
Like most other biologics, the use of tocilizumab is associated with a moderately increased risk of infection. Furthermore, patients sometimes exhibit a transient hypercholesterolemia. Tocilizumab is an effective and safe officially approved treatment for RA and JIA. We describe the successful treatment of a patient with CD with tocilizumab. Over the past few years, several other reports have also described as a good outcome of IL-6 receptor blockade in patients with CD. Nishimoto et al. report an open-label study of 28 patients with MCD. Patients were treated biweekly with 8 mg/kg of tocilizumab for 16 weeks, resulting in improvement of symptoms, reduced acute phase reactants, and decreased need for corticosteroids (13). Interestingly, a recent paper reported persistent improvement of anemia in CD after the administration of tocilizumab. Twelve months after tocilizumab administration, iron-related parameters normalized and symptoms improved in all nine patients (14). This can be explained by the role of IL-6 as inducer of hepcidin, a principal regulator of iron homeostasis (15). Tocilizumab blocks the IL-6 receptor and indirectly downregulates hepcidin. This results in a decrease of iron storage and therefore an increase of serum iron available for Hb synthesis and erythrocyte production, leading to a normalization of the anemia in MCD (2, 14).
As described here, tocilizumab can be very effective in patients with this condition who do not respond to conventional treatment (16). In Japan, these findings have led to the approval and registration of tocilizumab for the treatment of CD (2, 16). However, in many other countries, including the Netherlands and the USA, tocilizumab has not been approved for the treatment of CD and is therefore often not reimbursed.
Rational Prescription of Biologics and Monitoring Off-Label Use
This case report illustrates that off-label prescription is sometimes the only option left after failure of all other possible treatments and can be very effective. Importantly, off-label prescription of biologics should preferably be “rational,” i.e., prescription of an approved drug proven to be safe and effective in a certain disease for another disease based on shared signs and symptoms or knowledge on the pathophysiology of the disease. The present case is a good example of rational prescription, as the initiation of tocilizumab treatment was mainly based on the important role of IL-6 in the pathophysiology of CD. Other examples of this are the use of anti-TNF biologics in TNF-driven diseases or the prescription of IL-1 receptor antagonists in autoinflammatory diseases that are characterized by derailed IL-1-dependent intracellular processes (1).
Obviously, it is crucial to carefully monitor efficacy and safety of biologics that are prescribed off-label (1). This is not only important for individual patients but also for generating more evidence to eventually support reimbursement of novel off-label treatments for rare IMIDs; especially since healthcare authorities often decide that off-label prescription of these expensive drugs is not reimbursed due to “lack of evidence” for efficacy in rare IMIDs, which may prevent physicians from prescribing biologics in these patients. We therefore advocate improved monitoring and reporting off-label use of biologics through registries. In several countries, registries have been set up that have provided important information on safety and efficacy in a variety of conditions (17). For example, the RUBRIC registry (acronym for Rational Use of Biologics in Refractory Immune-mediated inflammatory diseases Consortium) is a web-based registry in the Netherlands aiming to identify and monitor all patients suffering from rare therapy-refractory IMIDs who are treated off-label with biologics (18). The information that is generated will be used to develop treatment protocols, which may guide physicians on off-label prescription of biologics and may help payers to make informed decisions about reimbursement.
Off-label prescription of drugs is both legal and common and may give early access to new valuable treatments for patients, thereby adding to the innovation of clinical practice. This is especially the case in “orphan diseases” such as rare IMIDs, in which it is very difficult to conduct RCTs, but it also holds true for more common diseases as exemplified by infliximab (anti-TNF) treatment for refractory sarcoidosis. However, it is crucially important to consequently monitor efficacy and safety. We therefore advocate the use of registries, which will result in the collection of unbiased data that can be used to develop treatment guidelines for off-label prescription of biologics in individual rare IMIDs. Ultimately, this will lead to a more evidence-based and rational use of biologics in these diseases.
AM and AA performed the literature search and wrote the manuscript. AM and AA contributed equally to this paper. DG and PT treated the patient, reviewed, and edited the manuscript. ST wrote and edited the paper.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
1. Baeten D, van Hagen PM. Use of TNF blockers and other targeted therapies in rare refractory immune-mediated inflammatory diseases: evidence-based or rational? Ann Rheum Dis (2010) 69:2067–73. doi: 10.1136/ard.2009.126813
4. Chronowski GM, Ha CS, Wilder RB, Cabanillas F, Manning J, Cox JD. Treatment of unicentric and multicentric Castleman disease and the role of radiotherapy. Cancer (2001) 92:670–6. doi:10.1002/1097-0142(20010801)92:3<670::AID-CNCR1369>3.0.CO;2-Q
5. Soulier BJ, Grollet L, Oksenhendler E, Cacoub P, Cazals-Hatem D, Babinet P, et al. Kaposi’s sarcoma-associated herpesvirus-like DNA sequences in multicentric Castleman’s disease. Blood (1995) 4:1276–80.
8. De Marchi G, De Vita S, Fabris M, Scott CA, Ferraccioli G. Systemic connective tissue disease complicated by Castleman’s disease: report of a case and review of the literature. Haematologica (2004) 89:6–10.
9. Ocio EM, Sanchez-Guijo FM, Diez-Campelo M, Castilla C, Blanco OJ, Caballero D, et al. Efficacy of rituximab in an aggressive form of multicentric Castleman disease associated with immune phenomena. Am J Hematol (2005) 78:302–5. doi:10.1002/ajh.20283
10. Bower M, Veraitch O, Szydlo R, Charles P, Kelleher P, Gazzard B, et al. Cytokine changes during rituximab therapy in HIV-associated multicentric Castleman disease. Blood (2009) 113:4521–4. doi:10.1182/blood-2008-12-197053
11. Kikuchi J, Hashizume M, Kaneko Y, Yoshimoto K, Nishina N, Takeuchi T, et al. Peripheral blood CD4 + CD25 + CD127 low regulatory T cells are significantly increased by tocilizumab treatment in patients with rheumatoid arthritis: increase in regulatory T cells correlates with clinical response. Arthritis Res Ther (2015) 7:1–10. doi:10.1186/s13075-015-0526-4
12. Bayry J, Sibéril S, Triebel F, Tough DF, Kaveri SV. Rescuing CD4 + CD25 + regulatory T-cell functions in rheumatoid arthritis by cytokine-targeted monoclonal antibody therapy. Drug Discov Today (2007) 12:548–52. doi:10.1016/j.drudis.2007.05.002
13. Nishimoto N, Kanakura Y, Aozasa K, Johkoh T, Nakamura M, Nakano S, et al. Humanized anti-interleukin-6 receptor antibody treatment of multicentric Castleman disease. Blood (2005) 106:2627–32. doi:10.1182/blood-2004-12-4602
14. Song SN, Tomosugi N, Kawabata H, Ishikawa T, Nishikawa T, Yoshizaki K. Down-regulation of hepcidin resulting from long-term treatment with an anti-IL-6 receptor antibody (tocilizumab) improves anemia of inflammation in multicentric Castleman disease. Blood (2010) 116:3627–34. doi:10.1182/blood-2010-03-271791
15. Nemeth E, Tuttle MS, Powelson J, Vaughn MB, Donovan A, McVey Ward D, et al. Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization. Science (2004) 306:2090–3. doi:10.1126/science.1104742
16. Smolen JS, Schoels MM, Nishimoto N, Breedveld FC, Burmester GR, Dougados M, et al. Consensus statement on blocking the effects of interleukin-6 and in particular by interleukin-6 receptor inhibition in rheumatoid arthritis and other inflammatory conditions. Ann Rheum Dis (2013) 72:482–92. doi:10.1136/annrheumdis-2012-202469
17. Ramos-Casals M, Brito-Zerón P, Muñoz S, Soto M-J. A systematic review of the off-label use of biological therapies in systemic autoimmune diseases. Medicine (Baltimore). (2008) 87:345–64. doi:10.1097/MD.0b013e318190f170
Keywords: giant lymph node hyperplasia, multicentric Castleman’s disease, off-label use, interleukin-6, tocilizumab, biological products, registries
Citation: Musters A, Assaf A, Gerlag DM, Tak PP and Tas SW (2015) Discovery of Innovative Therapies for Rare Immune-Mediated Inflammatory Diseases via Off-Label Prescription of Biologics: The Case of IL-6 Receptor Blockade in Castleman’s Disease. Front. Immunol. 6:625. doi: 10.3389/fimmu.2015.00625
Received: 02 October 2015; Accepted: 30 November 2015;
Published: 11 December 2015
Edited by:Azzam Maghazachi, D&A Immunology and Oncology International, USA
Reviewed by:Jagadeesh Bayry, Institut National de la Santé et de la Recherche Médicale, France
Vijay Panchanathan, Perdana University Graduate School of Medicine, Malaysia
Copyright: © 2015 Musters, Assaf, Gerlag, Tak and Tas. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Anne Musters, firstname.lastname@example.org
†Present address: Paul P. Tak, GlaxoSmithKline, Stevenage, UK; University of Cambridge, Cambridge, UK