Drug Therapy of Lupus

This site is intended for healthcare professionals as a useful source of information on the diagnosis, treatment and support of patients with lupus and related connective tissue diseases.

Introduction

It would be wrong to sugest that the management of lupus is easy. The disease has numerous manifestations and each person has their own pattern of disease which can change over time, sometimes rapidly. In general, patients who present with severe lupus e.g. of the kidneys or central nervous system (CNS), and those with multiple autoantibodies tend to have persistent serious disease. Patients who present with mild disease may continue to have mild disease but, as time goes by, many will develop more serious manifestations, so it is important to consider whether any new symptom might represent a new manifestation of the disease.

Treatment of specific disease manifestations is dealt with in the relevant chapters of this book so an overview of the drug management is given here. Treatment depends upon clinical assessment of the extent of organ involvement and also of its severity (Table 1).

Assessment of disease activity

Investigations are dealt with in detail elsewhere, however, clinical assessment of disease activity is as important as the results of laboratory tests. Tiredness, fever or mood disturbance can indicate a flare of disease, as well as more obvious manifestations such as rash or arthritis. Where there is significant internal organ involvement then appropriate tests can be used to monitor disease activity e.g. serum creatinine, eGFR, urinary protein or lung function tests. Otherwise, it is often possible to identify a test which reflects disease activity in an individual patient. This may be the DNA binding level, the serum C4 or C3 concentration, the white cell count, haemoglobin or, perhaps, even the ESR. Such combined clinical and laboratory assessment helps one to decide whether it is necessary to use more aggressive treatment or, alternatively, whether the dose of medication can be reduced.

Various disease assessment indices have been developed e.g. BILAG, SLEDAI, SLAM & ECLAM and are used in specialist units. They variably assess disease activity and tissue damage and it can be difficult to distinguish the effects of currently active inflammation from those of established damage. Quality of life may also be assessed by measures such as the SF-36 questionnaire.

It is reasonable to divide lupus into mild, intermediate or severe disease, although even in mild disease symptoms such as malaise or arthralgia can be very disabling. The main therapeutic agents are shown in Table 2, although other drugs may be used in specific circumstances and are discussed in the relevant chapters. The management of clotting problems associated with anti-phospholipid antibodies and of lupus in pregnancy are fully discussed elsewhere in this book.

Mild disease

Common manifestations are arthralgia, rashes, photosensitivity, mouth ulcers, Raynaud’s phenomenon, hair loss and fatigue.Often symptoms can be reasonably controlled by analgesics and measures to reduce sun exposure, including the use of high factor sunscreens. Hydroxychloroquine is often useful in this type of disease. Mepacrine can be a useful alternative to hydroxychloroquine or used in combination with it when the response is inadequate.

Fatigue may be disabling despite control of other symptoms and may occasionally justify a trial of low dose steroid e.g. prednisolone 5-7.5mg daily, although results are often disappointing. Arthritis or rashes may respond to such doses but higher doses of steroid should generally be avoided in this type of disease since the risk of toxicty is likely to outweigh benefits. It is important to consider alternative explanations for fatigue such as anaemia, depression, a side-effect of medication or hypothyroidism, which is more common in people with lupus than in the general population. A healthy diet and regular gentle exercise should be encouraged.

NSAIDs are also reasonably effective for symptom control but should be used with caution in lupus as they often cause an increase in blood pressure, fluid retention and can impair renal function. Furthermore, it now seems clear that both conventional NSAIDs (apart, perhaps, from naproxen) and the newer COX-2 selective NSAIDs can cause a modest increase in the risk of heart attack and stroke. As the risk of cardiovascular disease is increased in lupus, any additional risk is to be avoided. They can also impair ovulation and, if used during pregnancy beyond the 20th week, can constrict the ductus arteriosus and impair foetal renal function.

Intermediate disease

This category includes those with pleurisy, pericarditis, severe rashes and haematological manifestations such as thrombocytopenia and leucopenia. In such cases steroids are usually required. The aim is to use a dose sufficient to control the disease and then reduce it to as low a maintenance dose as possible. It is difficult to generalise regarding dose. Pleurisy can usually be controlled by about 20mg prednisolone daily, whereas, haematological problems may require doses of 40mg or more for disease suppression.

Hydroxychloroquine may be adequate in conjunction with steroids but often immunosuppression is required. Azathioprine has been used most widely but in recent years methotrexate has been used increasingly as has mycophenolate. Cyclosporin can also be useful, particularly in the treatment of thrombocytopenia, but because of its tendency to cause hypertension and to impair renal function it has to be used with great care in lupus. All of these drugs take some time to take effect, e.g. 1-3 months, and during this period steroids will be required in a dose sufficient to control the disease.Once the patient is stabilised on the immunosuppressive drug every effort should be made to reduce the dose of steroid to the lowest at which disease control can be maintained.

Severe disease

Significant renal, CNS and severe skin or haematological disease fall into this category. The different sub-types and their distinct prognoses and treatments are discussed in more detail in the relevant chapters. In CNS disease, cerebral lupus has to be distinguished from clotting problems associated with antiphospholipid antibodies, as anticoagulation rather than immunosuppression will be required for the latter. Steroids will almost inevitably be required plus an immunosuppressive drug. Predisolone 1-2mg/kg or pulsed intravenous methylprednisolone may be needed to bring the disease under control. Hydroxychloroquine is rarely adequate in this type of disease. Azathioprine, methotrexate or mycophenolate may be useful for their immunosuppressive and steroid-sparing effects. Treatment can be divided into an initial induction phase in which active disease is brought under control, followed by a maintenance phase of less intensive therapy designed to keep it under control.

Cyclophosphamide has been the mainstay of treatment for severe manifestations of lupus since the landmark NIH trials of the 1980s, especially for bad renal or CNS disease or pneumonitis.This can be given either as intermittent intravenous bolus infusions or taken daily by mouth. The dose and frequency used will depend upon the severity of disease e.g. acute cerebral vasculitis may require weekly intravenous cyclophosphamide plus pulsed intravenous steroid whereas subacute disease such as deteriorating renal function may respond to monthly intravenous or oral cyclophosphamide plus oral steroids. Mycophenolate is proving to be a less toxic and useful alternative to cyclophosphamide and has supplanted it in moderately severe cases, although cyclophosphamide may still have a place in the induction phase of treatment in very severe disease. If cyclophosphamide is used one generally tries to transfer to mycophenolate, azathioprine or methotrexate for maintenance treatment as soon as possible.

Additional treatments used in severe lupus include intravenous immunoglobulin, plasma exchange and monoclonal antibodies. Intravenous immunoglobulin is widely used for thrombocytopenia but can be helpful for other manifestations. Plasma exchange is used less frequently now than in the past but many still believe that it can be helpful in acute, severe disease, particularly cerebral lupus. Monoclonal antibodies, particularly rituximab, are extremely promising and are likely to play a major part in the management of severe and intermediate disease.

Co-morbidity

It has become clear in recent years that lupus is a major risk factor for the development of cardiovascular disease and that myocardial infarction and stroke are much more common in people with lupus than in the general population. As well as conventional risk factors such as hypertension, hyperlipidaemia, smoking and obesity, other factors are involved. These include antiphospholipid antibodies; endothelial dysfunction and lipid peroxidation in the vessel wall; use of NSAIDs and HRT, and steroid-induced diabetes. As well as seeking optimal control of the disease, it is imperative to check blood pressure and fasting lipids and glucose regularly, to institute appropriate treatment where necessary and to strongly discourage smoking in order to minimise cardiovascular risk factors.

Comments on individual drugs

Steroids

The correct use of steroids is key to the management of lupus.The disease may be under-treated but a more common mistake is to continue high dose steroids for too long. Mild disease may respond to 5-10mg prednisolone daily. For more severe disease 20-40mg may be required and for severe disease 1mg/kg or more or the use of pulsed intravenous methylprednisolone. Every effort should be made to taper the dose to the lowest sufficient to maintain disease control. In patients who have had severe disease there is often a flare-up when the daily prednisolone dose is reduced to between 7.5 and 15mg daily. This should be borne in mind when monitoring someone with lupus and it is often wise to reduce the prednisolone by 1mg at a time when the daily dose is below 15mg.

Steroid-induced osteoporosis is a common problem in people with lupus. National guidelines recommend that anyone who receives more than 7.5mg prednisolone daily for three months and is aged 65+ or has had a previous fragility fracture should receive osteoprotective treatment. Younger people should have their bone density measured serially by DEXA scan. We now have effective osteoprotective agents in the form of bisphosphonates (Fosamax, Actonel, Bonviva) and strontium ranelate (Protelos). HRT is no longer used for the prevention or treatment of osteoporosis because of the increased risk of breast cancer and cardiovascular disease. Although Raloxifene (Evista) reduces the risk of breast cancer it increases the risk of venous thromboembolism and has not been shown to reduce the frequency of non-vertebral fractures, so it is a poor alternative to bisphosphonates and strontium ranelate. It is not known whether treatment of women of child-bearing age with bisphosphonates poses any hazard to children born subsequently. Bisphposphonates are contra-indicated during pregnancy and it is recommended that pregnancy should be postponed for six months after withdrawal of bisphosphonates.

Increased susceptibility to infection is another major concern, especially in those who are also on immunosuppressive drugs. Steroids may aggravate hypertension, provoke diabetes and have an adverse effect on lipid profile which probably contributes to the increased cardiovascular mortality in lupus. In high doses steroids increase the risk of gastrointestinal bleeding and will do so at lower doses when taken with NSAIDs. Osteonecrosis (avascular necrosis) is also fairly common in lupus and seems to be associated particularly with the use of highdose oral steroids or pulsed intravenous methylprednisolone.

Antimalarials

Hydroxychloroquine (Plaquenil) is generally preferred to chloroquine because the risk of ocular toxicity is believed to be greater with the latter. Ocular toxicity is related both to the daily and cumulative dose and the daily dose should not exceed 6.5mg/kg lean body weight. So long as this dose is not exceeded the risk of eye problems is very small. The manufacturers recommend a baseline ophthalmological check and annual review, however, the Royal College of Ophthalmologists has recommended that patients should have baseline and annual visual acuity checks performed by the prescribing doctor and be referred to an ophthalmologist only if a visual problem is identified at baseline or reduced acuity or blurred vision develop on treatment. Hydroxychloroquine has the benefits of reducing cholesterol levels, a modest anti-platelet effect and it may reduce the extent of permanent tissue injury in lupus. Hydroxychloroquine appears to be safe in pregnancy.

The addition of mepacrine 50-100mg daily may be useful in those not responding to hydroxychloroquine alone. Mepacrine is not thought to be associated with ocular side-effects.

Azathioprine

Azathioprine (Imuran) is an immunosuppressant antimetabolite: it reduces purine biosynthesis which is necessary for proliferation of cells including those of the immune system. It is generally used in a dose of 1-2.5mg/kg. Nausea is common while leucopenia and thrombocytopenia occur in some 4% of cases. Monitoring the drug can be a problem if people with lupus already have such clinical features. Abnormal liver function tests occur in a similar proportion of people. Azathiorpine is catabolised by the enzyme thiopurine methyltransferase (TPMT) and about 1 in 300 people have a deficient genetic polymorphism of TPMT which renders them susceptible to severe drug toxicity. Laboratory testing can identify people at risk and so protect them from exposure to the drug, access to such testing is becoming more available in the NHS.Azathioprine is considered safe to use during pregnancy in doses up to 2mg/kg.

Mycophenolate mofetil

Mycophenolate mofetil (CellCept) inhibits purine synthesis, lymphocyte proliferation and T cell-dependent antibody responses. Compared with cyclophosphamide it does not cause ovarian failure and is less likely to be associated with serious infection, leucopenia or severe alopecia. It is also probably more effective and better tolerated than azathioprine. It has rapidly assumed a central role in the management of lupus. It is contra-indicated in pregnancy and should only be used in women of child-bearing age in conjunction with reliable contraception. Because of its long half-life it should be stopped at least six weeks before planned conception.

Methotrexate

Methotrexate (Maxtrex) is a folic acid antagonist and is classified as an antimetabolite cytotoxic agent; it has many effects on cells of the immune system including modulation of cytokine production. It is used in a once weekly regimen typically starting at a dose of 7.5mg per week building up to 20mg weekly if required. Folic acid 5-10mg once weekly (not on the same day as the methotrexate) is routinely given to reduce the risk of side-effects. Nausea and mouth ulcers are fairly common and leucopenia, thrombocytopenia and abnormal liver function tests occur occasionally. Methotrexate is contra-indicated during pregnancy and should be used in women of child-bearing age only in conjunction with effective contraception.The drug should be withdrawn three months before conception is attempted.

Cyclosporin

Cyclosporin (Neoral) inhibits the action of calcineurin and so leads to reduced function of effector T lymphocytes. It is used in a dose of 2.5-5mg/kg daily. Hypertension and an increase in serum creatinine are common and this makes it difficult to use in lupus where such features are often already present. Careful monitoring of blood pressure and creatinine are essential. It is considered reasonable to use it during pregnancy at the lowest effective dose with careful attention to blood pressure and renal function.

Cyclophosphamide

This is an alkylating anti-neoplastic agent. It has been used extensively for the treatment of patients with lupus and internal organ involvement over the past four decades. It has been shown to improve the outcome of renal disease to a greater extent than steroids alone and is still widely used for the treatment of severe CNS, renal or pulmonary disease. It can be given in a daily oral dose of 0.5-2mg/kg, or as intravenous infusions. The dose and frequency of intravenous infusions vary according to disease severity, but doses of 7.5-15mg/kg every four weeks are often used.

The main hazards are increased risk of infection; ovarian failure; bladder toxicity, and increased risk of subsequent malignancy. The risk of haemorrhagic cystitis can be reduced somewhat by giving MESNA concurrently. It is teratogenic and impairs gonadal function in both men and women. Ovarian failure is closely related to the dose given and also the age of the patient: over 25 the risk increases significantly. In young people who want children subsequently storage of sperm or ovarian harvest and storage of eggs should be considered.The drug should be withdrawn three months before conception is attempted.

Intravenous immunoglobulin

This is a recognised treatment for thrombocytopenic purpura and can be helpful for other manifestations of lupus. The mode of action is unclear but saturation of Fc receptors and alteration of the idiotypic network are possible mechanisms. It is usually given in a dose of about 0.5g/kg as an intravenous infusion on three consecutive days and repeated at intervals depending on response. It can be used safely during pregnancy.

Rituximab

Rituximab (Mabthera) is a monoclonal antibody which reacts with the CD20 molecule on mature B cells and pre-B cells. CD20 is not, however, expressed on B cell progenitors or plasma cells, which means that the humoral immune system is not switched off completely. In early studies it was given in combination with cyclophosphamide but now it is often given with methotrexate. Following infusion of rituximab there is a sustained decrease in circulating B cells for several months but only a modest reduction in total immunoglobulin levels. Autoantibody levels tend to fall more than other antibodies. Rituximab has led to dramatic improvement in some people with refractory lupus and a repeat course of treatment has been effective in some of those who relapsed. This agent is being studied in people with earlier disease and clearly represents a major therapeutic advance. Epratuximab, a monoclonal antibody which reacts with another B cell antigen (CD22), is also showing considerable promise.

Other agents

In certain circumstances, other drugs may be needed to control specific disease manifestations, or when more commonly used drugs prove ineffective or are not tolerated. These include mepacrine, leflunomide, dapsone, thalidomide, quinacrine and clofazimine. These are discussed elsewhere in this book. A number of monoclonal antibodies and other biological agents which affect cells of the immune system or inhibit cytokines are being studied and it is very likely that additional agents will become available for treatment within the next few years.

Conclusion

The management of lupus requires careful disease monitoring and interpretation of laboratory results and judicious use of the available drugs. It involves a constant struggle to strike the correct balance between under-treatment and overtreatment of the disease. Patients are often well informed about their disease and should be viewed as partners in disease management. Close collaboration between GP and specialist is essential for optimal disease management.


Table 1 - Questions to ask in the management of Lupus


What are the disease manifestations?
How active is the disease?
How am I monitoring the disease?
Am I treating the disease vigorously enough?
Am I over-treating the disease at present?
Do I need to involve a colleague?

Remember:

Check the blood pressure & renal function regularly
Check the urine for protein regularly
Check fasting lipids & glucose periodically
If uncertain about blood results, disease activity or its management do not hesitate to discuss with a specialist
Table 2. Side-effects of drugs and important interactions*




Azathioprine




Cyclosporin





Cyclophosphamide



Hydroxychloroquine



Methotrexate




Mycophenolate
Very common
(greater than)10%


Leucopenia


Hypertension
Renal dysfunction
Tremor
Headache
Hyperlipidaemia

Leucopenia
Azospermia
Ovarian failure
Alopecia
Mouth ulcers





Nausea


Infection
Leucopenia
Thrombocytopenia
Nausea
Diarrhoea
Common
1-10%


Thrombocytopenia


Nausea
Gingival hyperplasia
Myalgia
Hypertrichosis
Paraesthesia
Hyperuricaemia

Haemorrhagis cystitis
Hyponatraemia


Nausea
Rash
Mouth ulcers

Leucopenia
Hepatic dysfunction
Diarrhoea

Hyperlipidaemia
Headache
Rash
Hepatic & renal dysfunction
Uncommon
0.1 - 1%


Infections
Anaemia
Pancreatitis


Anaemia
Thrombocytopenia



Tumours




Retinopathy



Pneumonitis



Skin cancer
Important
interactions



Allopurinol

Carbamazepine
Phenytoin
Erythromycin
Diltiazem
St John’s wort
Grapefruit juice

Oral hypoglycaemic drugs




Digoxin


Trimethoprim
Cotrimoxazole
Acitretin


Colestyramine
* Monitoring guidelines can be found on the British Society for Rheumatology website at www.rheumatology.org.uk

Dr Robin Butler
Consultant Rheumatologist
Leopold Muller Arthritis Research Centre
Robert Jones & Agnes Hunt Orthopaedic Hospital
Oswestry
Shropshire SY10 7AG