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This is a plain English summary of an original research article. The views expressed are those of the author(s) and reviewer(s) at the time of publication.

This NIHR trial found no difference in the healing of pyoderma gangrenosum over six weeks in adults treated with prednisolone or ciclosporin. Pyoderma gangrenosum is a rare serious skin condition causing painful ulcers, and over half of ulcers had failed to heal after six months of either treatment. There were more serious side effects – mostly serious infections – in patients using prednisolone, though both drugs caused some harms in two thirds of patients. With little to choose between the drugs for benefit, it may be best to select the treatment based on the features of individuals that make them prone to the different adverse effects of each drug.

Why was this study needed?

Pyoderma gangrenosum is a rare skin condition causing painful ulcers that can become infected though it is not caused by infection, indeed the cause is unknown. In the UK one to two people a year will develop the condition in a population of 200,000.

The only previous randomised controlled trial in pyoderma gangrenosum was a small study, including 30 adults, which compared a biological treatment not normally prescribed for this condition with placebo. As there is so little useful evidence, the NIHR funded this study to compare the treatment of pyoderma gangrenosum using the common steroid prednisolone, thought to have benefit but some side-effects, with ciclosporin, the immunosuppressant drug, thought by clinicians to be more effective albeit with significant but different side-effects.

What did this study do?

This randomised controlled trial, called STOP GAP, included 112 adults with pyoderma gangrenosum in the UK. They were randomised to receive, by mouth, prednisolone up to 0.75mg per kg per day (max 75mg) or ciclosporin up to 4mg per kg per day (max 400mg).

The main outcome of interest was speed of healing over six weeks. This was assessed using digital photographs of ulcer size. Assessors were unaware of the treatment given, reducing possible bias in the interpretation of the photographs. Patients and their clinicians were aware of the treatment they were taking.

What did it find?

  • There was no difference in the main outcome, speed of healing, between the two treatments over six weeks. Average reduction in ulcer size per day was 0.14 square cm using prednisolone compared with 0.21 square cm using ciclosporin but this difference became insignificant at 0.003 square cm per day, when differences in the two groups were accounted for.
  • There was no significant difference between the two groups for any of the other outcomes: time to healing (defined as when sterile dressings were no longer needed), overall treatment response, self-reported pain, quality of life, time to recurrence of ulcers and number of treatment side effects.
  • Side effects, reported by around two-thirds of participants, varied depending on the treatment. Ciclosporin was more commonly associated with kidney problems (30%), nausea (20%) and headaches (8%); prednisolone with raised blood sugar (9%) and new cases of diabetes (6%).
  • Seven serious side effects were reported with prednisolone, six of which were serious infections. Two serious side effects were reported using ciclosporin, one of which was acute kidney failure.

What does current guidance say on this issue?

There are no UK or international guidelines on treating pyoderma gangrenosum. Patient information from NHS Choices and the British Association of Dermatologists list a number of treatment options. These include: steroid creams applied directly to the ulcer, drug treatment with antibiotics, steroids such as prednisolone, or immunosuppressant drugs like ciclosporin.

What are the implications?

Prednisolone and ciclosporin both helped ulcer healing to an equal degree. But there were differences in types of side effects. Therefore, shared decisions about treatment options should be mindful of the specific possible side effects, especially if patients have other conditions making them more vulnerable to certain side effects.

Fewer than half of ulcers had healed at six weeks, suggesting that neither treatment was particularly effective in treating pyoderma gangrenosum. Because this trial did not have a placebo comparison, it is possible that neither drug affected the pyoderma gangrenosum.

Although ciclosporin is used to treat pyoderma gangrenosum in the UK, it is used “off-label”, which means that it is not currently licensed for use in this condition. The study authors note that ciclosporin is more expensive than prednisolone, but the cost of treatment was not measured in this study.

Citation

Ormerod AD, Thomas KS, Craig FE, et al. Comparison of the two most commonly used treatments for pyoderma gangrenosum: results of the STOP GAP randomised controlled trial. BMJ. 2015;350:h2958.

This project was funded by the National Institute for Health Research Programme Grants for Applied Research, project number RP-PG-0407-10177.

Bibliography

Brooklyn TN, Dunnill MG, Shetty A, et al. Infliximab for the treatment of pyoderma gangrenosum: a randomised, double blind, placebo controlled trial. Gut. 2006;55:505-9.

NHS Choices. Pyoderma gangrenosum. London: NHS Choices; updated 2015.

Produced by the University of Southampton and Bazian on behalf of NIHR through the NIHR Dissemination Centre


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The exact cause of pyoderma gangrenosum is not known. It sometimes occurs in people who have another health condition such as inflammatory bowel disease, rheumatoid arthritis and some forms of blood cancer. It can also occur in people who have had surgery or other trauma to the skin. However, in around half of people, there is no obvious cause.

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