What is the next best treatment option for a patient with dermatomyositis and scleroderma features, presenting with inflammatory polyarthritis, currently on Rituximab (Rituxan), Plaquenil (Hydroxychloroquine), and Cellcept (Mycophenolate mofetil)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: April 11, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

From the Guidelines

For dermatomyositis with scleroderma features and persistent inflammatory polyarthritis despite current therapy with rituximab, plaquenil, and CellCept, the next best treatment option would be adding methotrexate, as it has shown promise in treating skin involvement in systemic sclerosis, with a between-group difference of approximately 5 points in mRSS in favor of methotrexate, compared with placebo 1. Methotrexate is typically administered as 15-25 mg per week, and its effectiveness in treating inflammatory polyarthritis is well-established. Key considerations for treatment include:

  • Monitoring for potential side effects, such as liver toxicity and bone marrow suppression
  • Regular blood work every 4-8 weeks to monitor complete blood count, liver function, and kidney function
  • Screening for tuberculosis, hepatitis B and C, and updating vaccinations before initiating methotrexate Other viable options, such as cyclophosphamide, tocilizumab, or rituximab, may also be considered, but methotrexate is a more commonly used first-line treatment for skin manifestations in patients with dcSSc 1. It is essential to weigh the benefits and risks of each treatment option and consider the individual patient's needs and medical history when making a decision. In general, treatment should be aimed at reaching a target of sustained remission or low disease activity, and monitoring should be frequent in active disease, with adjustments to therapy as needed 1.

From the Research

Treatment Options for Dermatomyositis with Scleroderma Features

The patient is currently experiencing inflammatory polyarthritis, and is being treated with rituximab, plaquenil, and Cellcept. Considering the current treatment regimen, the next best option for treatment could be:

  • Adding a steroid-sparing immunosuppressive agent, such as methotrexate or azathioprine, to reduce the dose of glucocorticoids and minimize their adverse effects 2, 3
  • Using biologics, such as abatacept, which has shown promise in treating inflammatory myopathies 3
  • Considering multi-target treatment with glucocorticoids and several steroid-sparing immunosuppressive agents, which has been effective in refractory cases 3

Management of Inflammatory Polyarthritis

For the management of inflammatory polyarthritis, the following options could be considered:

  • Adding a disease-modifying antirheumatic drug (DMARD), such as methotrexate or sulfasalazine, to the current treatment regimen 2, 3
  • Using biologics, such as rituximab, which has already been initiated, or other biologics like abatacept or tocilizumab 3
  • Considering the use of Janus kinase inhibitors, which are a new class of drugs that have shown promise in treating inflammatory arthritis 4

Monitoring and Evaluation

Regular monitoring and evaluation of the patient's condition is crucial to assess the effectiveness of the treatment and to adjust the treatment regimen as needed. This includes:

  • Regular assessment of muscle strength and inflammatory markers 2
  • Monitoring for potential internal malignancy, which is a known association with dermatomyositis 4, 5, 6
  • Evaluation for esophageal dysfunction, cardiopulmonary disease, and other systemic complications 6

References

Related Questions

What is the next best treatment option for a patient with dermatomyositis (DM) and scleroderma features, presenting with inflammatory polyarthritis?
What are the cardiovascular manifestations of dermatomyositis (inflammatory muscle disease)?
What is dermatomyositis?
What is the latency period for a dermatomyositis (DM) flare after ultraviolet (UV) exposure?
What is the treatment approach for dermatomyositis (inflammatory muscle disease) following Epstein-Barr Virus (EBV) infection?
What antibiotics are safe during pregnancy for a sebaceous cyst on the ear?
What are the aesthetic benefits of applying ice to the skin, specifically cryotherapy (cold therapy)?
What is the next best treatment option for a patient with dermatomyositis (DM) and scleroderma features, presenting with inflammatory polyarthritis?
What is the next step in managing a patient with a history of normal myocardial perfusion study, normal ejection fraction (EF) between 65-70%, mild left ventricular hypertrophy (LVH), impaired relaxation filling pattern, mild aortic valve calcification, and moderate mitral valve calcification, who presents with shortness of breath, 1+ to 2+ pitting edema, and is currently on Furosemide (Lasix) 20 milligrams (mg) daily?
Is a single dose of Diflucan (fluconazole) 150mg sufficient for treating candidiasis?
What is the next best treatment option for a patient with dermatomyositis and scleroderma overlap syndrome, presenting with inflammatory polyarthritis and skin changes, currently on rituximab (Rituxan), plaquenil (hydroxychloroquine), prednisone, Cellcept (mycophenolate mofetil), and actemra (tocilizumab), having previously tried methotrexate, xeljanz (tofacitinib), leflunomide, and sulfasalazine?

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.