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Phase 2 N=30 Treatment

Imatinib Mesylate (Gleevec) in the Treatment of Systemic Sclerosis

Systemic Sclerosis

Enrolled (actual)
30
Serious AEs
40.0%
Results posted
Feb 2018
Primary outcome: Primary: Improvement in the Modified Rodnan Skin Score — -6.6 units on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Imatinib Mesylate (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Hospital for Special Surgery, New York
Primary completion
Dec 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Improvement in the Modified Rodnan Skin Score
-6.6
SECONDARY
Improvement in Indices of Pulmonary Function Measured by Change in FVC % Predicted
6.4
SECONDARY
Improvement in Indices of Pulmonary Function Measured by Change DLCO hb Adj % Predicted
5.5
SECONDARY
Change From Baseline at Month 12 in Short Form-36 (SF-36) Questionnaire:Mental Component Summary
-6.6
SECONDARY
Scleroderma Health Assessment Questionnaire Disability Index
0.02
SECONDARY
Change From Baseline at Month 12 in Short Form-36 (SF-36) Questionnaire: Physical Component Summary
6.8

Summary

The purpose of this study is to assess the safety and tolerability of imatinib mesylate (Gleevec) in patients with systemic sclerosis (scleroderma). Gleevec is a medication already FDA approved for the treatment of chronic myelogenous leukemia (CML), gastrointestinal stromal tumors (GIST), dermatofibrosarcoma protuberans tumors, Philadelphia chromosome-positive acute lymphoblastic leukemia, hypereosinophilic syndrome, and aggressive systemic mastocytosis. In-vitro studies have suggested that imatinib may inhibit collagen production by scleroderma fibroblasts, and in mouse models of fibrosis imatinib has been shown to decrease skin thickness. This is a Phase IIa, single center, prospective open label clinical trial of Gleevec in patients with systemic sclerosis. All patients will be treated with active drug for 12 months. The primary objective of this study will be to determine the safety and tolerability of Gleevec in patients with systemic sclerosis, but important secondary outcomes of relevance will be improvement in disease status as defined by skin scores and indices of pulmonary function. Patients who complete the initial phase (described above) of the study will be eligible to participate in an extension phase. The purpose of the extension phase of the study is to give patients who participated in the phase IIa clinical trial of Gleevec at the Hospital for Special Surgery the opportunity to continue Gleevec treatment if both the treating physicians and the patient are in agreement that Gleevec had acceptable safety and tolerability, as well as possible efficacy during the initial year of therapy.

Eligibility Criteria

Inclusion Criteria

  • Age greater than or equal to eighteen years.
  • Clinical diagnosis of diffuse systemic sclerosis by ACR criteria, with a stable modified Rodnan skin score in the one month preceding introduction of oral Gleevec therapy. The modified Rodnan skin score must be greater than or equal to sixteen at screening and initiation of therapy.
  • Disease duration of less than or equal to 10 years.
  • Estimated ejection fraction of greater than 50% by echocardiography

Exclusion Criteria

  • Inability to render informed consent in accordance with institutional guidelines.
  • Disease duration of greater than 10 years.
  • Patients with mixed connective tissue disease or "overlap" (i.e. those who satisfy more than one set of ACR criteria for a rheumatic disease.)
  • Ongoing treatment with other immunosuppressive therapies including cyclophosphamide, azathioprine, mycophenolic acid, methotrexate, or cyclosporine, or use of those medications within 3 months of trial entry.
  • Concurrent serious medical condition which in the opinion of the investigator makes the patient inappropriate for this study such as uncontrollable CHF, arrhythmia, severe pulmonary or systemic hypertension, severe GI involvement, serum creatinine of greater than 2.0, active infection, severe diabetes, unstable atherosclerotic cardiovascular disease, malignancy, HIV, or severe peripheral vascular disease.
  • The use of other anti-fibrotic agents including colchicine, D-penicillamine, minocycline, or Type 1 oral Collagen in the three months prior to enrollment.
  • Limited scleroderma.
  • Systemic sclerosis-like illness associated with environmental or ingested agents such as toxic rapeseed oil, vinyl chloride, or bleomycin.
  • A positive pregnancy at entry into this study. Men and women with reproductive potential will be required to use effective means of contraception through the course of the study.
  • Use in the prior month of corticosteroids at doses exceeding the equivalent of prednisone 10 mg daily. Use of corticosteroid at < 10 mg of prednisone can continue but not be increased during the course of the study.
  • Participation in another clinical research study involving the evaluation of another investigational drug within ninety days of entry into this study.
  • The presence of severe lung disease as defined by a diffusion capacity of less than 30% of predicted.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00555581). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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