Clinical Trial: Pilot Study of Imatinib Mesylate to Treat Nephrogenic Systemic Fibrosis

Study Status: Completed
Recruit Status: Completed
Study Type: Interventional

Official Title: An Open Label Phase 2 Pilot Study to Determine the Safety, Efficacy and Tolerability of Gleevec (Imatinib Mesylate) in the Treatment of Nephrogenic Systemic Fibrosis

Brief Summary: The purpose of this study is to determine the efficacy of imatinib mesylate in reducing cutaneous thickening and tethering in patients with nephrogenic systemic fibrosis (NSF). The study will also work to assess the safety and tolerability of imatinib mesylate in patients with chronic kidney disease and NSF.

Detailed Summary:

Nephrogenic systemic fibrosis (NSF) is a recently described, extremely debilitating and painful condition that affects individuals with renal failure. Recent reports suggest an association between gadolinium exposure during magnetic resonance (MR) studies and the subsequent development of NSF in patients with chronic renal failure. NSF is characterized by rapidly progressive skin hardening, tethering and hyperpigmentation, predominantly on the extremities. Visceral involvement is rare. Skin biopsies of early NSF lesions demonstrate thickened collagen bundles, mucin deposition, angiogenesis and numerous dermal spindle cells that stain with antibodies to cluster of differentiation 34 (CD34) and procollagen. Cutaneous changes of NSF are present in up to 13% of individuals receiving hemodialysis. Among those patients with clinical evidence of NSF, the principle investigator of this protocol has recently reported that NSF is associated with increased early mortality at 24-months.

There is no proven therapy for this devastating disorder. Anecdotal reports have shown modest improvement in joint mobility and decreased skin thickening with extracorporeal photopheresis and pentoxyphylline.

Increased transforming growth factor (TGF)-beta1 messenger ribonucleic acid (mRNA) on immunostaining has been observed in skin, fascia and striated muscle. Imatinib mesylate, a tyrosine kinase inhibitor, prevents TGF-beta-induced stimulation of collagen and extracellular matrix protein synthesis as well as mRNA expression by normal fibroblasts. This observation led the principal investigator to evaluate imatinib mesylate 400 milligrams (mg) orally (p.o.) daily for 1 year in two participants with NSF. The result was significant softening of previously hardened skin with increased mobility of skin that previously had been tethered to the underlying
Sponsor: Massachusetts General Hospital

Current Primary Outcome: Percentage Change From Baseline in the Modified Rodnan Skin Score (mRSS) to Assess Skin Tethering [ Time Frame: Baseline and Month 4 ]

The modified Rodnan Skin Score is the accepted clinical measure of scleroderma skin activity. The investigator assessed the thickening of the skin using the modified Rodnan Skin Score through simple palpation on 17 different skin sites in the fingers, hands, forearms, arms, feet, legs, and thighs (bilaterally) and face, chest, and abdomen (singly). Skin thickness was assessed on a scale of 0 to 3; 0 representing normal skin and 3 being severe thickening. The sum of the individual scores can range from 0 (normal) to 51 (severe thickening in all 17 areas). Percentage change is calculated as the Month 4 Score - Baseline Score/Baseline Score * 100. A negative percentage change indicates improvement.


Original Primary Outcome: Change in modified Rodnan skin score (mRSS) to assess skin tethering [ Time Frame: 4 months ]

Current Secondary Outcome:

  • Change From Baseline in Maximal Extension of Elbows and Knees [ Time Frame: Baseline and Month 4 ]
  • Change From Baseline in Histologic Appearance of Skin Biopsy [ Time Frame: Baseline and Month 4 ]
  • Change From Baseline in Visual Analog Scale (VAS) for Pain [ Time Frame: Baseline and Month 4 ]
  • Change From Baseline in Health Assessment Questionnaire (HAQ) Score [ Time Frame: Baseline and Month 4 ]
  • Change From Baseline in Short Form 36 (SF-36) Score [ Time Frame: Baseline and Month 4 ]


Original Secondary Outcome:

  • Change in maximal extension of elbows and knees [ Time Frame: 4 months ]
  • Change in histologic appearance of skin biopsy [ Time Frame: 4 months ]
  • Change in visual analog scale (VAS) for pain [ Time Frame: 4 months ]
  • Change in health assessment questionnaire (HAQ) score [ Time Frame: 4 months ]
  • Change in SF-36 score [ Time Frame: 4 months ]


Information By: Massachusetts General Hospital

Dates:
Date Received: May 8, 2008
Date Started: December 2007
Date Completion:
Last Updated: April 10, 2017
Last Verified: April 2017