Pilot Study of Imatinib Mesylate to Treat Nephrogenic Systemic Fibrosis
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Mücərrəd
Təsvir
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 fascia. After one month of imatinib mesylate, one of the two participants had a 20 degree reduction of his knee flexion contractures.
Tarixlər
Son Doğrulandı: | 03/31/2017 |
İlk təqdim: | 05/07/2008 |
Təxmini qeydiyyat təqdim edildi: | 05/11/2008 |
İlk Göndərmə: | 05/12/2008 |
Son Yeniləmə Göndərildi: | 04/09/2017 |
Son Yeniləmə Göndərildi: | 05/18/2017 |
İlk təqdim edilmiş nəticələrin tarixi: | 04/09/2017 |
İlk təqdim edilmiş QC nəticələrinin tarixi: | 04/09/2017 |
İlk göndərilən nəticələrin tarixi: | 05/18/2017 |
Həqiqi Təhsilin Başlama Tarixi: | 11/30/2007 |
Təxmini İlkin Tamamlanma Tarixi: | 06/30/2009 |
Təxmini İşin Tamamlanma Tarixi: | 06/30/2009 |
Vəziyyət və ya xəstəlik
Müdaxilə / müalicə
Drug: Imatinib Mesylate (IM) Treatment
Faza
Qol Qrupları
Qol | Müdaxilə / müalicə |
---|---|
Experimental: Imatinib Mesylate (IM) Treatment Imatinib mesylate 400 milligrams (mg) orally once daily for 4 months. Dosage was reduced to 200 mg if the participant developed gastrointestinal intolerance or alopecia. | Drug: Imatinib Mesylate (IM) Treatment 400 mg p.o. daily for 4 months. Dosage was reduced to 200 mg if participants develop gastrointestinal intolerance or alopecia. |
Uyğunluq Kriteriyaları
Təhsil üçün uyğun yaşlar | 18 Years Üçün 18 Years |
Təhsilə Uyğun Cinslər | All |
Sağlam Könüllüləri qəbul edir | Bəli |
Kriteriyalar | Inclusion Criteria: - Age > 18 years - Biopsy-proven NSF - Ability to give consent Exclusion Criteria: - Known sensitivity to imatinib mesylate or to any of its components - Pregnant or lactating woman - Bullous dermatologic disease - Aspartate aminotransferase / alanine aminotransferase (AST/ALT) >3 x upper limit of normal - Severe congestive heart failure [New York Heart Association (NYHA) Class III or IV] - Patients who have received Gleevec in the past 12 months |
Nəticə
İlkin nəticə tədbirləri
1. Percentage Change From Baseline in the Modified Rodnan Skin Score (mRSS) to Assess Skin Tethering [Baseline and Month 4]
İkincili Nəticə Tədbirləri
1. Change From Baseline in Maximal Extension of Elbows and Knees [Baseline and Month 4]
2. Change From Baseline in Histologic Appearance of Skin Biopsy [Baseline and Month 4]
3. Change From Baseline in Visual Analog Scale (VAS) for Pain [Baseline and Month 4]
4. Change From Baseline in Health Assessment Questionnaire (HAQ) Score [Baseline and Month 4]
5. Change From Baseline in Short Form 36 (SF-36) Score [Baseline and Month 4]