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Pilot Study of Imatinib Mesylate to Treat Nephrogenic Systemic Fibrosis

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
HaliImekamilika
Wadhamini
Massachusetts General Hospital
Washirika
Novartis Pharmaceuticals

Maneno muhimu

Kikemikali

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.

Maelezo

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.

Tarehe

Imethibitishwa Mwisho: 03/31/2017
Iliyowasilishwa Kwanza: 05/07/2008
Uandikishaji uliokadiriwa Uliwasilishwa: 05/11/2008
Iliyotumwa Kwanza: 05/12/2008
Sasisho la Mwisho Liliwasilishwa: 04/09/2017
Sasisho la Mwisho Lilichapishwa: 05/18/2017
Tarehe ya matokeo ya kwanza yaliyowasilishwa: 04/09/2017
Tarehe ya matokeo ya kwanza ya QC yaliyowasilishwa: 04/09/2017
Tarehe ya matokeo ya kwanza kuchapishwa: 05/18/2017
Tarehe halisi ya kuanza kwa masomo: 11/30/2007
Tarehe ya Kukamilisha Msingi iliyokadiriwa: 06/30/2009
Tarehe ya Kukamilisha Utafiti: 06/30/2009

Hali au ugonjwa

Nephrogenic Systemic Fibrosis

Uingiliaji / matibabu

Drug: Imatinib Mesylate (IM) Treatment

Awamu

Awamu 2

Vikundi vya Arm

MkonoUingiliaji / matibabu
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.

Vigezo vya Kustahiki

Zama zinazostahiki Kujifunza 18 Years Kwa 18 Years
Jinsia Inastahiki KujifunzaAll
Hupokea Wajitolea wa AfyaNdio
Vigezo

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

Matokeo

Hatua za Matokeo ya Msingi

1. Percentage Change From Baseline in the Modified Rodnan Skin Score (mRSS) to Assess Skin Tethering [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.

Hatua za Matokeo ya Sekondari

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]

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