Literature DB >> 12817067

Current therapeutic possibilities in primary and secondary amyloidosis and our experience with 31 patients.

R Rysavá1, M Merta, I Spicka, V Tesar.   

Abstract

Primary (AL) and secondary (AA) amyloidosis are systemic diseases characterized by a process of amyloid deposition in many organs with unsatisfactory survival of patients. Apart from surgical intervention in those patients with bronchiectasias or osteomyelitis, the possibilities of influencing the development of AA amyloidosis are limited. The milestone therapy in patients with rheumatic diseases includes early treatment with DMARDs (disease-modifying antirheumatic drugs). A new promising therapeutic alternative is represented by anti-tumour necrosis factor-alpha (TNF-alpha) drugs such as infliximab and etanercept. The last class of agents used in the treatment of AA interferes with fibril formation: iododoxorubicin and low molecular weight sulfates (fibrilex). In the group of patients with AL, in addition to the standard combination of melphalan and prednisone, other therapeutic approaches such as ASCT (autologous stem cell transplantation) and new drugs with different mechanisms of action have been added recently. For the future, we can expect the development of immunotherapy (both active vaccination and passive immunization). In our department, we have treated 17 patients with AL and 14 patients with AA amyloidosis since 1995. We used various treatment regimens in both groups of patients. The treatment stabilized the disease or achieved partial remission in only 36% of patients with AA amyloidosis despite the use of intensive therapeutic modalities, while in the AL group a response was achieved in 82% of patients. ASCT improves patients survival in AL amyloidosis, but strict selection criteria are necessary (less than two affected organs and no signs of myocardial dysfunction).

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Year:  2003        PMID: 12817067     DOI: 10.1093/ndt/gfg1043

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  4 in total

1.  Secondary amyloidosis in Crohn's disease: treatment with tumour necrosis factor inhibitor.

Authors:  M M Boscá; C M Pérez-Baylach; M A Solis; R Antón; E Mayordomo; S Pons; M Mínguez; A Benages
Journal:  Gut       Date:  2006-02       Impact factor: 23.059

2.  Renal AA amyloidosis: survey of epidemiologic and laboratory data from one nephrology centre.

Authors:  Z Potysová; M Merta; V Tesar; E Jancová; E Honsová; R Rysavá
Journal:  Int Urol Nephrol       Date:  2009-01-31       Impact factor: 2.370

Review 3.  New advances in renal amyloidosis.

Authors:  Shinichi Nishi; Bassam Alchi; Nofumi Imai; Fumitake Gejyo
Journal:  Clin Exp Nephrol       Date:  2008-01-05       Impact factor: 2.801

Review 4.  Renal amyloidosis in children.

Authors:  Yelda Bilginer; Tekin Akpolat; Seza Ozen
Journal:  Pediatr Nephrol       Date:  2011-03-01       Impact factor: 3.714

  4 in total

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