Key result
Anti-plasma cell therapies and autologous stem cell transplantation improve clinical prognosis in cardiac amyloidosis.
Why the study?
To identify emerging therapeutic options and the most effective treatments for patients with cardiac amyloidosis, assess their clinical characteristics, and discuss their impact on disease progression and quality of life.
Do emerging therapeutic options reduce disease progression and improve quality of life in patients with cardiac amyloidosis?
Do emerging therapeutic options reduce disease progression and improve quality of life in patients with cardiac amyloidosis?
Emerging therapies for cardiac amyloidosis, including TTR stabilizers and RNA interference, offer significant benefits in slowing disease progression and improving quality of life when initiated early.
Supports early use of these therapies in cardiac amyloidosis; confirms prognostic benefits in Level 1 evidence synthesis.
OBJECTIVE: The aim of this study was to identify emerging therapeutic options and the most effective treatments for patients with cardiac amyloidosis, assessing their clinical characteristics and discussing the impact of these interventions on reducing disease progression and improving quality of life.METHODS: A literature review was carried out using the Scielo and PubMed databases.A total of 297 articles were found, from which 18 studies that met the inclusion criteria were selected.RESULTS: Treatment of senile cardiac amyloidosis mainly involves measures to prevent and stop amyloid deposition, taking into account the patient's comorbidities.The importance of early diagnosis and administration of therapy before the condition evolves to significant cardiac dysfunction and other systemic manifestations is highlighted, since treatment is more effective in the early stages of the disease.Treatment is modulated according to risk stratification, aiming to offer greater comfort and survival to the patient, and requires the involvement of a multidisciplinary and competent team.CONCLUSION: The diagnosis of senile cardiac amyloidosis is challenging due to its nonspecific clinical manifestations, which often results in delayed treatment.The main therapeutic approaches have been chemotherapy with melphalan and prednisone, autologous stem cell transplantation (ASCT) and anti-plasma cell therapy in more advanced stages of the disease.With the advancement of therapies, a good prognosis and clinical improvement of patients has been observed.
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Almeida et al. (2023) conducted a review in Cardiac amyloidosis. Chemotherapy (melphalan and prednisone), autologous stem cell transplantation, and anti-plasma cell therapy was evaluated. Therapeutic approaches including melphalan, prednisone, autologous stem cell transplantation, and anti-plasma cell therapy improve clinical prognosis in patients with cardiac amyloidosis.
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