| Literature DB >> 24859879 |
Arnaud Jaccard1, Raymond L Comenzo2, Parameswaran Hari3, Philip N Hawkins4, Murielle Roussel5, Pierre Morel6, Margaret Macro7, Jean-Luc Pellegrin8, Estibaliz Lazaro8, Dania Mohty9, Patrick Mercie8, Olivier Decaux10, Julian Gillmore4, David Lavergne11, Frank Bridoux12, Ashutosh D Wechalekar4, Christopher P Venner13.
Abstract
Bortezomib is an active agent in AL amyloidosis and responses to this drug in combination with cyclophosphamide and dexamethasone are both rapid and deep. Here we present an international, multicenter series of 60 patients with Mayo Clinic stage III cardiac amyloidosis to assess the impact of this regimen in improving outcomes in this poor-risk group. The median follow-up for the entire cohort is 11.8 months. The overall response rate was 68%. In a landmark analysis, examining patients who survived more than 3 months, the overall response rate was 86%. A cardiac response was seen in 32% of patients. The estimated 1-year survival rate for the whole cohort was 57% and 24 patients (40%) died while on therapy. Although unable to save the poorest risk patients, the combination of bortezomib, cyclophosphamide and dexamethasone can achieve a high number of hematologic and cardiac responses, likely improving overall survival and justifying a prospective trial. Copyright© Ferrata Storti Foundation.Entities:
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Year: 2014 PMID: 24859879 PMCID: PMC4562537 DOI: 10.3324/haematol.2014.104109
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941