TY - JOUR
T1 - Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy
T2 - a longitudinal multicenter study in a non-endemic area
AU - Cortese, Andrea
AU - Vita, G.
AU - Luigetti, Marco
AU - Russo, M.
AU - Bisogni, Giulia
AU - Sabatelli, M.
AU - Manganelli, Fiore
AU - Santoro, L.
AU - Cavallaro, Tiziana
AU - Fabrizi, G. M.
AU - Schenone, Angelo
AU - Grandis, M.
AU - Gemelli, Chiara
AU - Mauro, Alessandro
AU - Pradotto, Luca
AU - Gentile, Luca
AU - Stancanelli, Claudia
AU - Lozza, Alessandro
AU - Perlini, Stefano
AU - Piscosquito, Giuseppe
AU - Calabrese, Daniela
AU - Mazzeo, A.
AU - Obici, Laura Piera
AU - Pareyson, Davide
PY - 2016/3/16
Y1 - 2016/3/16
N2 - Tafamidis is a transthyretin (TTR) stabilizer able to prevent TTR tetramer dissociation. There have been a few encouraging studies on Tafamidis efficacy in early-onset inherited transthyretin amyloidosis (ATTR) due to Val30Met mutation. However, less is known about its efficacy in later disease stages and in non-Val30Met mutations. We performed a multi-center observational study on symptomatic ATTR patients prescribed to receive Tafamidis. We followed up patients according to a standardized protocol including general medical, cardiological and neurological assessments at baseline and every 6 months up to 3 years. Sixty-one (42 males) patients were recruited. Only 28 % of enrolled subjects had the common Val30Met mutation, mean age of onset was remarkably late (59 years) and 18 % was in advanced disease stage at study entry. Tafamidis proved safe and well-tolerated. One-third of patients did not show significant progression along 36 months, independently from mutation type and disease stage. Neurological function worsened particularly in the first 6 months but progression slowed significantly thereafter. Autonomic function remained stable in 33 %, worsened in 56 % and improved in 10 %. Fifteen percent of patients showed cardiac disease progression and 30 % new onset of cardiomyopathy. Overall, Tafamidis was not able to prevent functional progression of the disease in 23 (43 %) subjects, including 16 patients who worsened in their walking ability and 12 patients who reached a higher NYHA score during the follow-up period. A higher mBMI at baseline was associated with better preservation of neurological function. In conclusion, neuropathy and cardiomyopathy progressed in a significant proportion of patients despite treatment. However, worsening of neurological function slowed after the first 6 months and also subjects with more advanced neuropathy, as well as patients with non-Val30Met mutation, benefited from treatment. Body weight preservation is an important favorable prognostic factor.
AB - Tafamidis is a transthyretin (TTR) stabilizer able to prevent TTR tetramer dissociation. There have been a few encouraging studies on Tafamidis efficacy in early-onset inherited transthyretin amyloidosis (ATTR) due to Val30Met mutation. However, less is known about its efficacy in later disease stages and in non-Val30Met mutations. We performed a multi-center observational study on symptomatic ATTR patients prescribed to receive Tafamidis. We followed up patients according to a standardized protocol including general medical, cardiological and neurological assessments at baseline and every 6 months up to 3 years. Sixty-one (42 males) patients were recruited. Only 28 % of enrolled subjects had the common Val30Met mutation, mean age of onset was remarkably late (59 years) and 18 % was in advanced disease stage at study entry. Tafamidis proved safe and well-tolerated. One-third of patients did not show significant progression along 36 months, independently from mutation type and disease stage. Neurological function worsened particularly in the first 6 months but progression slowed significantly thereafter. Autonomic function remained stable in 33 %, worsened in 56 % and improved in 10 %. Fifteen percent of patients showed cardiac disease progression and 30 % new onset of cardiomyopathy. Overall, Tafamidis was not able to prevent functional progression of the disease in 23 (43 %) subjects, including 16 patients who worsened in their walking ability and 12 patients who reached a higher NYHA score during the follow-up period. A higher mBMI at baseline was associated with better preservation of neurological function. In conclusion, neuropathy and cardiomyopathy progressed in a significant proportion of patients despite treatment. However, worsening of neurological function slowed after the first 6 months and also subjects with more advanced neuropathy, as well as patients with non-Val30Met mutation, benefited from treatment. Body weight preservation is an important favorable prognostic factor.
KW - Amyloid polyneuropathy
KW - Tafamidis
KW - Transthyretin
UR - http://www.scopus.com/inward/record.url?scp=84961207014&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84961207014&partnerID=8YFLogxK
U2 - 10.1007/s00415-016-8064-9
DO - 10.1007/s00415-016-8064-9
M3 - Article
SN - 0340-5354
SP - 1
EP - 9
JO - Journal of Neurology
JF - Journal of Neurology
ER -