Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy.
Rossella PariniPaola De LorenzoAndrea DardisAlberto BurlinaAlessandra CassioPaolo CavarzereDaniela ConcolinoRoberto Della CasaFederica DeodatoMaria Alice DonatiAgata FiumaraSerena GasperiniFrancesca MenniVeronica PagliardiniMichele SacchiniMarco SpadaRoberta TaurisanoMaria Grazia ValsecchiMaja Di RoccoBruno BembiPublished in: Orphanet journal of rare diseases (2018)
These data are the result of the longest independent retrospective study on ERT in IOPD reported so far outside clinical trials. The data obtained confirmed the better outcome of the CRIM-positive patients but at the same time, showed the inability of the current therapeutic approach to reverse or stabilize the disease progression. The results also evidenced the involvement of central nervous system in Pompe disease. To better understand the disease clinical history and to improve treatment efficacy larger multicentre studies are needed as well as the development of new therapeutic approaches.