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Risk factors for endocrine complications in transfusion-dependent thalassemia patients on chelation therapy with deferasirox: a risk assessment study from a multi-center nation-wide cohort.
Casale, Maddalena; Forni, Gian Luca; Cassinerio, Elena; Pasquali, Daniela; Origa, Raffaella; Serra, Marilena; Campisi, Saveria; Peluso, Angelo; Renni, Roberta; Cattoni, Alessandro; De Michele, Elisa; Allò, Massimo; Poggi, Maurizio; Ferrara, Francesca; Di Concilio, Rosanna; Sportelli, Filomena; Quarta, Antonella; Putti, Maria Caterina; Notarangelo, Lucia Dora; Sau, Antonella; Ladogana, Saverio; Tartaglione, Immacolata; Picariello, Stefania; Marcon, Alessia; Sturiale, Patrizia; Roberti, Domenico; Lazzarino, Antonio Ivan; Perrotta, Silverio.
Afiliação
  • Casale M; Department of Women, Child and General and Specialized Surgery, University " Luigi Vanvitelli", via Luigi De Crecchio n. 4, 80138, Naples. maddalena.casale@unicampania.it.
  • Forni GL; Center of Microcitemia and Congenital Anemias, Galliera Hospital, Mura delle Cappuccine 14 16128, Genoa.
  • Cassinerio E; Rare Diseases Center, General Medicine Unit, IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan.
  • Pasquali D; Endocrinology, Department of Advanced Medical and Surgical Sciences, University " Luigi Vanvitelli", Naples.
  • Origa R; Thalassemia Centre, Pediatric Hospital A CAO, AOG Brotzu, Cagliari.
  • Serra M; Thalassemia Centre, Department of Internal Medicine, Hospital "V. Fazzi", Lecce.
  • Campisi S; Thalassemia Centre, Hospital Umberto I, Siracusa.
  • Peluso A; Centre of Microcitemia, POC SS.Annunziata - ASL TA, Taranto.
  • Renni R; Thalassemia Centre, Department of Internal Medicine, Hospital F.Ferrari, Casarano.
  • Cattoni A; Department of Pediatrics, Università degli Studi di Milano Bicocca, Fondazione Monza e Brianza per il Bambino e la sua Mamma, Azienda Ospedaliera San Gerardo, Monza.
  • De Michele E; Immunotransfusion Medicine Unit, AOU OO.RR. S. Giovanni di Dio e Ruggi d'Aragona, Salerno.
  • Allò M; Centre of Microcitemia, Hospital ASL 5, Crotone.
  • Poggi M; Department of Endocrinology, Sant'Andrea Hospital, Rome.
  • Ferrara F; Department of Internal Medicine, Policlinico Hospital of Modena.
  • Di Concilio R; Department of Pediatrics, Hospital Umberto I, Nocera.
  • Sportelli F; Immunotransfusion Unit, Hospital Riuniti, Foggia.
  • Quarta A; Center for Microcythemia, Iron Metabolism disorders, Gaucher disease-Hematology and Transplantation Unit, "A. Perrino" Hospital, Brindisi.
  • Putti MC; Department of Women's and Child's Health (DSDB), University Hospital, Padova.
  • Notarangelo LD; Hematology Oncology Unit, Children's Hospital, ASST Spedali Civili, Brescia.
  • Sau A; Department of Pediatric Hematology and Oncology, Hospital "Spirito Santo", Pescara.
  • Ladogana S; Pediatric Oncohematology Unit, "Casa Sollievo della Sofferenza" Hospital, IRCCS, San Giovanni Rotondo.
  • Tartaglione I; Department of Women, Child and General and Specialized Surgery, University " Luigi Vanvitelli", via Luigi De Crecchio n. 4, 80138, Naples.
  • Picariello S; Department of Women, Child and General and Specialized Surgery, University " Luigi Vanvitelli", via Luigi De Crecchio n. 4, 80138, Naples.
  • Marcon A; Rare Diseases Center, General Medicine Unit, IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan.
  • Sturiale P; SSD Centre Of Microcitemia, G.O.M Reggio Calabria, Reggio Calabria.
  • Roberti D; Department of Women, Child and General and Specialized Surgery, University " Luigi Vanvitelli", via Luigi De Crecchio n. 4, 80138, Naples.
  • Lazzarino AI; EPISTATA - Agency for Clinical Research and Medical Statistics, London E8 3SY, United Kingdom.
  • Perrotta S; Department of Women, Child and General and Specialized Surgery, University " Luigi Vanvitelli", via Luigi De Crecchio n. 4, 80138, Naples.
Haematologica ; 107(2): 467-477, 2022 02 01.
Article em En | MEDLINE | ID: mdl-33406815
Transfusion-dependent patients typically develop iron-induced cardiomyopathy, liver disease, and endocrine complications. We aimed to estimate the incidence of endocrine disorders in transfusiondependent thalassemia (TDT) patients during long-term iron-chelation therapy with deferasirox (DFX). We developed a multi-center follow-up study of 426 TDT patients treated with once-daily DFX for a median duration of 8 years, up to 18.5 years. At baseline, 118, 121, and 187 patients had 0, 1, or ≥2 endocrine diseases respectively. 104 additional endocrine diseases were developed during the follow-up. The overall risk of developing a new endocrine complication within 5 years was 9.7% (95% Confidence Interval [CI]: 6.3-13.1). Multiple Cox regression analysis identified three key predictors: age showed a positive log-linear effect (adjusted hazard ratio [HR] for 50% increase 1.2, 95% CI: 1.1-1.3, P=0.005), the serum concentration of thyrotropin showed a positive linear effect (adjusted HR for 1 mIU/L increase 1.3, 95% CI: 1.1-1.4, P<0.001) regardless the kind of disease incident, while the number of previous endocrine diseases showed a negative linear effect: the higher the number of diseases at baseline the lower the chance of developing further diseasess (adjusted HR for unit increase 0.5, 95% CI: 0.4-0.7, P<0.001). Age and thyrotropin had similar effect sizes across the categories of baseline diseases. The administration of levothyroxine as a covariate did not change the estimates. Although in DFX-treated TDT patients the risk of developing an endocrine complication is generally lower than the previously reported risk, there is considerable risk variation and the burden of these complications remains high. We developed a simple risk score chart enabling clinicians to estimate their patients' risk. Future research will look at increasing the amount of variation explained from our model and testing further clinical and laboratory predictors, including the assessment of direct endocrine magnetic resonance imaging.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Talassemia / Talassemia beta / Sobrecarga de Ferro Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Talassemia / Talassemia beta / Sobrecarga de Ferro Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article