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Maffioli, Margherita

https://orcid.org/0000-0002-2268-391X

Mayo Clinic

Ospedale di Circolo e Fondazione Macchi

Citations 12

A prognostic model to predict survival in 867 World Health Organization–defined essential thrombocythemia at diagnosis: a study by the International Working Group on Myelofibrosis Research and Treatment
Passamonti, Francesco , Thiele, Jürgen, Girodon, François , Rumi, Elisa , Carobbio, Alessandra , Gisslinger, Heinz , Kvasnicka, Hans Michael , Ruggeri, Marco , Randi, Maria Luigia , Gangat, Naseema , Gianatti, Andrea , Gisslinger, Bettina, Müllauer, Leonhard , Rodeghiero, Francesco, d'Amore, Emanuele S. G. , Bertozzi, Irene , Hanson, Curtis A. , Boveri, Emanuela , Marino, Filippo, Maffioli, Margherita , Antonioli, Elisabetta , Carrai, Valentina , Buxhofer‐Ausch, Veronika , Pascutto, Cristiana, Cazzola, Mario , Barbui, Tiziano , Tefferi, Ayalew , Vannucchi, Alessandro M. , dʼAmore, Emanuele S.G. , Caramazza, Domenica , Passamonti, Francesco , Cazzola, Mario

Blood | June 27, 2012 | Volume: 120 | Issue: 6 | Pages: 1197-1201

10.1182/blood-2012-01-403279 Get It

Abstract Diagnosis of essential thrombocythemia (ET) has been updated in the last World Health Organization (WHO) classification. We developed a prognostic model to predict survival at diagnosis, named IPSET (International Prognostic Score for ET), studying patients with WHO-defined ET. Age 60 years or older, leukocyte count ≥ 11 × 109/L, and prior thrombosis significantly affected survival, by multivariable Cox regression. On the basis of the hazard ratio, we assigned 2 points to age and 1 each to leukocyte count and thrombosis. So, the IPSET model allocated 867 patients into 3 risk categories with significantly different survival: low (sum of points = 0; median survival not reached), intermediate (sum = 1-2; median survival 24.5 years), and high (sum = 3-4, median survival 13.8 years). The IPSET model was further validated in 2 independent cohorts including 132 WHO-defined ET and 234 Polycythemia Vera Study Group–defined ET patients. The IPSET model was able to predict the occurrence of thrombosis, and not to predict post-ET myelofibrosis. In conclusion, IPSET, based on age ≥ 60 years, leukocyte count ≥ 11 × 109/L, and history of thrombosis allows prognostic assessment of WHO-defined ET and the validation process makes IPSET applicable in all patients phenotypically appearing as ET.
A dynamic prognostic model to predict survival in primary myelofibrosis: a study by the IWG-MRT (International Working Group for Myeloproliferative Neoplasms Research and Treatment)
Passamonti, Francesco , Cervantes, Francisco , Morra, Enrica, Rumi, Elisa , Pereira, Arturo , Guglielmelli, Paola , Pungolino, Ester , Caramella, Marianna, Maffioli, Margherita , Pascutto, Cristiana, Lazzarino, Mario, Cazzola, Mario , Tefferi, Ayalew , Vannucchi, Alessandro M. , Passamonti, Francesco , Cazzola, Mario , Guglielmelli, Paola

Blood | December 14, 2009 | Volume: 115 | Issue: 9 | Pages: 1703-1708

10.1182/blood-2009-09-245837 Get It

Abstract Age older than 65 years, hemoglobin level lower than 100 g/L (10 g/dL), white blood cell count greater than 25 × 109/L, peripheral blood blasts 1% or higher, and constitutional symptoms have been shown to predict poor survival in primary myelofibrosis (PMF) at diagnosis. To investigate whether the acquisition of these factors during follow-up predicts survival, we studied 525 PMF patients regularly followed. All 5 variables had a significant impact on survival when analyzed as time-dependent covariates in a multivariate Cox proportional hazard model and were included in 2 separate models, 1 for all patients (Dynamic International Prognostic Scoring System [DIPSS]) and 1 for patients younger than 65 years (age-adjusted DIPSS). Risk factors were assigned score values based on hazard ratios (HRs). Risk categories were low, intermediate-1, intermediate-2, and high in both models. Survival was estimated by the HR. When shifting to the next risk category, the HR was 4.13 for low risk, 4.61 for intermediate-1, and 2.54 for intermediate-2 according to DIPSS; 3.97 for low risk, 2.84 for intermediate-1, and 1.81 for intermediate-2 according to the age-adjusted DIPSS. The novelty of these models is the prognostic assessment of patients with PMF anytime during their clinical course, which may be useful for treatment decision-making.