Massimo Poidomani
University of Catania
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Publication
Featured researches published by Massimo Poidomani.
Bone Marrow Transplantation | 2007
P. De Fabritiis; Alessandra Spagnoli; P. Di Bartolomeo; Anna Locasciulli; L Cudillo; Giuseppe Milone; Alessandro Busca; Alessandra Picardi; Rosanna Scimè; Alessandro Bonini; L. Cupelli; P Chiusolo; Attilio Olivieri; Stella Santarone; Massimo Poidomani; Stefania Fallani; Andrea Novelli; Ignazio Majolino
Transplanted patients with a history of invasive fungal infection (IFI) are at high risk of developing relapse and fatal complications. Eighteen patients affected by hematological malignancies and a previous IFI were submitted to allogeneic stem cell transplantation, using Caspofungin as a secondary prophylaxis. Patients had a probable or proven fungal infection and 16 had a pulmonary localization. No side effects were recorded during treatment with Caspofungin. Compared to pre-transplant evaluation, stability or improvement of the previous IFI was observed in 16 of the 18 patients at day 30, in 13 of the 15 evaluable patients at day 180 and in 11 of the 11 evaluable patients at day 360 post transplant. In particular, all the six patients with a proven fungal infection were alive, with a stable or improved IFI after 1 year from transplant. At a maximum follow-up of 31 months, eight patients died for disease progression or transplant-related complications, but only two had evidence of fungal progression. Secondary prophylaxis with Caspofungin may represent a suitable approach to limit IFI relapse or progression, allowing patients with hematological malignancies to adhere to the planned therapeutic program.
International Journal of Hematology | 2004
Ugo Consoli; Amalia Figuera; Giuseppe Milone; Carmela Rita Meli; Giulia Guido; Francesco Indelicato; Gaetano Moschetti; Salvatore Leotta; Antonella Tornello; Massimo Poidomani; Pamela Murgano; Valeria Pinto; Rosario Giustolisi
Acute promyelocytic leukemia (APL) is characterized by onset at a young age and a life-threatening hemorrhagic diathesis, which is attributed to a disseminated intravascular coagulation (DIC)-like coagulopathy. The discovery of all-trans-retinoic acid has changed the course of APL treatment by reducing the onset of DIC and inducing a complete and durable remission in more than 90% of patients. The occurrence of APL during pregnancy is not a frequent event, but the management of these patients raises many therapeutic and ethical dilemmas and requires a careful clinical case evaluation of fetal and maternal risk, coagulation status, the parents’ wishes, and therapeutic options. Here we describe 3 patients with APL diagnosed during pregnancy. Clinical data and the therapeutic approaches are presented. In the discussion, we analyze clinical decisions and therapeutic options and compare our cases with those found in the literature. Int J Hematol. 2004;79:31-36.
Bone Marrow Transplantation | 2012
Giuseppe Milone; Massimo Poidomani; Salvatore Leotta; Giuseppe Avola; Maria Grazia Camuglia; Antonella Privitera; Carla Consoli; Salvatore Mercurio; M A Romeo; A. Di Marco; S Di Mercurio; Andrea Spadaro; G A Palumbo; P Tedeschi
Ninety-six AML patients in 1st CR were evaluated for peak CD34+ cell levels in peripheral blood (PB) during PBSC mobilization and harvest. Distribution of CD34+ cell peaks was determined and cases were grouped on the basis of 50th and 75th percentile: group A, those having a CD34+ cell peak ⩽70 × 109/L (n=48); group B, those having a CD34+ cell peak between 70 and 183 × 109/L (n=24); group C, those having a CD34+ cell peak >183 × 109/L (n=24). Irrespective of post-remission treatment received, group A had a disease free survival (DFS) of 73%, group B a DFS of 51% and group C of 30% (P=0.0003). In intermediate cytogenetic risk patients, those treated by autologous transplantation had a DFS of 68, 33 and 14% in the groups A, B and C, respectively, (P=0.01) whereas after allogeneic transplantation DFS was 87% in group A+B vs 50% in group C (P=0.009). The peak of CD34+ cells in PB, was an independent predictor for DFS in multivariate analysis.
Bone Marrow Transplantation | 2011
Salvatore Leotta; Massimo Poidomani; E Mauro; A Spadaro; E Marturano; Giuseppe Milone
AMD3100 for urgent PBSC mobilization and allogeneic transplantation from a normal donor after failed marrow harvest
Bone Marrow Transplantation | 2011
Carla Consoli; Salvatore Leotta; L Tambè; A. Di Marco; Giuseppe Avola; Maria Grazia Camuglia; S Di Mercurio; Massimo Poidomani; Giuseppe Milone
Inadvertent transplantation of haematopoietic stem cells carrying constitutional Robertsonian translocation from an apparently normal donor to an AML patient: a case report
Leukemia & Lymphoma | 2007
Giuseppe Milone; Salvatore Leotta; Katia Battiato; Pamela Murgano; Salvatore Mercurio; Aurora Strano; Massimo Poidomani; Stefania Coppoletta; Elisa Mauro; Giuseppe Avola; Valeria Pinto; Maria Grazia Camuglia; Rosario Giustolisi
We designed intermediate dose etoposide + G-CSF 16 µg/kg as a Peripheral Blood Stem Cell (PBSC) mobilization schedule suitable for outpatient administration. Forty-one Lymphoma patients received intermediate dose etoposide (200 mg/m2 i.v. day +1, +2, +3) +G-CSF 16 µg/kg/day. Results of PBSC mobilization in these patients were compared with those of a group of 37 lymphoma patients mobilized using cyclophosphamide (CTX) at dosage of 4 g/m2 + G-CSF 10 µg/kg/die. Mean peak of CD34+ cells achieved in P.B. and total CD34+ cells harvested were higher in patients mobilized with intermediate dose etoposide (p = 0.003 and p = 0.004, respectively). After transplantation recovery of polymorphonucleate neutrophils (PMN) > 0.5 × 109/L did not differ significantly between groups: 11.7 days in intermediate dose etoposide group and 11.5 days in CTX group (p = 0.7). Intermediate dose etoposide + G-CSF 16 µg/kg resulted in a maximum length of neutropenia (PMN < 0.5 × 109/L) of 2 days and neutropenic fever was registered during only 3/41 courses (7.3%). Intermediate dose etoposide + G-CSF 16 µg/kg is a highly effective mobilizing therapy, further, it has the advantage of low hematologic toxicity and can be easily administered as outpatient treatment.
Experimental Hematology | 2012
Giuseppe Milone; Giuseppe Avola; Salvatore Leotta; Aurora Strano; Maria Grazia Camuglia; Valeria Pinto; Salvatore Mercurio; Massimo Poidomani; Stefania Coppoletta; Anna Lia Di Marco; Carla Consoli; Anna Triolo; Andrea Spadaro; Antonella Privitera; Angela Ragusa; Daniele Tibullo; Sandra Di Mercurio
Blood | 2008
Giuseppe Milone; Massimo Poidomani; Stefania Coppoletta; E. Mauro; E. Marturano; F. Crispi; Andrea Spadaro; A. Di Marco; Salvatore Leotta
Blood | 2011
Giuseppe Milone; Massimo Poidomani; Salvatore Leotta; Valeria Pinto; Andrea Spadaro; Rita Lombardo
Blood | 2010
Giuseppe Milone; Salvatore Leotta; Giuseppe Avola; Massimo Poidomani; Maria Grazia Camuglia; Andrea Spadaro