Dr. Antonio Spadano
EMATOLOGO

Su di me
Specialista in Ematologia clinica e di laboratorio, Oncologia medica e Medicina dello sport, direttore della struttura semplice di Chemioterapia ad alte dosi dal 2000 e Primario dell’ematologia clinica dal 2018 al 2020.
Negli anni della sua attività clinica presso l’Ospedale Spirito Santo di Pescara ha svolto anche attività di didattica ed è autore di numerose pubblicazioni scientifiche su riviste nazionali ed internazionali.
In collaborazione con Gruppi di studio Nazionali ed Internazionali, ha svolto ricerca in ambito ematologico presso il reparto di Ematologia di Pescara.
Campi d’interesse medico e scientifico:
Gammopatie monoclonali e discrasie plasmacellulari: MGUS, Mieloma Multiplo, Amiloidosi
Leucemie mieloidi e linfoidi acute e croniche
Linfoadenomegalie e Disordini linfoproliferativi
Anemie congenite e acquisite
Citopenie: piastrinopenie, neutropenie, linfocitopenie
Sindromi mieloproliferative croniche: Policitemia vera, Trombocitemia essenziale, Mielofibrosi
Sindromi Mielodisplastiche
Malattie emorragiche e trombotiche congenite e acquisite
Disordini del bilancio ferro
Genetica delle malattie ematologiche
Splenomegalie
Patologie Trattate
Anemia
Piastrinopenia
Linfoma
Leucemia
Gammapatie monoclonali
Leucemie croniche
Immunodeficienza
Leucemia Mieloide Cronica
Emocromatosi
Patologie genetiche
Specializzazioni
- Ematologia
Formazione
- 29/12/1978 – MEDICINA E CHIRURGIA (PAVIA)
- 30/12/1982 – EMATOLOGIA GENERALE (CHIETI GABRIELE D’ANNUNZIO) – Specializzazione
Pubblicazioni
- Remission-induction, consolidation and maintenance therapy by AVA protocol in acute non lymphoblastic leukemia. Hematologica. 67, 230, 1982.
- Il nucleoside 9-(1,3 dihydroxy-2-proproxymetil) guanina nella terapia della corioretinite da CMV in un paziente con AIDS. AIDS e Sindromi correlate a cura di F. Aiuti, M. Moroni e F. Pocchiari. Monduzzi Editore pag. 375, Roma, maggio 1987
- Trattamento dell’Emofilia A e sindromi correlate con crioprecipitati di FVIII “virus inattivati” Panta Rei Volume VI, Fascicolo 3-4, 1987
- Cytogenetics and acute non lymphocytic leukemia. Ann Genet. 1987;30(1):39-46.PMID: 3498428
- Meaning of chromosome 6 aberrations in Ph’-positive chronic granulocytic leukemia. Haematologica. 1984 Nov-Dec;69(6):661-70.
- Rieve AK Chronic granulocytic leukemia with loss of Philadelphia chromosome and development of a Philadelphia negative diploid clone. Haematologica. 1984 May-Jun;69(3):321-9.
- Chromosome anomalies and Waldenström’s macroglobulinemia Pathologica. 1983 Nov-Dec;75(1040):861-6.
- Alpha heavy chain disease: report of two cases. Haematologica. 1985 Sep-Oct;70(5):431-6.
- Plasma exchange as intensive therapy in thrombotic thrombocytopenic purpura. Haematologica. 1985 May-Jun;70(3):225-31.
- Chromosome changes in 19 patients with Waldenström’s macroglobulinemia. Cancer Genet Cytogenet. 1987 Dec;29(2):261-9.
- Autologous blood stem cell transplantation as intensive consolidation therapy in hematological malignancies. Haematologica. 1990 Jan-Feb;75 Suppl 1:60-4.
- Cytogenetic survey of sixty-one patients with preleukemic syndrome including myeloproliferative and myelodysplastic diseases. Ann Genet. 1990;33(4):214-8.
- Randomized comparison of Ceftriaxone versus Ceftriaxone plus Amikacin for the empirical treatment of infections in patiens with altered host defense: microbiological and clinical evaluation. Experimental Chemioterapy 38: 420-427,1992.
- Randomized comparison of ceftriaxone vs ceftriaxone plus amikacin for the empirical treatment of infections in patients with altered host defense. Microbiological and clinical evaluation. Chemotherapy 1992;38:420-7.
- Autologous blood stem cell transplantation in malignant lymphoma: an Italian Cooperative Study. Leukemia and Lymphoma 1992;7(1):11-16.
- The result of various tratment in TTP; a report of 18 Episodes in 12 patients Transfus Sci 13: 91-971992
- Complex translocations of the Ph chromosome and Ph negative CML arise from similar mechanisms, as evidenced by FISH analysis. Cancer Genet Cytogenet. 1994 Dec;78(2):153-9.
- Leukemic evolution in three patients with myelodysplastic syndrome and unusual chromosome changes. Cancer Genet Cytogenet. 1992 Jul 15;61(2):162-4.
- Cytogenetic survey on 80 patients with acute non-lymphocytic leukemia”. Cancer Genet Cytogenet, 59: 45-50, 1992.
- Leukemic evolution in three patients with myelodisplastic syndrome and unusual chromosome changes”. Cancer Genet Cytogenet, 61:162-164, 1992.
- Complex translocation of the Ph chromosome and Ph negative CML arise from similar mechanisms as evidenced by FISH analysis. Cancer Genet Cytogenet, 78:153-159, 1994.
- p53 loss and point mutations are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis. Cancer Genet Cytogenet, 1997 Oct 1;98(1):28-35
- Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping. Haematologica. 2000 Nov;85(11):1219-21.
- Spectral karyotyping (SKY) refinement of a complex karyotype with t(20; 21) in a Ph-positive CML patient submitted to peripheral blood stem cell transplantation. Bone Marrow Transplant 2000, Vol 26, 1125-27.
- Preliminary Data of Phase I Clinical Trial with Autologous Cytokine Induced Killer cells in Patients with Advanced Malignancies. Blood 2003, 102, 11: p57b, 3933.
- Large volume leukapheresis with AMICUS cell separator in peripheral blood stem cell autologous transplant. Transfus Apher Sci. 2001 Feb;24(1):79-83.
- Karyotype refinement by multicolor fluorescence in situ hybridization analysis in 18 patients with acute lymphoblastic leukemia. Haematologica. 2002 Aug;87(8):888-9.
- Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts (RAEB). Br J Haematol. 2003 Sep;122(5):760-3.
- Survival of elderly patients with acute myeloid leukemia. Haematologica. 2004 Mar;89(3):296-302.
- Inositide-specific phospholipase c beta1 gene deletion in the progression of myelodysplastic syndrome to acute myeloid leukemia. Leukemia.2004 Jun;18(6):1122-6.
- Acquired haemophilia masked by heparin therapy. Int J Immunopathol Pharmacol. 2004 May-Aug;17(2):227-8.
- Impact of a new dosing regimen of epoetin alfa on quality of life and anemia in patients with low-risk myelodysplastic syndrome. Ann Hematol. 2005 Mar;84(3):167-76. Epub 2004 Nov 30.
- Long term remission in BCR/ABL positive AML-M6 patient treated with Imatinib Mesylate.. Leukemia Research, April 2007, 31(4):563-567 (pubblicato online il 14 agosto 2006).
- Leukemia. 2007 Nov;21(11):2373-5. Epub 2007 Jun 21.
- Portal venous thrombosis in a young patient with idiopathic myelofibrosis and intrahepatic extramedullary hematopoiesis: a difficult diagnosis, prognosis and management.
- Is JAK2V617F mutation absence a risk factor for bleeding in Essential Thrombocythemia? An analysis on 106 patients. Blood Transfusion. 2010 Jan;8(1):21-7
- GIMEMA Italian Myeloma Network Bortezomib with thalidomide plus dexamethasone compared with thalidomide plus dexamethasone as induction therapy before, and consolidation therapy after, double autologous stem-cell transplantation in newly diagnosed multiple myeloma: a randomised phase 3 study. Lancet. 2010 Dec 18;376(9758):2075-85
- Tale of a Bacteraemia by Rhodococcus equi, With Concomitant Lung Mass: What Came First, the Chicken or The Egg? Mediterr J Hematol Infect Dis. 2011
- Bortezomib-thalidomide-dexamethasone is superior to thalidomide-dexamethasone as consolidation therapy after autologous hematopoietic stem cell transplantation in patients with newly diagnosed multiple myeloma. Blood. 2012 Jul 5;120(1):9-19
- TET2 mutations in Ph-negative myeloproliferative neoplasms: identification of three novel mutations and relationship with clinical and laboratory findings. Biomed Res Int. 2013;2013:929840
Competenze Linguistiche
- Italiano