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Featured researches published by Annamaria Nosari.


Haematologica | 2010

Invasive aspergillosis in patients with acute myeloid leukemia: a SEIFEM-2008 registry study.

Livio Pagano; Morena Caira; Anna Candoni; Massimo Offidani; Bruno Martino; Giorgina Specchia; Domenico Pastore; Marta Stanzani; Chiara Cattaneo; Rosa Fanci; Cecilia Caramatti; Fausto Rossini; Mario Luppi; Leonardo Potenza; Felicetto Ferrara; Maria Enza Mitra; Rafaela Maria Fadda; Rosangela Invernizzi; Teresa Aloisi; Marco Picardi; Alessandro Bonini; Adriana Vacca; Anna Chierichini; Lorella Melillo; Chiara De Waure; Luana Fianchi; Marta Riva; Giuseppe Leone; Franco Aversa; Annamaria Nosari

Background The aim of this study was to evaluate prognostic factors, treatments and outcome of invasive aspergillosis in patients with acute myeloid leukemia based on data collected in a registry. Design and Methods The registry, which was activated in 2004 and closed in 2007, collected data on patients with acute myeloid leukemia, admitted to 21 hematologic divisions in tertiary care centers or university hospitals in Italy, who developed proven or probable invasive aspergillosis. Results One hundred and forty cases of invasive aspergillosis were collected, with most cases occurring during the period of post-induction aplasia, the highest risk phase in acute myeloid leukemia. The mortality rate attributable to invasive aspergillosis was 27%, confirming previous reports of a downward trend in this rate. Univariate and multivariate analyses revealed that the stage of acute myeloid leukemia and the duration of, and recovery from, neutropenia were independent prognostic factors. We analyzed outcomes after treatment with the three most frequently used drugs (liposomal amphotericin B, caspofungin, voriconazole). No differences emerged in survival at day 120 or in the overall response rate which was 71%, ranging from 61% with caspofungin to 84% with voriconazole. Conclusions Our series confirms the downward trend in mortality rates reported in previous series, with all new drugs providing similar survival and response rates. Recovery from neutropenia and disease stage are crucial prognostic factors. Efficacious antifungal drugs bridge the period of maximum risk due to poor hematologic and immunological reconstitution.


British Journal of Haematology | 1997

Mucormycosis in patients with haematological malignancies: a retrospective clinical study of 37 cases

Livio Pagano; Paolo Ricci; Anna Tonso; Annamaria Nosari; Laura Cudillo; Marco Montillo; Annarita Cenacchi; Leonardo Pacilli; Francesco Fabbiano; Albano Del Favero

A retrospective study of 37 patients with haematological malignancy (21 acute myeloid leukaemia, 11 acute lymphoid leukaemia, two lymphoma, two hairy cell leukaemia, one Hodgkins disease) and histologically documented mucormycosis was conducted to evaluate the clinical characteristics and ascertain the factors which influenced the outcome from mycotic infection. Patients were admitted to 18 haematology divisions in tertiary care or university hospitals in Italy between 1987 and 1995.


Journal of Clinical Oncology | 2003

High-dose therapy and autologous peripheral-blood stem-cell transplantation as salvage treatment for HIV-associated lymphoma in patients receiving highly active antiretroviral therapy.

Alessandro Re; Chiara Cattaneo; Mariagrazia Michieli; Salvatore Casari; Michele Spina; Maurizio Rupolo; Bernardino Allione; Annamaria Nosari; Clara Schiantarelli; Mariagrazia Viganò; Immacolata Izzi; Piero Ferremi; Arnalda Lanfranchi; Maurizio Mazzuccato; Gianpiero Carosi; Umberto Tirelli; Giuseppe Rossi

PURPOSE High-dose therapy (HDT) and peripheral-blood stem-cell transplantation (PBSCT) in HIV-associated lymphoma (HIV-Ly) has been recently reported in selected patients. We describe the results of a multi-institutional program of HDT and PBSCT as salvage therapy in HIV-Ly responsive to highly active antiretroviral therapy (HAART) in unselected patients. PATIENTS AND METHODS Patients with resistant or relapsed HIV-Ly after first-line chemotherapy (CT) underwent PBSC collection after a course of second-line CT or cyclophosphamide and granulocyte colony-stimulating factor. Patients with chemotherapy-sensitive disease received carmustine, etoposide, cytarabine, and melphalan (BEAM regimen) and PBSC reinfusion. Effective HAART was maintained during the entire program. RESULTS Sixteen consecutive patients entered the program. Adequate collection of PBSC was obtained in 80% of patients (median CD34+ cells 6.8 x 106/kg). Three patients had early progression. Ten patients (62%) received PBSCT with prompt engraftment in all patients (neutrophils and platelet engraftment after a median of 10 days [range, 8 to 10 days] and 13 days [range, 8 to 18 days], respectively). No patients died as a result of opportunistic or other infections or treatment-related complications. Eight of nine assessable patients achieved complete remission (one patient after radiotherapy for residual disease) and one patient achieved partial remission. Two patients experienced relapse and died at +10 and +14 months. Six patients are alive and disease free at a median of 8 months after transplantation. CONCLUSION Our data confirm that HDT plus PBSCT is feasible and active as salvage therapy in HIV-Ly on a multi-institutional basis and in unselected HAART-responding patients. HIV infection should no longer preclude the opportunity of HDT in patients with lymphoma.


British Journal of Haematology | 2002

Pneumocystis carinii pneumonia in patients with malignant haematological diseases: 10 years' experience of infection in GIMEMA centres

Livio Pagano; Luana Fianchi; Luca Mele; Corrado Girmenia; Massimo Offidani; Paolo Ricci; Maria Enza Mitra; Marco Picardi; Cecilia Caramatti; Paolo Piccaluga; Annamaria Nosari; Massimo Buelli; Bernardino Allione; Agostino Cortelezzi; Francesco Fabbiano; Giuseppe Milone; Rosangela Invernizzi; Bruno Martino; Luciano Masini; Giuseppe Todeschini; Maria A. Cappucci; Domenico Russo; Laura Corvatta; Pietro Martino; Albano Del Favero

Summary. A retrospective survey was conducted over a 10‐year period (1990–99) among 52 haematology divisions in order to evaluate the clinical and laboratory characteristics and outcome of patients with proven Pneumocystis carinii pneumonia (PCP) complicating haematological diseases. The study included 55 patients (18 with non‐Hodgkins lymphoma, 10 with acute lymphoblastic leukaemia, eight with acute myeloid leukaemia, five with chronic myeloid leukaemia, four with chronic lymphocytic leukaemia, four with multiple myeloma, three with myelodysplastic syndrome, two with myelofibrosis and one with thalassemia) who developed PCP. Among these, 18 (33%) underwent stem cell transplantation; only two received an oral prophylaxis with trimethroprim/sulphamethoxazole. Twelve patients (22%) developed PCP despite protective isolation in a laminar airflow room. The most frequent symptoms were: fever (86%), dyspnoea (78%), non‐productive cough (71%), thoracic pain (14%) and chills (5%); a severe hypoxaemia was present in 39 patients (71%). Chest radiography or computerized tomography showed interstitial infiltrates in 34 patients (62%), alveolar infiltrates in 12 patients (22%), and alveolar–interstitial infiltrates in nine patients (16%). Bronchoalveolar lavage was diagnostic in 47/48 patients, induced sputum in 9/18 patients and lung biopsy in 3/8 patients. The diagnosis was made in two patients at autopsy. All patients except one started a specific treatment (52 patients trimethroprim/sulphamethoxazole, one pentamidine and one dapsone). Sixteen patients (29%) died of PCP within 30 d of diagnosis. Multivariate analysis showed that prolonged steroid treatment (P < 0·006) and a radiological picture of diffuse lung involvement (P < 0·003) were negative diagnostic factors.


European Journal of Haematology | 2009

Retrospective study of candidemia in patients with hematological malignancies. Clinical features, risk factors and outcome of 76 episodes

Livio Pagano; Andrea Antinori; Adriana Ammassari; Luca Mele; Annamaria Nosari; Lorella Melillo; Bruno Martino; Maurizio Sanguinetti; Francesco Equitani; Francesco Nobile; Mario Carotenuto; Enrica Morra; Giulia Morace; Giuseppe Leone

A retrospective study of 76 episodes of candidemia in 73 patients with underlying hematological malignancy, from 1988 until 1997, has been conducted to evaluate the clinical characteristics and to ascertain the variables related to the onset and the outcome of candidemia. The most frequent malignancy was acute myeloid leukemia (29 episodes). Candidemia developed mainly during aplasia in patients refractory to chemotherapy (42%). In 65 episodes (86%) the patients were neutropenic (ANC < 1×109/l) before the candidemia diagnosis for a median time of 13 d, and in 53 episodes (70%) at microbiological diagnosis of candidemia ANC was <1×109/l. Candida albicans was the most frequently isolated etiologic agent (31 episodes), but C. non‐albicans species sustained the majority of candidemia. Seventeen candidemias developed during azoles prophylaxis. One month after the diagnosis of candidemia, 26 patients died. In 19 cases, death was attributable to candidemia. The case‐control study demonstrated, at univariate analysis, that the colonization with Candida, spp. (p=0.004), antimycotic prophylaxis (p=0.01), presence of central venous catheter (p=0.01), neutropenia (p=0.002), and the use of glycopeptide (p=0.0001) increased the risk of candidemia. Using multivariate regression analysis only colonization with Candida spp. and the previous therapy with glycopeptide were associated with a significantly increased risk. Acute mortality, expressed by a cumulative probability of survival at 30 d from diagnosis of candidemia, was 0.67 (95% C.I. 0.55–0.77) and was significantly reduced in patients with neutrophils <1×109/l when compared to those with neutrophils > 1×109/l (p at Mantel‐Cox=0.029). Overall cumulative probability of survival at 1 yr was 0.38 (95% C.I. 0.27–0.49) and only the treatment with Amfotericin B significantly reduced the risk of death.


British Journal of Haematology | 1995

Fatal haemoptysis in pulmonary filamentous mycosis: An underevaluated cause of death in patients with acute leukaemia in haematological complete remission. A retrospective study and review of the literature

Livio Pagano; Paolo Ricci; Annamaria Nosari; Anna Tonso; Massimo Buelli; Marco Montillo; Laura Cudillo; Annarita Cenacchi; Chiara Savignana; Lorella Melillo; Anna Chierichini; Roberto Marra; Giampaolo Bucaneve; Giuseppe Leone; Albano Del Favero

A retrospective study on a consecutive series of 116 patients affected by acute leukaemia with documented pulmonary filamentous mycosis (FM) admitted between 1987 and 1992 to 14 tertiary‐care hospitals in Italy was made in order to evaluate the characteristics of those patients who developed fatal massive haemoptysis.


Clinical Infectious Diseases | 2012

Evaluation of the Practice of Antifungal Prophylaxis Use in Patients With Newly Diagnosed Acute Myeloid Leukemia: Results From the SEIFEM 2010-B Registry

Livio Pagano; Morena Caira; Anna Candoni; Franco Aversa; Carlo Castagnola; Cecilia Caramatti; Chiara Cattaneo; Mario Delia; Maria Rosaria De Paolis; Roberta Di Blasi; Luigi Di Caprio; Rosa Fanci; Mariagrazia Garzia; Bruno Martino; Lorella Melillo; Maria Enza Mitra; Gianpaolo Nadali; Annamaria Nosari; Marco Picardi; Leonardo Potenza; Prassede Salutari; Enrico Maria Trecarichi; Mario Tumbarello; Luisa Verga; Nicola Vianelli; Alessandro Busca

BACKGROUND To analyze the efficacy of antifungal prophylaxis (AFP) with posaconazole and itraconazole in a real-life setting of patients with acute myeloid leukemia (AML) during the first induction of remission. METHODS From January 2010 to June 2011, all patients with newly diagnosed AML were consecutively registered and prospectively monitored at 30 Italian hematological centers. Our analysis focused on adult patients who received intensive chemotherapy and a mold-active AFP for at least 5 days. To determine the efficacy of prophylaxis, invasive fungal disease (IFD) incidence, IFD-attributable mortality, and overall survival were evaluated. RESULTS In total, 515 patients were included in the present analysis. Posaconazole was the most frequently prescribed drug (260 patients [50%]) followed by fluconazole (148 [29%]) and itraconazole (93 [18%]). When comparing the groups taking posaconazole and itraconazole, there were no significant differences in the baseline clinical characteristics, whereas there were significant differences in the percentage of breakthrough IFDs (18.9% with posaconazole and 38.7% with itraconazole, P< .001). The same trend was observed when only proven/probable mold infections were considered (posaconazole, 2.7% vs itraconazole, 10.7%, P= .02). There were no significant differences in the IFD-associated mortality rate, while posaconazole prophylaxis had a significant impact on overall survival at day 90 (P= .002). CONCLUSIONS During the last years, the use of posaconazole prophylaxis in high-risk patients has significantly increased. Although our study was not randomized, it demonstrates in a real-life setting that posaconazole prophylaxis confers an advantage in terms of both breakthrough IFDs and overall survival compared to itraconazole prophylaxis. CLINICAL TRIALS REGISTRATION NCT01315925.


Haematologica | 2011

The use and efficacy of empirical versus pre-emptive therapy in the management of fungal infections: the HEMA e-Chart Project

Livio Pagano; Morena Caira; Annamaria Nosari; Chiara Cattaneo; Rosa Fanci; Alessandro Bonini; Nicola Vianelli; Maria Grazia Garzia; Mario Mancinelli; Maria Elena Tosti; Mario Tumbarello; Pierluigi Viale; Franco Aversa; Giuseppe Rossi

Background Neutropenic patients with persistent fever despite antibiotic therapy are managed with empirical or pre-emptive antifungal therapy. The aim of the present study was to evaluate the current clinical use and efficacy of these two approaches in patients with high risk hematologic conditions. Design and Methods An electronic medical record system, the “Hema e-Chart”, was designed and implemented to collect information prospectively on infectious complications, particularly on invasive fungal diseases, in patients with hematologic malignancies treated with chemotherapy and/or autologous or allogenic hemopoietic stem cell transplantation. The patients were enrolled from Hematology units distributed widely across Italy. Results Three hundred and ninety-seven adults with hematologic malignancies treated with chemotherapy with persistent fever and suspected invasive fungal disease were evaluable for the study (190 treated had been treated with empirical antifungal therapy and 207 with preemptive antifungal therapy). There was a significantly lower incidence of proven/probable invasive fungal diseases in patients treated with empirical antifungal therapy (n=14, 7.4%) than in patients treated with pre-emptive therapy (n=49, 23.7%) (P<0.001). The rate of deaths attributable to invasive fungal diseases was significantly lower in subjects treated with empirical antifungal therapy (1 case; 7.1%) than in subjects treated with pre-emptive therapy (11 cases; 22.5%) (P=0.002). Conclusions These data indicate that empirical antifungal treatment decreased the incidence of invasive fungal disease and of attributable mortality with respect to a pre-emptive antifungal approach in neutropenic febrile patients with hematologic malignancies. (ClinicalTrials.gov Identifier: NCT01069887)


Journal of Chemotherapy | 2009

Zygomycosis in Italy: a Survey of FIMUA-ECMM (Federazione Italiana di Micopatologia Umana ed Animale and European Confederation of Medical Mycology)

Livio Pagano; Caterina Giovanna Valentini; Brunella Posteraro; Corrado Girmenia; C. Ossi; A. Pan; Anna Candoni; Annamaria Nosari; Marta Riva; Chiara Cattaneo; Fausto Rossini; Luana Fianchi; Morena Caira; Maurizio Sanguinetti; Giovanni Gesu; Gianluigi Lombardi; Nicola Vianelli; Marta Stanzani; E. Mirone; G. Pinsi; Fabio Facchetti; N. Manca; L. Savi; M. Mettimano; V. Selva; I. Caserta; P. Scarpellini; Giulia Morace; A d'Arminio Monforte; Paolo Grossi

Abstract The aims of the study were to analyze the clinical and epidemiological characteristics and treatments for patients who developed zygomycosis enrolled in italy during the european Confederation of medical mycology survey. This prospective multicenter study was performed between 2004 and 2007 at 49 italian Departments. 60 cases of zygomycosis were enrolled: the median age was 59.5 years (range 1-87), with a prevalence of males (70%). The majority of cases were immunocompromised patients (42 cases, 70%), mainly hematological malignancies (37). Among non-immunocompromised (18 cases, 30%), the main category was represented by patients with penetrating trauma (7/18, 39%). The most common sites of infection were sinus (35%) with/without CNS involvement, lung alone (25%), skin (20%), but in 11 cases (18%) dissemination was observed. According to EORTC criteria, the diagnosis of zygomycosis was proven in 46 patients (77%) and in most of them it was made in vivo (40/46 patients, 87%); in the remaining 14 cases (23%) the diagnosis was probable. 51 patients received antifungal therapy and in 30 of them surgical debridement was also performed. The most commonly used antifungal drug was liposomal amphotericin b (L- AmB), administered in 44 patients: 36 of these patients (82%) responded to therapy. Altogether an attributable mortality rate of 32% (19/60) was registered, which was reduced to 18% in patients treated with L-AmB (8/44). Zygomycosis is a rare and aggressive filamentous fungal infection, still associated with a high mortality rate. This study indicates an inversion of this trend, with a better prognosis and significantly lower mortality than that reported in the literature. It is possible that new extensive, aggressive diagnostic and therapeutic procedures, such as the use of L-AmB and surgery, have improved the prognosis of these patients.


Haematologica | 2011

Multidrug resistant Pseudomonas aeruginosa bloodstream infection in adult patients with hematologic malignancies

Enrico Maria Trecarichi; Mario Tumbarello; Morena Caira; Anna Candoni; Chiara Cattaneo; Domenico Pastore; Rosa Fanci; Annamaria Nosari; Nicola Vianelli; Alessandro Busca; Antonio Spadea; Livio Pagano

We read with interest the article by Caselli et al. [1][1] who described a 9-year retrospective series of Pseudomonas aeruginosa (PA) bacteremia cases from 12 Italian pediatric hematology oncology centers and reported a total of 127 patients with Pseudomonas aeruginosa bloodstream infections (BSIs

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Livio Pagano

Catholic University of the Sacred Heart

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Morena Caira

Catholic University of the Sacred Heart

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Rosa Fanci

Catholic University of the Sacred Heart

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Marco Picardi

University of Naples Federico II

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Marco Montillo

Catholic University of the Sacred Heart

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