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Dive into the research topics where Aspasia Georgala is active.

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Featured researches published by Aspasia Georgala.


Journal of Clinical Oncology | 2006

Outpatient oral antibiotics for febrile neutropenic cancer patients using a score predictive for complications

Jean Klastersky; Marianne Paesmans; Aspasia Georgala; Frédérique Muanza; Barbara Plehiers; Laurent Dubreucq; Yassine Lalami; Michel Aoun; Martine Barette

PURPOSE Since febrile neutropenic patients were recognized to constitute a heterogeneous population, several models have been developed for predicting the risk of serious medical complications. The Multinational Association for Supportive Care in Cancer score and its derived clinical prediction rules have been validated, but thus far there were no data about its use for simplifying therapy in predicted low-risk patients. PATIENTS AND METHODS In a single institution, we followed all episodes of febrile neutropenia between January 1999 and November 2003. Those patients predicted at low risk for complications, who were not receiving antibacterials at fever onset and were eligible for treatment with oral antibiotics, were treated with ciprofloxacin and amoxicillin-clavulanate and were discharged if they were clinically stable or improving after an initial observation period. The primary end point of the study was the rate of resolution of the febrile neutropenic episode without complications, among these early discharged patients. RESULTS Of 383 first febrile neutropenic episodes predicted at low risk of complication, 178 patients (33 men and 145 women, mainly with solid tumors) were treated orally; they constituted the basis of our analysis. Seventy-nine patients (44%) were discharged early (with a median time to discharge of 26 hours); no complications occurred among them but three patients had to be readmitted, resulting in a success rate of 96% (95% CI, 92% to 100%). CONCLUSION Our study shows that oral therapy followed by early discharge was feasible in a small but significant proportion of patients selected by a strategy combining predicted low risk and medical and nonmedical criteria.


Clinical Infectious Diseases | 2005

Intravesical Instillation of Cidofovir in the Treatment of Hemorrhagic Cystitis Caused by Adenovirus Type 11 in a Bone Marrow Transplant Recipient

Panagiotis Fanourgiakis; Aspasia Georgala; Marc Vekemans; Agnès Triffet; Jean-Marc De Bruyn; Valérie Duchateau; Philippe Martiat; Erik De Clercq; Robert Snoeck; Elke Wollants; Annabel Rector; Marc Van Ranst; Michael F. Aoun

Hemorrhagic cystitis that occurs late after bone marrow transplantation (BMT) in BMT recipients is often associated with adenovirus or polyomavirus BK infections. Intravesical instillation of cidofovir in a BMT recipient with intractable hemorrhagic cystitis resulted in clinical improvement. Local cidofovir therapy for viral hemorrhagic cystitis could be an alternative to intravenous administration of cidofovir.


Clinical Infectious Diseases | 2007

Low Mannose-Binding Lectin Concentration Is Associated with Severe Infection in Patients with Hematological Cancer Who Are Undergoing Chemotherapy

Marcel Vekemans; James Owen Robinson; Aspasia Georgala; Corine Heymans; Frédérique Muanza; Marianne Paesmans; Jean Klastersky; Martine Barette; Nathalie Meuleman; Françoise Huet; Thierry Calandra; Sabrina Costantini; Alain Ferrant; F. Mathissen; M. Axelsen; Oscar Marchetti; Michel Aoun

BACKGROUND Mannose-binding lectin (MBL) is a serum lectin involved in innate immune response. Low serum MBL concentration may constitute a risk factor for infection in patients receiving myelosuppressive chemotherapy. METHODS We conducted a prospective, observational study that assessed MBL concentration as a risk factor for infection in patients with hematological malignancy who were hospitalized to undergo at least 1 chemotherapy cycle. MBL deficiency was defined using an algorithm that considered the serum MBL concentration and the MBL genotype. The primary end point was the ratio of duration of febrile neutropenia to the duration of neutropenia. Secondary end points included the incidence of severe infection (e.g., sepsis, pneumonia, bacteremia, and invasive fungal infection). Logistic regression analysis was conducted, and Fishers exact test was used to analyze binary outcomes, and Kaplan-Meier estimates and log rank tests were used for time-to-event variables. RESULTS We analyzed 255 patients who received 569 cycles of chemotherapy. The median duration of neutropenia per cycle was 7 days (interquartile range, 0-13 days). Sixty-two patients (24%) were found to have MBL deficiency. Febrile neutropenia occurred at least once in 200 patients. No difference in the primary outcome was seen. The incidence of severe infection was higher among MBL-deficient patients than among non-MBL-deficient patients (1.96 vs. 1.34 cases per 100 days for analysis of all patients [P=.008] and 1.85 vs. 0.94 cases per 100 days excluding patients with acute leukemia [P<.001]). CONCLUSIONS MBL deficiency does not predispose adults with hematological cancer to more-frequent or more-prolonged febrile episodes during myelosuppressive chemotherapy, but MBL-deficient patients have a greater number of severe infections and experience their first severe infection earlier, compared with nondeficient patients.


Annals of Oncology | 2008

A general chemotherapy myelotoxicity score to predict febrile neutropenia in hematological malignancies

Michel Moreau; Jean Klastersky; A Schwarzbold; Frédérique Muanza; Aspasia Georgala; Michel Aoun; Angela Loizidou; Martine Barette; Sabrina Costantini; Michel Delmelle; Laurent Dubreucq; Marc Vekemans; Augustin Ferrant; Dominique Bron; Marianne Paesmans

BACKGROUND Chemotherapy-induced neutropenia is the most common adverse effect of chemotherapy and is often complicated by febrile neutropenia (FN). The objective of this study is to validate a classification of aggressiveness of a chemotherapy regimen and to evaluate its usefulness in a risk prediction model of FN in patients with hematological cancer at the beginning of a chemotherapy cycle. PATIENTS AND METHODS Two hundred and sixty-six patients were prospectively enrolled and followed during 1053 cycles. Relevant patient informations were collected at the beginning of the first cycle and the number of days of FN were counted in the follow-up [dichotomized (no FN versus >or= 1 day of FN)]. RESULTS Aggressive chemotherapy regimen is the major predictor of FN [odds ratio 5.2 (3.2-8.4)]. The other independent predictors are the underlying disease, an involvement of bone marrow, body surface <or= 2 m(2), a baseline monocyte count <150/microl and the interaction between the first cycle in the same treatment line and a baseline hemoglobin dosage. A rule of prediction of FN was computed with these characteristics: sensitivity 78.6%, specificity 62.3%, positive predictive value 42.7% and negative predictive value 89.1%. CONCLUSION Further studies are needed to validate this score.


Supportive Care in Cancer | 2006

Causes of fever in cancer patients (prospective study over 477 episodes).

Emmanuel Toussaint; E. Bahel-Ball; Marc Vekemans; Aspasia Georgala; L. Al-Hakak; Marianne Paesmans; Michel Aoun

Goals of workThe aim of this study was to determine the causes of fever among cancer patients.MethodsAll febrile cancer patients were followed up prospectively. Clinical, microbiological and radiological documentations were performed. Aetiologies of fever, type of tumour, site of infection, type of microorganism and outcome were assessed and compared between neutropenics and non-neutropenics.ResultsFour hundred and seventy-seven episodes were evaluated. Infection, non-infectious causes and fever of unknown origin represented 67, 23 and 10%, respectively. The respiratory tract is the most frequently involved site in infection (29%), and in microbiologically documented infections, Gram-negative bacilli were predominant. The tumour itself (27%) or an invasive procedure (17%) were the main causes of non-infectious febrile episodes. Mortality from infection was higher among non-neutropenic (11.1%) than neutropenic patients (4.3%).ConclusionFever in cancer patients remains a challenge, and the differentiation between infectious and non-infectious causes at onset of fever is very difficult. Despite all the prophylactic measures, infection is still the principal cause. However, the infection-related mortality is low either in neutropenic or non-neutropenic patients.


The Journal of Infectious Diseases | 2013

Heterogeneity and Evolution of Thymidine Kinase and DNA Polymerase Mutants of Herpes Simplex Virus Type 1: Implications for Antiviral Therapy

Graciela Andrei; Aspasia Georgala; Dimitrios Topalis; Pierre Fiten; Michel Aoun; Ghislain Opdenakker; Robert Snoeck

BACKGROUND Infections caused by acyclovir-resistant isolates of herpes simplex virus (HSV) after hematopoietic stem cell transplantation (HSCT) are an emerging concern. An understanding of the evolutionary aspects of HSV infection is crucial to the design of effective therapeutic and control strategies. METHODS Eight sequential HSV-1 isolates were recovered from an HSCT patient who suffered from recurrent herpetic gingivostomatitis and was treated alternatively with acyclovir, ganciclovir, and foscavir. The diverse spectra and temporal changes of HSV drug resistance were determined phenotypically (drug-resistance profiling) and genotypically (sequencing of the viral thymidine kinase and DNA polymerase genes). RESULTS Analysis of 60 clones recovered from the different isolates demonstrated that most of these isolates were heterogeneous mixtures of variants, indicating the simultaneous infection with different drug-resistant viruses. The phenotype/genotype of several clones associated with resistance to acyclovir and/or foscavir were identified. Two novel mutations (E798K and I922T) in the viral DNA polymerase could be linked to drug resistance. CONCLUSIONS The heterogeneity within the viral populations and the temporal changes of drug-resistant viruses found in this HSCT recipient were remarkable, showing a rapid evolution of HSV-1. Drug-resistance surveillance is highly recommended among immunocompromised patients to manage the clinical syndrome and to avoid the emergence of multidrug-resistant isolates.


Supportive Care in Cancer | 2011

Predicting febrile neutropenic patients at low risk using the MASCC score: does bacteremia matter?

Marianne Paesmans; Jean Klastersky; Johan Maertens; Aspasia Georgala; Frédérique Muanza; Michel Aoun; Augustin Ferrant; Bernardo Rapoport; Kenneth V. I. Rolston; Lieveke Ameye

BackgroundFebrile neutropenic cancer patients represent a heterogeneous population with a limited proportion at risk of serious medical complications. The Multinational Association for Supportive Care in Cancer (MASCC) score has been developed and validated for identifying low-risk patients at the onset of febrile neutropenia. Since bacteremia, although not documented at baseline, is a predictor of pejorative outcome, the purpose of this study was to investigate the possible interaction between the MASCC score and bacteremic status and to assess whether, assuming that bacteremic status could be predicted at onset of febrile neutropenia, adding bacteremia as a covariate in a risk model would improve the accuracy of low-risk patients identification.MethodsTwo consecutive multicentric observational studies were carried out from 1994 till 2005 involving 2,142 febrile neutropenic patients. The study data bases were retrospectively used for the present analysis.ResultsA predictive value was found for the MASCC score in all strata obtained by stratification for the bacteremic status with odds ratios for successful outcome being, in patients with a score ≥21, respectively, 6.06 (95%CI: 4.51–8.15), 3.42 (95%CI: 1.95–5.98), and 6.04 (95%CI: 3.01–12.09) in patients without bacteremia, gram-positive bacteremia, and gram-negative bacteremia. No interaction between the MASCC score and the bacteremic status was present. A clinical prediction rule integrating the MASCC score and the bacteremic status was not helpful in improving the identification of low-risk patients. This rule may then be used in a general population of patients with febrile neutropenia without having concerns for a lower predictive value in bacteremic patients.ConclusionsOur results suggest that the knowledge, provided we could find a model to predict it at fever onset, of a bacteremic etiology of the fever would be of little additional value to the MASCC score when attempting to identify low-risk patients.


Postgraduate Medical Journal | 2008

Non-Hodgkin’s lymphoma and tuberculosis coexistence in the same organs: a report of two cases

Panagiotis Fanourgiakis; Eleni Mylona; I I Androulakis; C Eftychiou; Evangelos Vryonis; Aspasia Georgala; Athanasios T. Skoutelis; Michel Aoun

Non-Hodgkin’s lymphoma (NHL) may be preceded by chronic inflammatory diseases and furthermore has been related to immune deficiency. Tuberculosis (TB), on the other hand, is a chronic infectious disease whose presentation and reactivation is known to be promoted by cell mediated immunodeficiency. The coexistence of NHL and TB in the same organ is rare. We report two cases of NHL and TB coexistence in two different organs: cervical lymph nodes and kidney. The cases illustrate how misleading the concurrence of NHL and TB infection can be, delaying the diagnosis and treatment of either disease.


Mycoses | 2011

Inaugural bilateral aspergillus endophthalmitis in a seriously immunocompromised patient

Aspasia Georgala; B Layeux; John Kwan; Irshad Ahmad; Jacques Libert; Francois Willermain; Philippe Koch; Corine Heymans; M. Husson; Michel Aoun

A. Georgala, B. Layeux, J. Kwan, I. Ahmad, J. Libert, F. Willermain, P. Koch, C. Heymans, M. Husson and M. Aoun Department of Internal Medicine – CHU Brugmann, Bruxelles, Belgium, Department of Clinical Oncology, Institut Jules Bordet, Université Libre de Bruxelles, Belgium, Department of Haematology, Institut Jules Bordet, Université Libre de Bruxelles, Belgium, Microbiology Laboratory ⁄ Section of Mycology, Institut Jules Bordet, Université Libre de Bruxelles, Belgium, Department of Ophthalmology, CHU-St Pierre, Bruxelles, Belgium and Department of Infectious Diseases, Institut Jules Bordet, Université Libre de Bruxelles, Belgium


Expert Review of Hematology | 2015

Prophylaxis of febrile neutropenia in adults receiving chemotherapy needs to be adapted to the risk

Aspasia Georgala; Jean Klastersky

A major advance in the management of febrile neutropenia (FN) has been the stratification of the population of adult patients with FN for the risk of complications and death. Using validated reliable predictive instruments, such as the Multinational Association for Supportive Care in Cancer score, it is possible to identify a population of ‘low-risk’ patients, who can benefit from simplified and less expensive therapeutic approaches (e.g., orally administered antimicrobial therapy and early home return). Prevention of FN by the use of granulopoietic colony-stimulating factor (G-CSF) has been successfully applied to patients at ‘high risk’ of developing FN. In addition to the aggressiveness of chemotherapy, which usually defines the ‘high-risk’ status, the role of a series of factors that increase both the risk of FN and the complications rate has been recognized and should probably be taken into consideration when selecting patients for G-CSF prophylaxis. The cost of the G-CSF is the major limiting factor for their broad use; further efforts should be made to match the cost issue with the need of protecting from the development of FN most patients treated with chemotherapy for cancer.

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Jean Klastersky

Université libre de Bruxelles

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Marianne Paesmans

Université libre de Bruxelles

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Ahmad Awada

Université libre de Bruxelles

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Augustin Ferrant

Cliniques Universitaires Saint-Luc

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