27.12.2012 Views

12th Congress of the European Hematology ... - Haematologica

12th Congress of the European Hematology ... - Haematologica

12th Congress of the European Hematology ... - Haematologica

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

12 th <strong>Congress</strong> <strong>of</strong> <strong>the</strong> <strong>European</strong> <strong>Hematology</strong> Association<br />

75%, induction for acute leukemia - 50%, consolidation for acute<br />

leukemia - 33%, autologous HSCT - 10%, o<strong>the</strong>r treatment for miscellaneous<br />

hematological malignancies - 33%. Summary and conclusions. GM<br />

detection by Platelia Aspergillus kit is very useful for diagnosis <strong>of</strong> IA in<br />

hematooncological pts. The test has very high sensitivity and especially<br />

very high NPV and so negative test result can exclude IA. The main<br />

problem <strong>of</strong> <strong>the</strong> test is false positivities, especially common in group <strong>of</strong><br />

hematological pts. with low prevalence <strong>of</strong> IA. Therefore <strong>the</strong> regular<br />

screening for GM should be performed only in pts. groups were prevalence<br />

<strong>of</strong> IA is high - pts undergoing allogeneic HSCT or treatment for<br />

acute leukemia. In low risk group <strong>the</strong> test should be performed only<br />

when <strong>the</strong>re is clinical suspicion <strong>of</strong> invasive fungal infection and positive<br />

result should be interpreted very carefully to avoid overtreatment with<br />

expensive new antifungals.<br />

This work was supported by grant <strong>of</strong> Ministry <strong>of</strong> Health <strong>of</strong> <strong>the</strong> Czech Republic<br />

(IGA NR8452-3/2005).<br />

0209<br />

INCIDENCE OF INVASIVE ASPERGILLOSIS IN ALLOGENEIC STEM CELL<br />

TRANSPLANTATION RECIPIENTS: AN ITALIAN PROSPECTIVE MULTICENTER STUDY<br />

N. Mordini, 1 D. Mattei, 1 B. Bruno, 2 A. Busca, 3 B. Allione, 4 F. Carnevale<br />

Schianca, 5 R. Sorasio, 2 A. Davit, 1 M. Rotta, 2 D. Rapezzi, 1<br />

M. Boccadoro, 2 A. Levis, 4 M. Aglietta, 5 E. Gallo, 3 A. Gallamini1 1 ASO S.Croce e Carle, CUNEO; 2 University <strong>of</strong> Turin, TURIN; 3 S.Giovanni<br />

Battista Hospital, TURIN; 4 SS. Antonio e Biagio Hospital, ALESSANDRIA;<br />

5 IRCC, CANDIOLO, Italy<br />

Background. So far only retrospective studies have been published<br />

focusing on <strong>the</strong> incidence <strong>of</strong> Invasive Aspergillosis (IA) in allogeneic<br />

hematopoietic stem cell transplantation (alloSCT). Patients and Methods.<br />

Between December 2003 and October 2005, 206 patients admitted to<br />

four Piedmont Hematological institutions, on behalf <strong>of</strong> vita vitae project.<br />

Patients, accounting for 217 alloSCT, were consecutive enrolled in <strong>the</strong><br />

trial on <strong>the</strong> role <strong>of</strong> combined intensive screening for circulating galactomannan<br />

(GM) and early high resolution chest CT (HRCT) for IA diagnosis.<br />

GM sampling were collected twice in a week from admittance<br />

until day +365; HRCT and/or bronchoscopy with bronco-alveolar lavage<br />

(BAL) were performed when IA was suspected. AlloSCT were performed<br />

for: Multiple Myeloma (61), Lymphoma (39), Acute Leukemia<br />

(64), Myeloprolipherative Disorders (15), Severe Aplastic anemia (2),<br />

solid tumor (14 ) and Chronic Lymphocytic Leukemia (8). Donors were<br />

HLA-Identical siblings (179) or alternative (38). Stem cell source was<br />

peripheral (190), cord blood (2) and bone marrow(15). Conditioning was<br />

myeloablative (104) or Reduced-intensity (113). Previous autologous<br />

SCT was done in 82 patients. One-hundred-fifty-five patients underwent<br />

alloSCT in PR and 72 in CR. Acute and chronic Graft versus Host<br />

Disease (GvHD) affected 157 alloSCTs. Only proven and probable IA,<br />

diagnosed according to <strong>the</strong> EORTC/MSG criteria were considered for<br />

<strong>the</strong> analysis <strong>of</strong> IA incidence. Results. With a follow-up range <strong>of</strong> 12 to 34<br />

months, 115 patient were alive and 91 had died. Relapse accounted for<br />

57 deaths, transplant related mortality (TRM) for 58, including 10 due<br />

to IA Twenty-five cases <strong>of</strong> IA were diagnosed: 2 proven and 23 probable.<br />

Six cases were classified as early IA (within day +40 from SCT) and<br />

19 as late IA (beyond day +40 to one year), with an overall incidence <strong>of</strong><br />

11,5%. Neutropenia

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!