
 
		ANTIMICROBIAL PROPHYLAXIS WITH LEVOFLOXACIN IS NOT EFFECTIVE IN PREVENTING  
 FEBRILE NEUTROPENIA IN ACUTE MYELOID LEUKEMIA AND HIGH-RISK MYELODISPLASTIC  
 POSTER 14  
 SYNDROME PATIENTS TREATED WITH HYPOMETHYLATING AGENTS :   
 A SINGLE CENTRE EXPERIENCE.  
    
 Alessandro Fiorentini1,  Debora Capelli1,  Alberto Carturan1,  Erika Morsia1,  Diego Menotti1 and  
 Massimo Offidani2, Attilio Olivieri1  
   
 (1)OspedaliRiunitiAncona, Ancona, Italy   
 (2)OspedaliRiuniti, Ancona, Italy  
    
 Objectives : To date, the role of prophylactic antibacterial agents in Acute Myeloid Leukemia (AML)  
 and High-Risk Myelodisplastic  Syndrome  (HR-MDS)  patients  undergoing treatment with  
 hypomethylating agents  (HMAs)  remains controversial and there  are no clinical guidelines  for  
 infection prophylaxis in these clinical settings The aim of this study is to retrospectively analyze the  
 effect of antimicrobial prophylaxis with levofloxacin (500 mg/die) on incidence of febrile neutropenia  
 (FN) in AML and MDS patients treated with HMAs.  
 Methods : We  retrospectively analyzed the incidence  of FN according to  EORTC  criteria in 129  
 consecutive AML (n=93) and MDS (n=36) patients (median age 73, range 22-86) receiving a total of  
 1430 courses of HMAs (1145 cycles of 5-azacytidine , 285 cycles of decitabine, range 1–68) between  
 September 2011 and December 2019 at our institute. Cumulative risk of FN was estimated using the  
 Kaplan-Meier method and the differences between curves evaluated using a log-rank test. Age, type  
 of haematologic  malignacy,  ECOG  performance  status, transfusion  indipendence,  type  of HMA,  
 HB/PLT/WBC/ANC levels at baseline, presence of BPCO, diabetes, prior or concomitant corticosteroid  
 therapy, use  of G-CSF and antimicrobial prophylaxis were used  as stratification factors  in the  Cox  
 regression model to estimate the hazard ratio.  
 Results: One hundred-twenty-one cases  of  FN occurred in this series,  with 79 cases requiring  
 hospitalization. The incidence rate of FN was 9 % per treatment cycle. The cumulative risk of FN was  
 significantly higher in the cohort  assuming antimicrobial phrophylaxis (p<0,01 ; Table 1). ECOG > 2  
 (hazard ratio (HR)  13.41;  p <  .001)  , ANC  levels  <500/mmc (HR  8,6; p 0,003),  and antimicrobic  
 prophylaxis (HR 10.35; p = 0,001) were significant for development of FN at Cox regression analysis.  
 Conclusions : Based on these limited data, antimicrobial prophylaxis with levofloxacin is not effective  
 in preventing  febrile neutropenia in AML/MDS patients  treated with hypomethylating  agents. This  
 result  may be  explained by  the potential  selective  pressure  carried  out by the continuous  
 antimicrobial therapy and the emergence of multi-drug resistant bacteria.  
 SCIENTIFIC  
 PROGRAMME 
 RARE SUBSETS OF  
 ACUTE LEUKAEMIA 
 TRACKING LEUKAEMIC  
 STEM CELLS (LSCs) 
 ROUTINE DIAGNOSIS  
 GENE EXPRESSION  
 AND MUTATIONAL  
 PROFILING 
 DEBATE 1 – ALL  
 PATIENTS WITH  
 INTERMEDIATE-RISK  
 AML MUST BE  
 TRANSPLANTED 
 INTERACTIVE   
 CASES 1 – MUTATION-BASED  
 THERAPY   
 OFF-LABEL 
 ROUNDTABLE –  
 SHOULD WE REALLY  
 USE NEW TARGETED  
 INHIBITORS AS SINGLE  
 AGENTS ? 
 ADDITION OF A 3RD  
 AGENT TO FRONTLINE  
 7+3 
 ROUNDTABLE –  
 CURATIVE OPTIONS  
 FOR OLDER AML 
 INTERACTIVE CASES 2 
 DEBATE 2 - BEST  
 TREATMENT FOR  
 NPM1-MUTATED AML IN  
 THE NEXT FUTURE ? 
 ALLOGENEIC  
 HAEMATOPOIETIC  
 STEM CELL  
 TRANSPLANTATION  
 (HSCT) 
 IMMUNOTHERAPY FOR  
 ACUTE LEUKAEMIA 
 DEBATE 3 - T-ALL:  
 WHERE ARE WE GOING  
 NOW? 
 SELECTED ABSTRACTS  
 AND CLINICAL  
 CASES FOR AN ORAL  
 PRESENTATION 
 SELECTED ABSTRACTS  
 FOR A POSTER  
 PRESENTATION 
 DISCLOSURES