#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

Infectious complications of induction therapy in acute myeloid leukaemia patients without the use of antibiotic prophylaxis


Authors: M. Čerňan 1;  T. Szotkowski 1;  M. Kolář 2;  J. Hubáček 1;  E. Faber 1
Authors‘ workplace: Hemato-onkologická klinika LF UP a FN Olomouc 1;  Ústav mikrobiologie LF UP a FN Olomouc 2
Published in: Transfuze Hematol. dnes,21, 2015, No. 1, p. 14-23.
Category: Comprehensive Reports, Original Papers, Case Reports

Overview

The induction chemotherapy represents one of the riskiest phases of therapy of acute myeloid leukaemia (AML) due to reduced haematopoiesis and a big tumour mass. Therefore, the infectious complications are very frequent in patients undergoing induction chemotherapy. They represent an important risk factor of the mortality of primary diagnosis. This research aims at describing the infectious complications and their therapy carried out during the first cycle of induction chemotherapy on the group of 100 AML patients, who were treated without antibiotic prophylaxis, in the Department of Haemato-Oncology, Faculty of Medicine and Dentistry, Palacký University and University Hospital Olomouc during the years 2007–2011. This research also compares the result of the above patient group with the groups of AML patients published in literature who had been given an antibiotic prophylaxis during induction. Our results showed that 93% of patients had infectious complications during induction chemotherapy. Clinically and/or microbiologically documented infections were described in 48 patients and febrile neutropenia was described in 45 patients. Sepsis was documented in 32 patients, inflammatory infiltrate of lungs and extrapulmonary infectious focuses were observed in 24 patients each. Proven invasive fungal infections were noticed in 2, probable in 4 and possible in 29 patients. The achieving of complete remission (67%) after induction therapy had a significant influence on lower occurrence of sepsis (22.4% vs. 51.5%, p = 0.0037), shorter hospitalization (35.1 vs. 39.4 days, p = 0.028), shorter antibiotic (27.8 vs. 35.0 days, p = 0.011) and antifungal (27.9 vs. 33.2 days, p = 0.031) therapy in comparison with non-remission patients. Seven patients undergoing induction chemotherapy had no signs of infection. Infectious complications were the cause of death in 3 patients. The results showed that, occurrence of infectious complications during induction was not significantly higher in patients without the use of antibiotic prophylaxis in comparison with published data of patients receiving antibiotic prophylaxis (93.0% vs. 85.2% (p = 0.088), respectively 91.3% (p = 0.58). The monitoring of bacterial resistance, adverse effects and clinical efficiency should be the conditions for using antibiotic prophylaxis in patients undergoing induction chemotherapy for AML.

Key words:
acute myeloid leukaemia, induction chemotherapy, infectious complications, complete remission


Sources

1. Szotkowski T, Faber E. Akutní leukemie. In: Faber E, et al. Základy hematologické diagnostiky. Univerzita Palackého v Olomouci, 2012, ISBN 978-80-244-2935-9, s. 153–159.

2. Trněný M, Čermák J, Klamová H, et al. Akutní myeloidní leukemie. In Češka R, et al. Interna. Triton, 2010, ISBN 978-80-7387-423-0, s. 684–686.

3. Bodey GP, Buckley M, Sathe YS, Freireich EJ. Quantitative relationships between circulating leukocytes and infection in patients with acute leukemia. Ann Intern Med 1966; 64(2): 328–340.

4. Drgoňa Ľ. Febrilná neutropénia. In Drgoňa Ľ. Infekčné komplikácie onkologických pacientov - vybrané kapitoly. Univerzita Komenského v Bratislave, 2013, ISBN 978-80-223-3468-6, s. 10–22.

5. Sanz AM, Montesinos P, Vellanga E, et al. Risk-adapted treatment of acute promyelocytic leukemia with all-trans retinoic acid and anthracycline monochemotherapy: long-term outcome of the LPA 99 multicenter study by the PETHEMA Group. Blood 2008; 112(8): 3130–3134.

6. Tallman MS, Gilliland DG, Rowe JM. Drug therapy for acute myeloid leukemia. Blood 2005; 106: 1154–1163.

7. Dillman RO, Davis RB, Green MR, et al. A comparative study of two different doses of cytarabine for acute myeloid leukemia: a phase III trial of Cancer and Leukemia Group B. Blood 1991; 78: 2520–2526.

8. Ascioglu S, Rex JH, Pauwde B, et al. Defining Opportunistic Invasive Fungal Infections in Immunocompromised Patients with Cancer and Hematopoietic Stem Cell Transplants: An International Consensus. Clin Infect Dis 2002; 34(1): 7–14.

9. Sherif F, Brahm H. Pľúcna aspergilóza – klinické prejavy, diagnostika, liečba a komplikácie. Curr Opin Pulm Med/CS 2010; 7: 31–38.

10. Drgoňa Ľ. Febrilná neutropénia. Onkológia (Bratisl.) 2012; 7(1): 20–23.

11. De Rosa FG, Motta I, Audisio E, et al. Epidemiology of bloodstream infections in patients with acute myeloid leukemia undergoing levofloxacin prophylaxis. BMC Infectious Diseases 2013; 13: 563.

12. Malagola M, Peli A, Damiani D, et al. Incidence of bacterial and fungal infections in newly diagnosed acute myeloid leukaemia patients younger than 65 yr treated with induction regimens including fludarabine: retrospective analysis of 224 cases. Eur J Haematol 2008; 81(5): 354–363.

13. Lech-Maranda E, Seweryn M, Giebel S, et al. Infectious complications in patients with acute myeloid leukemia treated according to the protocol with daunorubicin and cytarabine with or withoutaddition of cladribine. A multicenter study by the Polish Adult Leukemia Group (PALG). International Journal of Infectious Diseases 2010; 14: 132–140.

14. Kinnunen U, Koistinen P, Ohtonen P, Koskela M, Syrjälä H. Influence of chemotherapy courses on the rate of bloodstream infections during neutropenia in adult acute myeloid leukaemia. Scandinavian Journal of Infectious Diseases 2008; 40: 642–647.

15. Gupta A, Singh M, Singh H, et al. Infections in acute myeloid leukemia: an analysis of 382 febrile episodes. Med Oncol 2010; 27: 1037–1045.

16. Syrjälä H, Ohtonen P, Kinnunen U, et al. Blood stream infections during chemotherapy-induced neutropenia in adult patients with acute myeloid leukemia: treatment cycle matters. Eur J Clin Microbiol Infect Dis 2010; 29: 1211–1218.

17. Gafter-Gvili A, Fraser A, Paul M, et al. Antibiotic prophylaxis for bacterial infections in afebrile neutropenic patients following chemotherapy. Cochrane Database Syst Rev 2012; 1: CD004386.

18. Bucaneve G, Castagnola E, Viscoli C, Leibovici L, Menichetti F. Quinolone prophylaxis for bacterial infections in afebrile high risk neutropenic patients. EJC supplements 2007; 5: 5–12.

19. Haber J, Cetkovský P, Ráčil Z, et al. Antibiotická profylaxe u hematologických nemocných – doporučení odborníků s podporou CELL, ČHS a ČOS ČLS JEP, S.CH.S. SLS. Postgraduální medicína 2011; 13(5): 43–46.

20. Shilpan SS, Kantarjian H, Farhad R, O’Brien S, Garcia-Menero G, Andreeff M. Survival Outcomes In Relapsed/Refractory Acute Myeloid Leukemia Patients Who Achieve Less-Than-Complete Response After Salvage Therapy. Blood 2013; 122(21): 2654.

Labels
Haematology Internal medicine Clinical oncology

Article was published in

Transfusion and Haematology Today

Issue 1

2015 Issue 1

Most read in this issue
Login
Forgotten password

Enter the email address that you registered with. We will send you instructions on how to set a new password.

Login

Don‘t have an account?  Create new account

#ADS_BOTTOM_SCRIPTS#