Invasive Fungal Diseases Impact On Outcome of Childhood ALL – An Analysis of the International Trial AIEOP-BFM ALL 2009

Author:

Lehrnbecher Thomas1,Groll Andreas2ORCID,Cesaro Simone3ORCID,Alten Julia4,Attarbaschi Andishe5,Barbaric Draga6,Bodmer Nicole7,Conter Valentino8,Izraeli Shai9ORCID,Mann Georg5,Moericke Anja10,Niggli Felix11,Schrappe Martin10,Stary Jan12,Zapotocka Ester13,Zimmermann Martin14,Elitzur Sarah15ORCID

Affiliation:

1. University of Frankfurt

2. University Children's Hospital Muenster

3. Ospedale Donna Bambino

4. Berlin-Frankfurt-Münster Group Germany (BFM-G; Germany, Switzerland)

5. St. Anna Children's Hospital

6. Sydney Children’s Hospital

7. University Children's Hospital Zürich

8. Ospedale San Gerardo

9. Schneider Children's Medical Center

10. University Hospital Schleswig-Holstein, Campus Kiel

11. University Children's Hospital Zurich

12. University Hospital Motol and 2nd Medical School, Charles University Prague

13. University Hospital Motol

14. Hannover Medical School

15. Schneider Children's Medical Center, Sackler School of Medicine, Tel-Aviv University

Abstract

Abstract In children with acute lymphoblastic leukemia (ALL), risk groups for invasive fungal disease (IFD) with need for antifungal prophylaxis are not well characterized, and with the advent of new antifungal compounds, current data on outcome are scarce. Prospectively captured severe adverse event reports of children enrolled in the international, multi-center clinical trial AIEOP-BFM ALL2009 were screened for proven/probable IFD, defined according to the updated EORTC/MSG consensus definitions. In a total of 6136 children (median age 5.2 years), 224 proven/probable IFDs (65 yeast and 159 mold) were reported. By logistic regression, the risk for proven/probable IFDs was significantly increased in children ≥ 12 years and those with a blast count ≥ 10% in the bone marrow on day 15 (P < 0.0001 each). Proven/probable IFDs had a 6-week and 12-week mortality of 10.7% and 11.2%, respectively. In the multivariate analysis, the hazard ratio for event-free and overall survival was significantly increased for proven/probable IFD, age ≥ 12 years, and insufficient response to therapy (P < 0.001, each). Our data define older children with ALL and those with insufficient treatment-response at high risk for IFD. As we show that IFD is an independent risk factor for event-free and overall survival, these patients may benefit from targeted antifungal prophylaxis.

Publisher

Research Square Platform LLC

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