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E-Poster Display

907P - Invasive aspergillosis caused by aspergillus non-fumigatus in children and adults after hematopoietic stem cell transplantation (HSCT) & chemotherapy

Date

17 Sep 2020

Session

E-Poster Display

Topics

Cytotoxic Therapy

Tumour Site

Haematological Malignancies

Presenters

Yuliya Rogacheva

Citation

Annals of Oncology (2020) 31 (suppl_4): S590-S598. 10.1016/annonc/annonc261

Authors

Y. Rogacheva1, M. Popova2, A. Siniaev1, A. Volkova1, I. Markova1, I. Nikolaev1, O. Pinegina1, S. Ignatieva3, T. Bogomolova3, A. Gevorgayn1, O. Paina1, T. Bykova1, Y. Vlasova1, O. Goloshchapov1, M. Vladovskaya1, S. Bondarenko1, N. Klimko3, L. Zubarovskaya1

Author affiliations

  • 1 Hematology, Raisa Gorbacheva Memorial Institute of Children Oncology, Hematology and Transplantation, First Pavlov State Medical University of Saint-Petersburg, 197022 - Санкт-Петербург/RU
  • 2 Hematology, Raisa Gorbacheva Memorial Institute of Children Oncology, Hematology and Transplantation, First Pavlov State Medical University of Saint-Petersburg, 197022 - Saint Petersburg/RU
  • 3 Mycology, I.I. Mechnikov North-Western State Medical University, Ministry of Health of Russia, 197022 - Санкт-Петербург/RU

Resources

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Abstract 907P

Background

Aspergillus fumigatus is the most common etiologic agent of invasive aspergillosis (IA) reported in severely immunocompromised patients. Aspergillosis caused by non-fumigatus Aspergillus species is poorly studied.

Methods

We design the retrospective study in order to investigate the epidemiology of IA caused by Aspergillus non-fumigatus as a single agent in large cohort of patients after HSCT and chemotherapy from 2013 to 2018 in CIC725. During the observation period 30 patients with IA caused by Aspergillus non-fumigatus were identified and included into analysis. The median age was 26 (3-60) y.o., males – 53%. The median follow up time was 10 months; for survivors – 17,5 months.

Results

A. non-fumigatus IA was more common diagnosed in allo-HSCT recipients (90%) then after chemotherapy (10%). Most of the patients at the moment of IA diagnosed received antifungal prophylaxis with fluconazole (83%) or echinocandins (6,7%). Breakthrough IA (prophylaxis with voriconazole – 2, posaconazole – 1) was diagnosed in 10% of patients. Etiology agents were Aspergillus niger – 60%, A. flavus – 34%, A. glaucus – 3%, and A. terreus – 3%. The main sites of infection were lungs (80%), paranasal sinuses (10%), or combination lungs and paranasal sinuses (10%). A. non-fumigatus IA developed in combination with bacterial or other fungal infections in 20% (n=6). The median time of onset of A. non-fumigatus IA after allo-HSCT was 155 (19-922) days. Antifungal therapy was used in all patients: voriconazole – 73,3%, lipid amphotericin B – 6,7%, posaconazole – 6,7%, combination therapy – 13,3%. A. non-fumigatus IA developed on the background of acute graft-versus-host diseases (GVHD) grade 2-3 + glucocorticoids therapy (25%) and CMV reactivation (19%). Overall survival at 12 weeks from the diagnosis of A. non-fumigatus IA was 83,3%. Death could be attributed to IA was registered in one case.

Conclusions

Aspergillus non-fumigatus IA affected allo-HSCT recipients (90%). Aspergillus niger was the main etiology agent. Aspergillus non-fumigatus IA was a late complication and developed on the background of CMV reactivation and acute GVHD. Overall survival at 12 weeks from the IA diagnosis was 83,3%.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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