Risk Factors, Prevalence, and Outcomes of Invasive Fungal Disease Post Hematopoietic Cell Transplantation and Cellular Therapies: A Retrospective Monocenter Real-Life Analysis

Author:

Gavriilaki Eleni12ORCID,Dolgyras Panagiotis1ORCID,Dimou-Mpesikli Sotiria1,Poulopoulou Aikaterini3,Evangelidis Paschalis2ORCID,Evangelidis Nikolaos2ORCID,Demosthenous Christos1,Zachrou Evangelia3,Siasios Panagiotis3ORCID,Mallouri Despina1,Vardi Anna1,Bousiou Zoi1ORCID,Panteliadou Alkistis1,Batsis Ioannis1,Masmanidou Marianna1,Lalayanni Chrysavgi1,Yannaki Evangelia1,Sotiropoulos Damianos1,Anagnostopoulos Achilles1ORCID,Vyzantiadis Timoleon-Achilleas3ORCID,Sakellari Ioanna1

Affiliation:

1. Bone Marrow Transplantation Unit, Haematology Department, G. Papanicolaou Hospital, 57010 Thessaloniki, Greece

2. Second Propedeutic Department of Internal Medicine, Hippocration Hospital, Aristotle University of Thessaloniki, 54642 Thessaloniki, Greece

3. Department of Microbiology, Medical School, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece

Abstract

(1) Background: Autologous, allogeneic hematopoietic cell transplantation (HCT) and other cellular therapies, including CAR T cell and gene therapy, constitute a cornerstone in the management of various benign and malignant hematological disorders. Invasive fungal infections (IFD) remain a significant cause of morbidity and mortality in HCT recipients. Therefore, we investigated the prevalence and risk factors of IFD following HCT and other cellular therapies in an era of novel antifungal prophylaxis. (2) Methods: In this study, we retrospectively enrolled adult HCT recipients who were treated at our JACIE-accredited center according to standard operating procedures over the last decade (2013–2022). (3) Results: 950 patients who received cellular therapies were studied. None of the 19 CAR T cell and neither of the two gene therapy recipients developed IFD whereas 3/456 autologous HCT recipients who suffered from primary refractory/relapsed lymphomas presented with probable IFD. Overall, 11 patients who received allogeneic HCT experienced probable IFD, possible IFD was found in 31/473, and IFD was proven in 10/473. A second IFD episode was present in three patients. Four-year OS was significantly lower in proven compared to probable IFD (p = 0.041) and was independently associated with HCT-CI (p = 0.040) and chronic GVHD (p = 0.045). (4) Conclusions: In this real-world cohort, the prevalence of proven and probable IFD in an era of novel antifungal prophylaxis was found to be relatively low. However, IFDs were associated with poor outcomes for patients who received allogeneic HCT.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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