Kai Rejeski1,2,3, Wolfgang G Kunz4, Martina Rudelius5, Veit Bücklein6,7, Viktoria Blumenberg6,7, Christian Schmidt6, Philipp Karschnia8, Florian Schöberl9, Konstantin Dimitriadis9, Louisa von Baumgarten9, Joachim Stemmler6, Oliver Weigert6, Martin Dreyling6, Michael von Bergwelt-Baildon6,10, Marion Subklewe6,7,10. 1. Department of Hematology and Oncology, University Hospital, LMU Munich, Munich, Germany. kai.rejeski@med.uni-muenchen.de. 2. Laboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany. kai.rejeski@med.uni-muenchen.de. 3. German Cancer Consortium (DKTK) and German Cancer Research Center, Heidelberg, Germany. kai.rejeski@med.uni-muenchen.de. 4. Department of Radiology, University Hospital, LMU Munich, Munich, Germany. 5. Department of Pathology, University Hospital, LMU Munich, Munich, Germany. 6. Department of Hematology and Oncology, University Hospital, LMU Munich, Munich, Germany. 7. Laboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany. 8. Department of Neurosurgery, University Hospital, LMU Munich, Munich, Germany. 9. Department of Neurology, University Hospital, LMU Munich, Munich, Germany. 10. German Cancer Consortium (DKTK) and German Cancer Research Center, Heidelberg, Germany.
Abstract
BACKGROUND: Prolonged myelosuppression following CD19-directed CAR T-cell transfusion represents an important, yet underreported, adverse event. The resulting neutropenia and multifactorial immunosuppression can facilitate severe infectious complications. CASE PRESENTATION: We describe the clinical course of a 59-year-old patient with relapsed/refractory DLBCL who received Axicabtagene-Ciloleucel (Axi-cel). The patient developed ASTCT grade I CRS and grade IV ICANS, necessitating admission to the neurological ICU and prolonged application of high-dose corticosteroids and other immunosuppressive agents. Importantly, neutropenia was profound (ANC < 100/μl), G-CSF-refractory, and prolonged, lasting more than 50 days. The patient developed severe septic shock 3 weeks after CAR transfusion while receiving anti-fungal prophylaxis with micafungin. His clinical status stabilized with broad anti-infective treatment and intensive supportive measures. An autologous stem cell backup was employed on day 46 to support hematopoietic recovery. Although the counts of the patient eventually started to recover, he developed an invasive pulmonary aspergillosis, which ultimately lead to respiratory failure and death. Postmortem examination revealed signs of Candida glabrata pancolitis. CONCLUSIONS: This case highlights the increased risk for fatal infectious complications in patients who present with profound and prolonged cytopenia after CAR T-cell therapy. We describe a rare case of C. glabrata pancolitis associated with multifactorial immunosuppression. Although our patient succumbed to a fatal fungal infection, autologous stem cell boost was able to spur hematopoiesis and may represent an important therapeutic strategy for DLBCL patients with CAR T-cell associated bone marrow aplasia who have underwent prior stem cell harvest.
BACKGROUND:Prolonged myelosuppression following CD19-directed CAR T-cell transfusion represents an important, yet underreported, adverse event. The resulting neutropenia and multifactorial immunosuppression can facilitate severe infectious complications. CASE PRESENTATION: We describe the clinical course of a 59-year-old patient with relapsed/refractory DLBCL who received Axicabtagene-Ciloleucel (Axi-cel). The patient developed ASTCT grade I CRS and grade IV ICANS, necessitating admission to the neurological ICU and prolonged application of high-dose corticosteroids and other immunosuppressive agents. Importantly, neutropenia was profound (ANC < 100/μl), G-CSF-refractory, and prolonged, lasting more than 50 days. The patient developed severe septic shock 3 weeks after CAR transfusion while receiving anti-fungal prophylaxis with micafungin. His clinical status stabilized with broad anti-infective treatment and intensive supportive measures. An autologous stem cell backup was employed on day 46 to support hematopoietic recovery. Although the counts of the patient eventually started to recover, he developed an invasive pulmonary aspergillosis, which ultimately lead to respiratory failure and death. Postmortem examination revealed signs of Candida glabrata pancolitis. CONCLUSIONS: This case highlights the increased risk for fatal infectious complications in patients who present with profound and prolonged cytopenia after CAR T-cell therapy. We describe a rare case of C. glabrata pancolitis associated with multifactorial immunosuppression. Although our patient succumbed to a fatal fungal infection, autologous stem cell boost was able to spur hematopoiesis and may represent an important therapeutic strategy for DLBCL patients with CAR T-cell associated bone marrow aplasia who have underwent prior stem cell harvest.
Entities:
Keywords:
CAR T-cell; Candida glabrata; Case report; Hematotoxicity; Invasive aspergillosis
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