Cytomegalovirus DNAemia and disease: current-era epidemiology, clinical characteristics and outcomes in cancer patients other than allogeneic haemopoietic transplantation
Details
Publication Year 2022-10,Volume 52,Issue #10,Page 1759-1767
Journal Title
Internal Medicine Journal
Publication Type
Research article
Abstract
BACKGROUND: High-intensity chemotherapy and advances in novel immunotherapies have seen the emergence of cytomegalovirus (CMV) infections in cancer patients other than allogeneic haemopoietic cell transplantation (HCT). Aim To evaluate the epidemiology, clinical characteristics and outcomes of CMV infection in this population. METHODS: A retrospective review of cancer patients other than allogeneic HCT who had CMV DNAemia and/or disease from July 2013 till May 2020 at a quaternary cancer centre was performed. RESULTS: Of 11 485 cancer patients who underwent treatment during this period, 953 patients had CMV DNA testing performed and 238 of them had CMV DNAemia. After excluding patients with allogeneic HCT, 62 patients with CMV DNAemia were identified, of whom 10 had concurrent CMV disease. The most frequent underlying malignancies were B-cell lymphoproliferative disease (LPD) (31%; 19/62), T-cell LPD (21%; 13/62), chronic lymphocytic leukaemia (11%; 7/62) and multiple myeloma (10%; 6/62). Most patients had lymphopenia (77%; 48/62), multiple cancer therapies (63%; 39/62 received >/=2 previous therapies), co-infection (56%; 35/62 had >/=1 co-infection) and corticosteroid therapy (48%; 30/62) within 1 month before CMV diagnosis. CMV DNAemia and disease were observed in patients receiving novel immunotherapies, including bispecific antibody therapy, chimeric-antigen receptor T-cell therapy and immune checkpoint inhibitors. CONCLUSION: Patients with haematological malignancy, particularly B-cell LPD, T-cell LPD, chronic lymphocytic leukaemia and multiple myeloma, were frequently identified to have CMV DNAemia and disease. Lymphopenia, multiple cancer therapies, co-infection and recent receipt of systemic corticosteroids were also commonly observed. Future studies are necessary to determine optimal identification and management of CMV in these patients.
Publisher
Wiley
Keywords
Humans; Cytomegalovirus/genetics; *Multiple Myeloma; *Leukemia, Lymphocytic, Chronic, B-Cell; *Coinfection; Immune Checkpoint Inhibitors; DNA, Viral; *Cytomegalovirus Infections/diagnosis/epidemiology; *Hematopoietic Stem Cell Transplantation/adverse effects; *Lymphopenia/etiology; Receptors, Antigen; Adrenal Cortex Hormones; CMV DNAemia; CMV end-organ disease; haematological malignancy; immunotherapy; non-allogeneic transplantation
Department(s)
Infectious Diseases; Health Services Research; Haematology
PubMed ID
34448333
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