TY - JOUR
T1 - Cytomegalovirus DNAemia and disease
T2 - current-era epidemiology, clinical characteristics and outcomes in cancer patients other than allogeneic haemopoietic transplantation
AU - Tay, Kim H.
AU - Slavin, Monica A.
AU - Thursky, Karin A.
AU - Coussement, Julien
AU - Worth, Leon J.
AU - Teh, Benjamin W.
AU - Khot, Amit
AU - Tam, Constantine S.
AU - Yong, Michelle K.
N1 - Funding Information:
We acknowledge the contributions of Ms Michelle Hong (Department of Pharmacy, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia) and Ms Marliese Alexander (Department of Pharmacy, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia) for providing pharmacy data, Ms Cathy Ma (Data Analyst, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia) and Mr Matthew Ha (Data Analyst, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia) for providing ICD-10 coding data and Mr Peter Gambell (Department of Pathology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia), Ms Cathy Carolan (Department of Pathology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia), Mr Josh Orth (Department of Pathology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia) and Dr Eloise Williams (Department of Microbiology, The Royal Melbourne Hospital, Melbourne, Victoria, Australia) for providing laboratory data.
Publisher Copyright:
© 2021 Royal Australasian College of Physicians.
PY - 2022/10
Y1 - 2022/10
N2 - 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.
AB - 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.
KW - CMV DNAemia
KW - CMV end-organ disease
KW - haematological malignancy
KW - immunotherapy
KW - non-allogeneic transplantation
UR - http://www.scopus.com/inward/record.url?scp=85118996122&partnerID=8YFLogxK
U2 - 10.1111/imj.15496
DO - 10.1111/imj.15496
M3 - Article
C2 - 34448333
AN - SCOPUS:85118996122
SN - 1444-0903
VL - 52
SP - 1759
EP - 1767
JO - Internal Medicine Journal
JF - Internal Medicine Journal
IS - 10
ER -