CMV Infection, Hematopoietic Stem Cell Transplantation
Conditions
Brief summary
Cytomegalovirus (CMV) remains a significant cause of morbidity and mortality after hematopoietic stem cell transplantation (HSCT). The course and outcome of CMV infection are different clinically, and the mechanism of CMV infection after transplantation has not been clarified. Reconstitution of cellular immunity after HSCT is a critical determinant of the control of CMV infection. Investigators will dynamically monitor the CMV-specific cellular immune reconstitution after HSCT，and analyze the clinical factors and therapy strategies affecting recovery of CMV-specific immunity during 1 year after HSCT.
Detailed description
Cytomegalovirus (CMV) remains a significant cause of morbidity and mortality after hematopoietic stem cell transplantation (HSCT). The course and outcome of CMV infection are different clinically, and the mechanism of CMV infection after transplantation has not been clarified. Reconstitution of cellular immunity after HSCT is a critical determinant of the control of CMV infection. Investigators will collect peripheral blood at 1 month, 2 month, 3 month, and 6 month after HSCT from the participated patients, and dynamically monitor the CMV-specific T and NK cellular immune reconstitution. Investigators will also analyze the clinical factors and therapy strategies affecting recovery of CMV-specific immunity during 1 year after HSCT.
Interventions
DRUGLetermovir
Patients received letermovir as prophylaxis or received preemptive therapy for CMV depends on clinical needs and patients' wishes
Sponsors
Peking University People's Hospital
Study design
Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
14 Years to 75 Years
Healthy volunteers
Yes
Inclusion criteria
* Be receiving a first allogeneic HSCT. * Is male or female, from 14 years to any years of age inclusive. * The participant (or legally acceptable representative) agree for cellular immune investigation and has provided documented informed consent/assent for the study.
Exclusion criteria
* Received a previous allogeneic HSCT (Note: Receipt of a previous autologous HSCT is acceptable). * Has a history of CMV end-organ disease within 6 months prior to allocation. * Has severe organ (hepatic , renal, cardical) insufficiency within 5 days prior to allocation. * Any rapidly-progressing disease or immediately life-threatening illness.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Numbers of immune cells in peripheral blood | 6 months after HSCT | PBMCs from HSCT recipients were collected at 1 month, 2 month, 3 month, and 6 month after HSCT, and tested for NK cells, T cells, CMV-specific T cells and their subsets. |
| Incidence of clinically significant CMV infection (CSI) | 6 months after HSCT | Clinically significant CMV infection (CSI) is defined as the administration of antiviral therapy as preemptive therapy for CMV DNAemia or treatment for CMV disease. |
| Incidence of refractory CMV infection and CMV disease | 6 months after HSCT | Refractory CMV infection is defined as a persistent viral load (CMV viral load at the same level or higher than the peak viral load within 1 week but \<1 log10 increase in CMV DNA titers done in the same laboratory and with the same assay) after at least 2 weeks of appropriately dosed antiviral therapy. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Treatment-ralated mortality | Through study completion, an average of 1 year | Treatment-ralated mortality |
| Overall survival | Through study completion, an average of 1 year | Overall survival |
| Incidence of other viral infection and viral-associated disease | 6 months after HSCT | Other viral infection and viral-associated diseases including EBV, ADV, HHV-6, BKV and HSV |
Countries
China
Outcome results
None listed