R-MVST Cells for Treatment of Viral Infections in Children and Young Adults
NCT06926894
Adenoviridae Infections, Adenovirus
New York, United States
View Trial DetailsNCT Number: NCT06058858
Letermovir is approved for the primary prevention of Cytomegalovirus (CMV) reactivation and infection in hematopoietic stem cell transplant recipients. Letermovir may be beneficial in other clinical presentation where CMV reactivates and may alter clinical outcomes. Recently Chimeric Antigen Receptor (CAR) T cells have been used for the treatment of refractory acute leukemia and B cell lymphoma. Reactivation of chronic viral infections, in particular those belonging to the Herpesviridae family can therefore be observed following CAR-T cells treatment.According to first reports, Cytomegalovirus seems to be the main virus detected. Uncontrolled CMV reactivation leads to CMV disease requiring the use of antiviral drugs associated with either hematological toxicity (ganciclovir) or renal toxicity (foscarnet) and is usually associated with poor outcomes. In addition, CMV interplays with the immune system and decreases the immunosurveillance of tumor cells and facilitates the growth or reactivation of other opportunistic infections. Therefore, CMV reactivation could also impact the outcome of CART cells treatment by increasing the existing risk of opportunistic infections in CART cells recipients and thus by increasing morbidity, length stay or require intensive care. Imbalance of the immune system usually correlates with reactivation of persistent virus like Torquetenovirus (TTV), redondovirus or pegivirus found more frequently in Hematopoietic stem-cell transplantation (HSCT) patients or patients requiring intensive care. Whether reactivations of those persistent viruses are associated or precede CMV reactivation deserve careful investigation to identify as early as possible patients at high risk and who could benefit from antiviral preventive treatment.
The objective of this trial is to determine the incidence of CMV reactivation within 3 months after infusion of CAR-T cells in CMV seropositive patients with refractory acute leukemia or B-cell lymphoma.
Interested in participating?
Request Info1 year–100 year
All sexes
Observational
Hopital Robert Debré - APHP, Paris, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Common inclusion criteria :
Inclusion criteria
retrospective part
Inclusion criteria
prospective part
Exclusion criteria
Time frame: Up to 3 months after inclusion
Rate of CMV reactivation occurring within the first 3 months after CAR-T-cell infusion in paediatric and adult patients treated for refractory B cell acute lymphoblastic leukemia (B-ALL) and diffuse large B-cell lymphoma (DLBCL).
Time frame: Up to 3 months
Time frame: Up to 3 months
Time frame: Up to 3 months
Time frame: Up to 3 months
Time frame: Up to 3 months
Time frame: Up to 3 months
Time frame: Up to 3 months
Time frame: Up to 3 months
Time frame: Up to 3 months
Time frame: Up to 3 months
Time frame: Up to 3 months
EQ-5D-5L scale (adult) EQ-5D-Y scale (child) First part describes 5 dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression) Second part is a visual analogue scale with a score varying from 0 to 100; the higher the score the better the state of health.
Time frame: Up to 3 months
Illness of CMV disease is defined by prolonged initial hospitalization, additional hospitalizations, increased surveillance in case of reactivation (consults and biological sampling), treatments)
Contact information is provided by the study sponsor or research team.
Jérôme Lambert, Pr
CONTACT
Jérôme Le Goff, Pr
CONTACT
Assistance Publique - Hôpitaux de Paris
Other
Acronym: CMV CAR-T
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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