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NCT Number: NCT06058858

Incidence and Risks Factors of CMV Reactivation in Patients Receiving of CAR-T Cells for Acute Leukemia and Lymphoma Relapse, a Cohort Study Analysis

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.

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Key information

Age range

1 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Hopital Robert Debré - APHP, Paris, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Common inclusion criteria :

  • Paediatric (1 to 18 years old) receiving CART-T cells treatment for refractory acute leukemia or B-cell lymphoma
  • Adult receiving CART-T cells treatment for refractory acute leukemia or B-cell lymphoma
  • CMV seropositive patients

Inclusion criteria

retrospective part

  • Provide written non-opposition from the patient signed by investigator
  • If the patient is a minor, provide written non-opposition from both parents and child (if age appropriate to collect their non-objection) or child and the legal representative in case only one parent is alive, signed by investigator

Inclusion criteria

prospective part

  • Provide written consent form signed by patient and investigator
  • If the patient is a minor, provide written consent form signed by investigator and both parents or signed by investigator and the legal representative in case only one parent is alive

Exclusion criteria

  • CMV seronegative patients
  • Lack of affiliation to a social security scheme (as a beneficiary or assignee)
  • Patients under guardianship / curatorship
  • Patient under AME (state medical aid)

Treatment and study plan

Primary outcomes

  1. Rate of CMV reactivation

    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).

Secondary outcomes

  1. Rate of CMV disease

    Time frame: Up to 3 months

  2. Rate of anellovirus infection

    Time frame: Up to 3 months

  3. Rate of pegivirus infection

    Time frame: Up to 3 months

  4. Rate of redondovirus infection

    Time frame: Up to 3 months

  5. Correlation between CMV reactivation and the occurrence of other bacterial or fungal infections

    Time frame: Up to 3 months

  6. Correlation between CMV reactivation and the expansion of CAR-T cells

    Time frame: Up to 3 months

  7. Correlation between CMV reactivation and other early viral persistent reactivations (anellovirus, pegivirus, redondovirus)

    Time frame: Up to 3 months

  8. Rate of CMV reactivation in patients with acute leukemia

    Time frame: Up to 3 months

  9. Rate of CMV reactivation in patients with lymphoma

    Time frame: Up to 3 months

  10. Detection of mutations in the CMV DNA polymerase gene in patients under acyclovir or valacyclovir prophylaxis

    Time frame: Up to 3 months

  11. Health related quality of life (HRQL)) of the study population with or without CMV activation

    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.

  12. Cost of illness of CMV disease

    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)

Study contacts

Contact information is provided by the study sponsor or research team.

Jérôme Lambert, Pr

CONTACT

[email protected]

+33142499742

Jérôme Le Goff, Pr

CONTACT

[email protected]

+33142499493

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Acronym: CMV CAR-T

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Sep 28, 2023
Registry last updated
Jul 17, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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