Biological and Clinical Efficacy of Shingrix in Patients With CLL

Chronic Lymphocytic Leukemia Clinical Trial

Official title:

Biological and Clinical Efficacy of Recombinant Zoster Vaccine (Shingrix) in Patients With Chronic Lymphocytic Leukemia

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06364033
• Other study ID #: CLL2624
• Status: Not yet recruiting
• Phase: N/A
• Start date: August 2024
• Est. completion date: October 2028

Study information

• Verified date: May 2024
• Source: Gruppo Italiano Malattie EMatologiche dell'Adulto
• Contact: Paola Fazi
• Phone: 0670390528
• Email: p.fazi[@]gimema.it
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a biological study. Patients who are eligible to receive Shingrix through the Italian National Health System will be invited to participate in the study. According to AIFA indication, the two doses of vaccine will be administered 4-8 weeks apart. Blood samples will be collected prior to the first vaccine dose (i.e. within the time frame of 3 months prior to the first dose) and 1, 6, 12, 24 and 36 months after the second vaccine dose to evaluate the serological response of Shingrix.

Description:

This is a multi-centre, prospective study, performed on biological samples only. Patients who are eligible to receive Shingrix through the Italian National Health System will be invited to participate in the study.

According to AIFA indication, the two doses of vaccine will be administered 4-8 weeks apart.

Blood samples will be collected prior to the first vaccine dose (i.e. within the time frame of 3 months prior to the first dose) and 1, 6, 12, 24 and 36 months after the second vaccine dose to evaluate the serological response of Shingrix. All protocol procedures (including clinical assessment and blood draws) will be performed during regular follow-up visits according to clinical practice. No additional invasive/dangerous/painful procedures will be required by the study.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 312
• Est. completion date: October 2028
• Est. primary completion date: November 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Diagnosis of CLL or small lymphocytic lymphoma (SLL) or CLL-like MBL according to IWCLL guidelines. Patients must belong to one of the following subgroups:

• Group A: Patients with MBL or previously untreated early-phase CLL/SLL (Binet stage A or RAI stage 0), with no clear signs of disease progression;

• Group B: Patients with active or symptomatic disease according to IWCLL guidelines or with advanced Binet or Rai stages receiving both the first and second vaccine doses before treatment initiation;

• Group C: Patients with CLL/SLL receiving targeted drugs (i.e. ibrutinib/acalabrutinib-based treatment or venetoclax-based treatment) for at least 6 months prior to the administration of the first vaccine dose.

• Age 18 years or older

• Eligible to receive Shingrix according to clinical indication and free of charge through the Italian National Health System

• Life expectancy >6 months

• No active, symptomatic herpes zoster infection or varicella-zoster virus reactivation within 12 months prior to vaccination

• No prior exposure to Shingrix

• Able and willing to provide written informed consent and to comply with the study protocol procedures

Exclusion Criteria:

• Female patients who are currently in pregnancy or are willing to be pregnant

• Any uncontrolled active systemic infection

• Intravenous immunoglobulin (IVIG) administration within 3 months prior to vaccination

• Concomitant use of radiotherapy or chemotherapy

• Hereditary or acquired immunodeficiency syndrome unrelated to CLL

• Chronic use of immunosuppressive medications given for indications that are not CLL-related

Related Conditions & MeSH terms

• Chronic Lymphocytic Leukemia
• Herpes Zoster
• Leukemia
• Leukemia, Lymphocytic, Chronic, B-Cell
• Leukemia, Lymphoid
• Small Lymphocytic Lymphoma

Intervention

Biological:
• serologic response evaluation
Blood samples collection

Locations

Country	Name	City	State
Italy	UOC Ematologia ASST dei Sette Laghi	Varese

Sponsors (1)

Lead Sponsor	Collaborator
Gruppo Italiano Malattie EMatologiche dell'Adulto

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Serologic response evaluation	Rate of positive serologic response to Shingrix in different subsets of patients as determined by antibody response to varicella-zoster virus (=4-fold increase in anti-gE titer from baseline)	at 1 month