Hematologic Malignancy

Humoral and Cellular Immunogenicity of SHINGRIX in Hematologic Malignancy Patients

A measure of the immune response that confers protection against herpes zoster is unknown.

Hematologic Malignancies Humoral Immunogenicity Anti-gE Antibody GMCs infographic
Hematologic Malignancies Cellular Immunogenicity Median frequency for gE-specific CD4+ T-cells infographic
Hematologic Malignancies Humoral Immunogenicity Anti-gE Antibody GMCs infographic
Hematologic Malignancies Cellular Immunogenicity Median frequency for gE-specific CD4+ T-cells infographic

Data are from a descriptive analysis.


*Error bars indicate 95% Cl.

 

Error bars represent 1st and 3rd IQR.

 

ATP=according to protocol; gE=glycoprotein E; GMC=geometric mean concentration;

IQR=interquartile range; M=month; mlU=milli-international units; mL=milliliter.

Study Design

 Study

HEMATOLOGIC MALIGNANCIES [ZOSTER-039]

Phase and trial type/

Total vaccinated cohort

Phase 3

Randomized, observer-blind, placebo-controlled, multinational study.

N=562 [TVC*]1

Patient Population

Adults with hematologic malignancies, ≥18 YOA, SHINGRIX (n=283), Placebo (n=279)1

  • Mean age 57.3 years
  • SHINGRIX: 18 to 49 YOA n=74 (26.1%), ≥50 YOA n=209 (73.9%)
  • Placebo: 18 to 49 YOA n=73 (26.2%), ≥50 YOA n=206 (73.8%)
Dosing Schedule  2-dose series (0.5 mL each) administered 1 to 2 months apart, with the first dose given during or within 6 months of completing immunosuppressive therapy1,†
Study Objectives 

Evaluation of immunogenicity, safety, and reactogenicity1

Patients were excluded if they were vaccinated against herpes zoster or varicella zoster virus within the 12 months preceding the first dose of study vaccine/placebo or had a clinical history of varicella or herpes zoster within the 12 months preceding the first dose of study vaccine/placebo.1

 

*Total vaccinated cohort included all participants who received at least 1 dose of SHINGRIX or placebo.1

For subjects who were vaccinated during a cancer therapy course, each dose was administered with at least 10 days between vaccination and cancer therapy cycles. For subjects who received the vaccination after a full cancer therapy course, the first dose was administered from 10 days to 6 months after cancer therapy had ended.1

 

mL=milliliter; N=total number of patients included in the total vaccinated cohort; n=number of subjects in each group, SHINGRIX or placebo; TVC=total vaccinated cohort; YOA=years of age.

 

The above is not the full list of inclusion or exclusion criteria.

You may also be interested in:

Learn about the safety profile of SHINGRIX in immunocompromised patients aged 18 years and older.

See what CDC says about SHINGRIX.

Learn how to store and properly dose SHINGRIX.