Cancer
Conditions
Keywords
COVID-19, Vaccine, Pfizer, Moderna, Janssen, COVID
Brief summary
The goals of this study are to assess initial or booster vaccine performance (safety and efficacy) and to collect serum and peripheral blood mononuclear cells (PBMCs) pre and post-vaccination to assess immune and other response parameters following immunization in cancer patients receiving either the Pfizer (BTN162b2), Moderna (mRNA-1273), or the Janssen (Ad26.COV2.S) vaccines.
Interventions
BIOLOGICALCOVID-19 Vaccination
Subjects will receive either the Moderna (mRNA-1273), Pfizer (BTN162b2), or Janssen (Ad26.COV2.S) vaccination per standard of care
Sponsors
Indiana University
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
1. Ability to provide written informed consent and HIPAA authorization 2. Patients deemed eligible and willing to receive a COVID-19 vaccine by treating physician per standard of care. 3. Subjects must be ≥ 18 years old at the time of consent. 4. Diagnosis of cancer and fall into one of the groups below: 1. Group 1: Patients with solid tumors receiving courses of cytotoxic therapy. 2. Group 2: Patients with hematological cancers receiving courses of cytotoxic chemotherapy. 3. Group 3: Patients with solid tumors receiving tyrosine kinase inhibitors (TKIs) or other targeted therapies, but not cytotoxic regimens within 3 months. 4. Group 4: Patients with hematologic cancers receiving TKIs or other targeted therapies, but not cytotoxic regimens within 3 months. 5. Group 5: Patients receiving immune checkpoint inhibitors. 6. Group 6: Patients who underwent allogeneic stem cell transplant within 12 months. 7. Group 7: Patients who underwent cellular therapy, including Chimeric antigen receptor t-cells (CAR-T) cells or t-cells with engineered t-cell receptors (TCRs) within 12 months. 8. Group 8: Patients in remission who have received cellular therapy more than 12 months in the past, including allogeneic, autologous or engineered cellular approaches. 9. Group 9: Patients with cancer in remission for at least 2 years not receiving active cytotoxic cancer chemotherapy (hormonal therapy is permitted). 10. Group 10: Patients who have undergone allogenic bone marrow transplant and are currently receiving immunosuppressants 11. Group 11: Patients who have undergone allogenic bone marrow transplant who are not currently receiving immunosuppressants 12. Group 12: Patients who have a cancer diagnosis but do not fall into group 1-11 3\. Estimated survival of 8 weeks or more following enrollment on the study.
Exclusion criteria
1. Uncontrolled intercurrent illness including, but not limited to, ongoing or active COVID-19 infection or influenza-like-illness. If subjects have previously tested positive for COVID-19 infection, they are eligible to participate in this study after 90 days 2. Unwilling or unable to follow protocol requirements.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adverse Event Collection | from date of vaccination until 2 months after full vaccination |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of COVID-19 infection | from date of vaccination until 6 months after full vaccination |
Countries
United States
Outcome results
None listed