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Safety and Immunogenicity of Prime-boost Vaccination of SARS-CoV-2 in Patients With Cancer

B

Beijing 302 Hospital

Status and phase

Unknown
Phase 2
Phase 1

Conditions

COVID-19
Vaccine Reaction
Patients With Cancer

Treatments

Biological: Coronavirus vaccination

Study type

Interventional

Funder types

Other

Identifiers

NCT05273541
ky-2021-7-9-2

Details and patient eligibility

About

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has caused a global pandemic since late 2019 that resulted in more than 360 million population infection. Patients with cancers may be at higher risk of infection and severity than those without cancer. Mass vaccination has been carried out, but reinfection and vaccine breakthrough cases still occur. Now, the prime-boost regimen was identified safe and efficient, but the reactogenicity and immunogenicity of prime-boost vaccine strategy in cancer patients were not known.

Full description

This study is a prospective, single-arm, open-label clinical trial. A total of 100 patients with different cancers including breast cancer, hepatocellular carcinoma, lung cancer, esophageal cancer, gastric cancer and colorectal cancer were included in this heterologous prime-boost vaccination study. All of the patients will further accept 12 months follow-up study after prime-boost vaccination. Safety, reactogenicity and immunogenicity of the prime-boost vaccination in those patients will be carefully recorded and detected.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age above 18 years.
  2. Patients with diagnosed cancers including breast cancer, hepatocellular carcinoma, lung cancer, esophageal cancer, gastric cancer and colorectal cancer.
  3. Patients who have received local or systemic anti-cancer therapies according to the treatment guidelines previously or currently, and have a stable condition with the ECOG score below 2.
  4. The functions of multi-organs were normal or basically normal, and there are no contraindications for vaccination.

Exclusion criteria

  1. Patients with acute attack of chronic diseases.

  2. Patients have history of convulsion, epilepsy, encephalopathy and psychosis. Patients who are allergic to any component of the vaccine, or have a serious history of vaccine allergy.

  3. Pregnant or lactating women.

  4. Sufferring serious cardiovascular diseases, such as arrhythmia, conduction block, myocardial infarction, and severe hypertension can not be well controlled by drugs.

    Patients have severe chronic diseases or diseases can not be controlled well during the progress, such as asthma, diabetes, thyroid disease, etc. Congenital or acquired angioedema / neuroedema.

  5. Systemic cytotoxic drugs, cell therapies including NK cells, cytokine induced killer cells, Dendritic cells, CTL and stem cells infusion are required during vaccination.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

Prime-boost vaccination
Experimental group
Description:
Patients in the experimental group need to accept the prime-boost vaccination regimen
Treatment:
Biological: Coronavirus vaccination

Trial contacts and locations

1

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Central trial contact

Ruonan Xu, MD; Fu-Sheng Wang, MD

Data sourced from clinicaltrials.gov

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