Abstract 2285P
Background
Due to a compromised immune system, cancer patients are more prone to have a weaker response to COVID-19 vaccination, which can lead to a worst outcome. Thus it is crucial to evaluate the immunological response of cancer patients to booster doses of the vaccine to stratify the patients accordingly and provide a better care.
Methods
Vaccinated cancer patients from the Portuguese Oncology Institute of Porto, under active cancer treatment with different types of solid tumours (SL) and liquid tumours (LT) were included to study the potential differences in the response to COVID-19 booster dose vaccine according to tumour type. Humoral immune response to the booster dose of the COVID-19 vaccine was evaluated in patients’ serum samples analysing IgG levels against SARS-CoV-2 Spike (S) protein. We also analysed the IgG levels against SARS-CoV-2 Nucleocapsid (N) protein to address previous contact with the virus. The first cohort of patients collected samples before the booster dose and 3 and 6 months after (cohort 1, N=54, SL=44, LT=10) and the other cohort collected samples only 3 and 6 months after booster dose (cohort 2, N=71, SL=45, LT=26). A group of vaccinated healthy individuals (N=83) was also analysed, and they collected samples at 3 and 6 months post-boost.
Results
Regarding cohort 1, for solid tumours, we observed that IgG S levels increased 3 months after boost (p<0.001) and remained high at 6 months post-boost (p<0.001) when compared to pre-boost. One the other hand, the hematologic tumours demonstrated a weak response to vaccination since IgG S levels remained very low 3 and 6 months after the boost. When comparing 3 months post-boost in both cohorts and healthy individuals, we observed that the healthy individuals had the strongest IgG S response, followed by the solid and, lastly, the hematologic tumours. In fact, the difference between solid and haematological tumours was quite significant (p=0.017).
Conclusions
We verified that the type of tumour may influence COVID-19 vaccination efficacy since solid cancer patients had a better response to SARS-CoV-2 vaccination when compared to haematological cancer patients. Moreover, as expected, healthy individuals have a stronger immune response when compared to cancer patients.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Rui Medeiros, Júlio Oliveira.
Funding
AstraZeneca.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
2262P - Baseline-informed versus tumor-agnostic minimal residual disease (MRD) concordance study in patients with HER2+ gastroesophageal adenocarcinoma patients
Presenter: Pan Du
Session: Poster session 08
2263P - Ethnicity-specific distribution of BRCA1, BRCA2, PALB2 and ATM pathogenic alleles in breast and ovarian cancer patients from the North Caucasus
Presenter: Evgeny Imyanitov
Session: Poster session 08
2264P - Proteomics-based phenotypic classification of non-smallcell lung cancer
Presenter: Olena Berkovska
Session: Poster session 08
2265P - miR-4487 enhances gefitinib-mediated ubiquitination and autophagic degradation of EGFR in non-small cell lung cancer cells by targeting USP37
Presenter: Sei-Hoon Yang
Session: Poster session 08
2266P - IMMUcan consortium: Focus on the first results of the non-small cell lung cancer (NSCLC) cohort
Presenter: Marie Morfouace
Session: Poster session 08
2267P - Coronary heart disease and risk of lung cancer: A two-sample Mendelian randomization study
Presenter: Cai Chen Li
Session: Poster session 08
2269P - Patient derived xenografts generated from circulating cancer stem cells on chorioallantoic membrane as an alternative pre-clinical model for personalized medicine in pancreatic cancer
Presenter: Monika Pizon
Session: Poster session 08
2270P - Integrative analyses of bulk and single-cell RNA-seq identified diabetes mellitus-related signature as a prognostic factor in pancreatic adenocarcinoma
Presenter: Le Tang
Session: Poster session 08
2271P - Development of an oncolytic virus for the treatment of high grade serous ovarian cancer and other stromal rich tumours
Presenter: Miriam Bazan Peregrino
Session: Poster session 08
2272P - Minimal DNA-methylation (DNAm) signatures for non-invasive tumor-agnostic estimation of tumor content (TC) and molecular subtype in patients (pts) with metastatic breast cancer (mBC)
Presenter: Matteo Benelli
Session: Poster session 08