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ePoster Display

1602P - COVID-19 vaccination efficacy in cancer patients: An ongoing prospective trial

Date

16 Sep 2021

Session

ePoster Display

Topics

Cancer Treatment in Patients with Comorbidities;  Clinical Research;  COVID-19 and Cancer

Tumour Site

Presenters

Tiago Filipe Da Cruz Tomas

Citation

Annals of Oncology (2021) 32 (suppl_5): S1129-S1163. 10.1016/annonc/annonc713

Authors

T.F. Da Cruz Tomas1, I.F. Eiriz1, M. Vitorino1, R.S. Vicente1, A.D. Mendes1, M.C. Silva Sousa1, S. Braga1, T.M. Fiuza1, L.A. Gonçalves2, C.P. Gonçalves3, J. Demengeot4

Author affiliations

  • 1 Medical Oncology Department, Hospital Professor Doutor Fernando Fonseca, 2720-276 - Amadora/PT
  • 2 Viral Infection Unit, Instituto Gulbenkian de Ciência, 2780-156 - Oeiras/PT
  • 3 Disease Genetics Unit, Instituto Gulbenkian de Ciência, 2780-156 - Oeiras/PT
  • 4 Lymphocytes Physiology Unit, Instituto Gulbenkian de Ciência, 2780-156 - Oeiras/PT

Resources

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Abstract 1602P

Background

Cancer patients (pts) have higher risk of severe COVID-19 infection. However, observations are based on non-comparative retrospective studies. Evidence regarding vaccination in cancer pts is limited, but there is enough evidence to support COVID-19 vaccination, even under active treatment. Data on humoral and cellular immune response to antiviral vaccination in cancer pts are scarce. In pts receiving immunosuppressive therapies (IST) like chemotherapy and targeted therapies, seroconversion/protection rates are expected to be lower than general population, but not in pts receiving immune checkpoint inhibitors (ICI). Serum antibodies against an infectious agent may be an immunity indicator.

Methods

Prospective observational longitudinal study with the intent of evaluating the humoral response of cancer pts to COVID-19 vaccination. The study includes pts diagnosed in any stage, without or under active treatment, or survivors followed in Hospital Prof. Dr. Fernando Fonseca, in partnership with Instituto Gulbenkian de Ciência. Pts are divided into 4 arms, independently of the vaccine: A – IST; B – ICI; C –Hormone therapy (HT); D – Cancer survivors. Recruitment started in March 2021, expecting at least 50 pts per arm. IgG, IgA and IgM anti-SARS-CoV-2 antibodies ELISA determination in 9 timepoints: before 1st dose and at the 3rd, 6th, 12th, 15th, 24th, 36th, 48th and 60th weeks post 1st dose. Side effects’ questionnaire will be implemented after 1st and 2nd doses.

Results

Recruitment is ongoing and a total of 202 pts were enrolled, of which 178 pts have 3-weeks post 1st dose evaluated: 101 in arm A: 11 in B: 31 in C; and 35 in D.The mean age is 61.6 years, with 53.4% females. Regarding vaccines, 55 pts were submitted to ChAdOx1-S/nCoC-19, 5 to Ad26.COV2.S, 89 to BNT162b2 and 12 to mRNA-1273 vaccines. At 3 weeks, 33/97 pts (34%) in arm A, 2/11 pts (18%) in B, 14/28 pts (50%) in C and 15/35 pts (43%) in D already generated anti-spike IgG. Most common side effects were local inflammatory reaction (47%), generalized muscle pain (17%), fatigue (11%), and chills (10%).

Conclusions

Efficacy and safety profiles of vaccines against COVID-19 infection in cancer pts is still unknown.This study hopes to assess differences in immunization between pts’ treatment profiles and duration profiles and safety profiles.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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