Immunogenicity and safety of the CoronaVac vaccine in patients with cancer receiving active systemic therapy
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Erişim
info:eu-repo/semantics/closedAccessTarih
2021Yazar
Karaçin, CengizEren, Tülay
Zeynelgil, Esra
İmamoğlu, Göksen İnanç
Altınbaş, Mustafa
Karadağ, İbrahim
Başal, Fatma Buğdaycı
Bilgetekin, İrem
Sütçüoğlu, Osman
Yazıcı, Ozan
Özdemir, Nuriye
Özet, Ahmet
Yıldız, Yeşim
Esen, Selin Aktürk
Uçar, Gökhan
Uncu, Doğan
Dinç, Bedia
Aykan, Musa Barış
Ertürk, İsmail
Karadurmuş, Nuri
Civelek, Burak
Çelik, İsmail
Ergun, Yakup
Doğan, Mutlu
Öksüzoğlu, Ömür Berna
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Tüm öğe kaydını gösterKünye
Karacin, C., Eren, T., Zeynelgil, E., Imamoglu, G. I., Altinbas, M., Karadag, I., Basal, F. B., Bilgetekin, I., Sutcuoglu, O., Yazici, O., Ozdemir, N., Ozet, A., Yildiz, Y., Esen, S. A., Ucar, G., Uncu, D., Dinc, B., Aykan, M. B., Erturk, İ., Karadurmus, N., … Oksuzoglu, O. B. (2021). Immunogenicity and safety of the CoronaVac vaccine in patients with cancer receiving active systemic therapy. Future oncology (London, England), 17(33), 4447–4456. https://doi.org/10.2217/fon-2021-0597Özet
Aim: To evaluate the immunogenicity and safety of the CoronaVac vaccine in patients with cancer receiving active systemic therapy. Methods: This multicenter, prospective, observational study was conducted with 47 patients receiving active systemic therapy for cancer. CoronaVac was administered as two doses (3 mu g/day) on days 0 and 28. Antibody level higher than 1 IU/ml was defined as 'immunogenicity.' Results: The immunogenicity rate was 63.8% (30/47) in the entire patient group, 59.5% (25/42) in those receiving at least one cytotoxic drug and 100% (five of five) in those receiving monoclonal antibody or immunotherapy alone. Age was an independent predictive factor for immunogenicity (odds ratio: 0.830; p = 0.043). Conclusion: More than half of cancer patients receiving active systemic therapy developed immunogenicity.
Tweetable abstract Immunogenicity developed with CoronaVac in 25 (59.5%) of 42 patients who received at least one cytotoxic drug and in all patients (n = 5) who received monoclonal antibody or immunotherapy alone.