Blood cancer patients respond to booster dose of Covid-19 vaccination rather than first dose: Study

According to a recent study, less than half of patients with hematologic malignancies developed detectable antibodies after the initial Coid-19 vaccination, but 56 per cent of "nonresponders" developed antibodies after receiving a booster dose.

According to a recent study, less than half of patients with hematologic malignancies developed detectable antibodies after the initial COVID-19 vaccination, but 56 per cent of "nonresponders" developed antibodies after receiving a booster dose. (Also read: Explained: India's Covid 'r' value is over 1.0. What is it?)

The findings of the research were published in the journal 'Cancer'.

For the study, Thomas Ollila, MD, of Brown University, and his colleagues retrospectively analyzed antibody responses to initial and booster COVID-19 vaccination in 378 patients with hematologic malignancies.

Anti-SARS-CoV-2 antibodies were detected in the blood of 181 patients (48 per cent) after initial vaccination with one of three U.S. Food and Drug Administration (FDA)-authorized or approved COVID-19 vaccines, and patients with active cancer or those recently treated with an immune cell-depleting therapy were least likely to produce these antibodies.

Among patients who did not mount an antibody response following initial vaccination, responses were observed after a booster dose in 48 of 85 (56 per cent) patients who were assessed.

By the end of February 2022, 33 patients (8.8 per cent) developed a COVID-19 infection, with three COVID-19-related deaths (0.8 per cent). Although there was no significant link between post-vaccination antibody response and incidence of COVID-19 infection, no patient with antibody responses died from COVID-19.

Also, no patient who received tixagevimab plus cilgavimab was diagnosed with a COVID-19 infection. Tixagevimab and cilgavimab are antibody therapies that bind to non-overlapping portions of the SARS-CoV-2 spike protein, preventing the virus from binding to and infecting cells. The FDA authorized the combination therapy for emergency use during the COVID-19 pandemic as a way to help prevent COVID-19 infection in certain individuals.

"Our findings build on the wealth of literature showing that patients with hematologic malignancies have an impaired response to COVID vaccination. Importantly, we show that many of these patients who did not respond initially will in fact have a response to booster vaccination," said Dr. Ollila.

"Moreover, when we looked at outcomes, we found that deaths from COVID-19 in the patient population we reviewed only occurred in those with undetectable antibodies, and nobody who received prophylactic antibody therapy was diagnosed with COVID-19. This suggests to us the importance of checking antibody levels in these patients and arranging prophylactic antibody therapy."

Dr. Ollila encourages providing booster vaccines for patients and prioritizing prophylactic antibody therapy when indicated. "This is real-world evidence that these actions can save lives," he said.