Seroconversion and outcomes after initial and booster COVID‐19 vaccination in adults with hematologic malignancies
MD Thomas A Ollila, MD Rebecca H Masel, MD John L Reagan, MD, PhD Shaolei Lu, Ralph D Rogers, BS, MT, ASCP Kimberly J Paiva, MPH, PA-C Rashida Taher, Ella Burguera‐couce, Adam S Zayac, NP Inna Yakirevich, MD Rabin Niroula, MD Peter Barth, MD Adam J Olszewski
Cancer, doi:10.1002/cncr.34354
BACKGROUND: Patients with hematologic malignancies have impaired humoral immunity secondary to their malignancy and its treatment, placing them at risk of severe coronavirus disease-19 (COVID-19) infection and reduced response to vaccination. METHODS: The authors retrospectively analyzed serologic responses to initial and booster COVID-19 vaccination in 378 patients with hematologic malignancy and subsequently tracked COVID-19-related outcomes. RESULTS: Seroconversion occurred in 181 patients (48%) after initial vaccination; patients who had active malignancy or those who were recently treated with a B-cell-depleting monoclonal antibody had the lowest rates of seroconversion. For initial nonresponders to vaccination, seroconversion after a booster dose occurred in 48 of 85 patients (56%). The seroconversion rate after the booster was similar for patients on (53%) and off (58%) active therapy (p = .82). Thirty-three patients (8.8%) developed a COVID-19 infection, and there were three COVID-19-related deaths (0.8%). Although no significant association was observed between postvaccination seroconversion and the incidence of COVID-19 infection, no patient with seroconversion died from COVID-19, and no patient who received tixagevimab/cilgavimab (N = 25) was diagnosed with a COVID-19 infection. CONCLUSIONS: Booster vaccinations can promote seroconversion in a significant proportion of patients who are seronegative after the initial vaccination course regardless of the specific vaccine or on/off treatment status at the time of revaccination. Although postvaccination seroconversion may not be associated with a decrease in any (including asymptomatic) COVID-19 infection, the authors' experience suggested that effective vaccination (including a booster), supplemented by passive immunization using tixagevimab/cilgavimab in case of lack of seroconversion, effectively eliminated the risk of COVID-19 death in the otherwise high-risk population.
CONFLICT OF INTEREST Thomas A. Ollila reports a grant from the Rhode Island Foundation outside the submitted work. Peter Barth reports personal fees from Celgene and advisory board service at AbbVie, Janssen, and Sanofi-Aventis outside the submitted work. Adam J. Olszewski reports research funding from Genentech, TG Therapeutics, Celldex Pharmaceuticals, and Precision Bio; and grants from Acrotech Pharma, Adaptive Biotechnologies outside the submitted work. The remaining authors made no disclosures.
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'abstract': '<jats:sec><jats:title>Background</jats:title><jats:p>Patients with hematologic malignancies '
'have impaired humoral immunity secondary to their malignancy and its treatment, placing them '
'at risk of severe coronavirus disease‐19 (COVID‐19) infection and reduced response to '
'vaccination.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>The authors '
'retrospectively analyzed serologic responses to initial and booster COVID‐19 vaccination in '
'378 patients with hematologic malignancy and subsequently tracked COVID‐19–related '
'outcomes.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Seroconversion '
'occurred in 181 patients (48%) after initial vaccination; patients who had active malignancy '
'or those who were recently treated with a B‐cell–depleting monoclonal antibody had the lowest '
'rates of seroconversion. For initial nonresponders to vaccination, seroconversion after a '
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'tixagevimab/cilgavimab (<jats:italic>N</jats:italic>\xa0=\xa025) was diagnosed with a '
'COVID‐19 '
'infection.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>Booster '
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'<jats:list-item><jats:p>Patients with hematologic malignancy, especially lymphoma, have an '
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'<jats:list-item><jats:p>In this single‐institution review, less than one half of the patients '
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'<jats:list-item><jats:p>For those who did not make detectable antibodies after initial '
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'\n'
'<jats:list-item><jats:p>By the end of February 2022, 33 of the original 378 patients had a '
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'\n'
'<jats:list-item><jats:p>The only deaths from COVID‐19 were in those who had undetectable '
'antibodies, and no patient who received prophylactic antibody therapy developed a COVID‐19 '
'infection.</jats:p></jats:list-item>\n'
'</jats:list>\n'
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