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. 2023 Apr 27;18(4):e0275356. doi: 10.1371/journal.pone.0275356

Table 1. Characteristics of recipients of tixagevimab-cilgavimab (T/C) who developed COVID-19 infection between December 19, 2021 and July 31, 2022 when Omicron was the dominant circulating variant.

Characteristics of T/C recipients who were infected prior to receiving T/C (pre-T/C) are compared with characteristics of T/C recipients who were diagnosed with COVID after having received any dose of T/C (post-T/C).

Patient Characteristic Patients with COVID-19 infection pre-T/C (n = 105) Patients with COVID-19 infection post-T/C (n = 102) p-value
Median age [range], years 54.0 [18–79] 60.5 [25–99] p = 0.008
Patient gender N.S.
Male (%) 58 (55.2) 58 (56.9)
Female (%) 47 (44.8) 44 (43.1)
Underlying conditions N.S.
Solid organ transplantation (%) 43 (41.0) 35 (34.3)
Hematologic malignancy or bone marrow transplantation (%) 46 (43.8) 56 (54.9)
Other (%) 16 (15.2) 11 (10.8)
Number (%) of vaccine doses received prior to COVID diagnosis p < 0.001
0 15 (14.3) 3 (2.9)
1–2 29 (27.6) 25 (24.8)
3 53 (50.5) 36 (35.6)
4 8 (7.6) 37 (36.6)
Therapeutics received (%) * p ≤ 0.001
Nirmatrelvir-Ritonavir 5 (4.8) 40 (39.2)
Bebtelovimab 0 (0.0) 34 (33.3)
Remdesivir 18* (17.1) 17 (16.7)
Sotrovimab 57* (54.3) 2 (2.0)
None 26 (24.8) 9 (8.8)
Number of patients hospitalized (%) 26 (24.8) 6 (5.9) p < 0.001
Number of ICU admissions (%) 7 (6.7) 0 (0.0) p = 0.008
Number of deaths from COVID-19 (%) 0 (0.0) 0 (0.0)

Including autoimmune conditions, HIV/AIDS, and solid tumor malignancy

One patient’s vaccine history was not documented within the electronic medical record

*One patient was treated with both sotrovimab and remdesivir

Abbreviations:

ICU = Intensive Care Unit