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. 2022 Sep 27;3(10):100781. doi: 10.1016/j.xcrm.2022.100781

Table 3.

Association of clinical parameters with detectable NAb against Omicron

Patients (n) Detectable NAb against Omicron BA.1
Detectable NAb against Omicron BA.2
OR (95% CI) p OR (95% CI) p
Blood cancer patients 80
Intercept 2.80 (0.68–15.17) 0.26 3.54 (0.78–23.45) 0.21

Diagnosis (vs. acute leukemia)

Chronic lymphocytic leukemia 16/80 3.48 (0.46–2.45) 0.30 7.41 (0.78–109.31) 0.16
Myelodysplastic syndrome 3/80 1.21 (0.06–28.03) 0.91 N/A 0.99
Myeloma 33/80 9.53 (0.88–131.13) 0.13 N/A 0.99
Lymphoma 21/80 8.07 (0.88–97.32) 0.13 2.49 (1.90–606.61) 0.06

Vaccine type (first and second dose)

BNT162b2 (vs. ChAdOx1) 35/80 0.46 (0.13–1.61) 0.31 0.28 (0.04–1.47) 0.23
Previous COVID-19
SARS-CoV-2 infection before second vaccine dose 11/80 6.52 (1.13–51.90) 0.10 4.08 (0.52–57.99) 0.30

Anti-cancer therapya

B cell-depleting therapy (anti-CD20 [within 12 months] or BTKi [within 28 days]) 15/80 0.03 (0.003–0.14) 0.0013 0.06 (0.004–0.41) 0.04
Chemo- or targeted therapy 34/80 0.68 (0.10–4.17) 0.74 0.55 (0.03–11.24) 0.72

NAbs were binned in detected (≥40) or undetected (<40). All values were caclulated using multivariable binary logistic regression. BTKi, Bruton’s tyrosine kinase inhibitor; OR, odds ratio; CI, confidence interval; p, p-value.

a

For anti-cancer therapy, the indicated treatment was tested for patients who received the treatment vs. patients not receiving that treatment.