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. 2022 Aug 31;14(17):4252. doi: 10.3390/cancers14174252

Table 1.

Baseline characteristics.

Characteristics Patients
N = 68
n (%)
Age, median years (IQR) 66 (59–75)
Male 38 (56)
Race
 Black or African American 1 (2)
 Hispanic or Latino 11 (16)
 White 45 (66)
 Other 11 (16)
Disease type
 Burkitt’s, DLBCL, PMBL 20 (29)
 CLL/SLL 14 (21)
 Hodgkin’s lymphoma (HL) 2 (3)
 Indolent lymphomas 20 (29)
 Mantle cell lymphoma (MCL) 3 (4)
 T-cell lymphomas (TCLs) 6 (10)
 Other § 3 (4)
Comorbidities
 Cardiovascular disease 23 (34)
 COPD 5 (7)
 Autoimmune disease †† 5 (7)
 Mild liver disease ‡‡ 2 (3)
 Diabetes 19 (28)
 Chronic kidney disease 6 (10)
 HIV/AIDS 1 (2)
 Smoking history
 Current smoker 3 (4)
 Former smoker 18 (27)
Absolute neutrophil count at COVID-19 diagnosis
 Median cells × 103 (IQR) 3.25 (2.175–4.7)
 Less than or equal to 1000 cells/mm3 6 (9)
Absolute lymphocyte count at COVID-19 diagnosis
 Median cells × 103 (IQR) 1.1 (0.7–1.625)
 Less than or equal to 500 cells/mm3 15 (22)
Vaccine received
 Pfizer-BioNTech 28 (41)
 Moderna 24 (35)
 Johnson & Johnson 1 (2)

DLBCL—diffuse large B-cell lymphoma; PMBL—primary mediastinal B-cell lymphoma; CLL—chronic lymphocytic leukemia; SLL—small lymphocytic lymphoma; COPD—chronic obstructive pulmonary disease; HIV—human immunodeficiency virus; AIDS—acquired immunodeficiency syndrome. Indolent lymphomas included a diagnosis of one of the following: follicular lymphomas, marginal zone lymphoma, lymphoplasmacytic lymphoma, and Waldenstrom macroglobulinemia; T-cell lymphomas included a diagnosis of one of the following: peripheral T-cell lymphomas not otherwise specified (NOS), anaplastic large cell lymphoma (ALCL), cutaneous T-cell lymphomas, angioimmunoblastic T-cell lymphoma (AITL), and acute T-cell leukemia/lymphoma (ATLL); § included Langerhans histiocytosis, hemophagocytic lymphohistiocytosis (HLH), and T-cell large granular lymphocytic leukemia (T-LGL); cardiovascular disease was defined as history of coronary artery disease, hypertension, or cerebrovascular accident; †† autoimmune disease included a diagnosis of one of the following: autoimmune disease, rheumatological disorders, and connective tissue disease; ‡‡ mild liver disease was defined as a history of chronic hepatitis or cirrhosis without portal hypertension.