Eosinophilia in routine blood samples as a biomarker for solid tumor development: A study based on The Copenhagen Primary Care Differential Count (CopDiff) Database

TY - JOUR

T1 - Eosinophilia in routine blood samples as a biomarker for solid tumor development

T2 - A study based on The Copenhagen Primary Care Differential Count (CopDiff) Database

AU - Andersen, Christen Bertel L

AU - Siersma, V.D.

AU - Hasselbalch, H.C.

AU - Lindegaard, H.

AU - Vestergaard, Hanne

AU - Felding, P.

AU - Olivarius, N.de F.

AU - Bjerrum, O.W.

PY - 2014/9/1

Y1 - 2014/9/1

N2 - Background. Eosinophilia may represent an early paraclinical sign of malignant disease and a host anti-tumor effect. The association between eosinophilia and the development of solid tumors has never before been examined in an epidemiological setting. The aim of the present study was to investigate eosinophilia in routine blood samples as a potential biomarker of solid tumor development in a prospective design.Material and methods. From the Copenhagen Primary Care Differential Count (CopDiff) Database, we identified 356 196 individuals with at least one differential cell count (DIFF) encompassing the eosinophil count during 2000-2007. From these, one DIFF was randomly chosen and categorized according to no (< 0.5 × 109/l), mild (≥ 0.5-1.0 × 109/l) or severe (≥ 1.0 × 109/l) eosinophilia. From the Danish Civil Registration System and the Danish Cancer Registry we ascertained all-cause death and solid tumors within the first three years following the DIFF. Using multivariable logistic regression, odds ratios (OR) were calculated and adjusted for previous eosinophilia, sex, age, year, month, C-reactive protein, previous cancer and Charlson's Comorbidity Index.Results. The risk of bladder cancer was increased with mild eosinophilia [OR 1.93 (CI 1.29-2.89), p = 0.0013]. No associations with eosinophilia were observed for the remaining solid cancers.Conclusion. We demonstrate that eosinophilia in routine blood samples associates with an increased risk of bladder cancer. Our data emphasize that additional preclinical studies are needed in order to shed further light on the role of eosinophils in carcinogenesis, where it is still unknown whether the cells contribute to tumor immune surveillance or neoplastic evolution.

AB - Background. Eosinophilia may represent an early paraclinical sign of malignant disease and a host anti-tumor effect. The association between eosinophilia and the development of solid tumors has never before been examined in an epidemiological setting. The aim of the present study was to investigate eosinophilia in routine blood samples as a potential biomarker of solid tumor development in a prospective design.Material and methods. From the Copenhagen Primary Care Differential Count (CopDiff) Database, we identified 356 196 individuals with at least one differential cell count (DIFF) encompassing the eosinophil count during 2000-2007. From these, one DIFF was randomly chosen and categorized according to no (< 0.5 × 109/l), mild (≥ 0.5-1.0 × 109/l) or severe (≥ 1.0 × 109/l) eosinophilia. From the Danish Civil Registration System and the Danish Cancer Registry we ascertained all-cause death and solid tumors within the first three years following the DIFF. Using multivariable logistic regression, odds ratios (OR) were calculated and adjusted for previous eosinophilia, sex, age, year, month, C-reactive protein, previous cancer and Charlson's Comorbidity Index.Results. The risk of bladder cancer was increased with mild eosinophilia [OR 1.93 (CI 1.29-2.89), p = 0.0013]. No associations with eosinophilia were observed for the remaining solid cancers.Conclusion. We demonstrate that eosinophilia in routine blood samples associates with an increased risk of bladder cancer. Our data emphasize that additional preclinical studies are needed in order to shed further light on the role of eosinophils in carcinogenesis, where it is still unknown whether the cells contribute to tumor immune surveillance or neoplastic evolution.

KW - blood

KW - care

KW - Eosinophilia

KW - PRIMARY-CARE

KW - semrap-2014-1

U2 - 10.3109/0284186X.2014.887857

DO - 10.3109/0284186X.2014.887857

M3 - Journal article

C2 - 24913152

SN - 1100-1704

VL - 53

SP - 1245

EP - 1250

JO - Acta Oncologica, Supplement

JF - Acta Oncologica, Supplement

IS - 9

ER -