Abstract
The t(14;18) chromosomal translocation is the most common cytogenetic abnormality in non‐Hodgkin lymphoma (NHL), occurring in 70–90% of follicular lymphomas (FL) and 30–50% of diffuse large B‐cell lymphomas (DLBCL). Previous t(14;18)‐NHL studies have not evaluated risk factors for NHL defined by both t(14;18) status and histology. In this population‐based case‐control study, t(14;18) status was determined in DLBCL cases using fluorescence in situ hybridization on paraffin‐embedded tumor sections. Polytomous logistic regression was used to evaluate the association between a wide variety of exposures and t(14;18)‐positive (N = 109) and ‐negative DLBCL (N = 125) and FL (N = 318), adjusting for sex, age, race, and study center. Taller height, more lifetime surgeries, and PCB180 exposure were associated with t(14;18)‐positivity. Taller individuals (third tertile vs. first tertile) had elevated risks of t(14;18)‐positive DLBCL (odds ratio [OR] = 1.8, 95% confidence interval [CI] 1.1–3.0) and FL (OR = 1.4, 95%CI 1.0–1.9) but not t(14;18)‐negative DLBCL. Similar patterns were seen for individuals with more lifetime surgeries (13+ vs. 0–12 surgeries; t(14;18)‐positive DLBCL OR = 1.4, 95%CI 0.7–2.7; FL OR = 1.6, 95%CI 1.1–2.5) and individuals exposed to PCB180 greater than 20.8 ng/g (t(14;18)‐positive DLBCL OR = 1.3, 95%CI 0.6–2.9; FL OR = 1.7, 95%CI 1.0–2.8). In contrast, termite treatment and high alpha‐chlordane levels were associated with t(14;18)‐negative DLBCL only, suggesting that these exposures do not act through t(14;18). Our findings suggest that putative associations between NHL and height, surgeries, and PCB180 may be t(14;18)‐mediated and provide support for case‐subtyping based on molecular and histologic subtypes. Future efforts should focus on pooling data to confirm and extend previous research on risk factors for t(14;18)‐NHL subtypes.