Mediating Effects of Diagnostic Route on the Comorbidity Gap in Survival of Patients with Diffuse Large B-Cell or Follicular Lymphoma in England
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MDPI
Materia
Diffuse large B-cell lymphoma Follicular lymphoma Mediation analysis Epidemiology Comorbidity Survival
Date
2022-10-17Referencia bibliográfica
Smith, M.J.; Rachet, B.; Luque-Fernandez, M.A. Mediating Effects of Diagnostic Route on the Comorbidity Gap in Survival of Patients with Diffuse Large B-Cell or Follicular Lymphoma in England. Cancers 2022, 14, 5082. [https://doi.org/10.3390/cancers14205082]
Sponsorship
Cancer Research UK C7923/A18525Abstract
Background: Socioeconomic inequalities in survival from non-Hodgkin lymphoma persist.
Comorbidities are more prevalent amongst those in more deprived areas and are associated with
diagnostic delay (emergency diagnostic route), which is also associated with poorer survival probability.
We aimed to describe the effect of comorbidity on the probability of death mediated by diagnostic
route (emergency vs. elective route) amongst patients with diffuse large B-cell (DLBCL) or follicular
lymphoma (FL). Methods: We linked the English population-based cancer registry and hospital
admission records (2005–2013) of patients aged 45–99 years. We decomposed the effect of comorbidity
on survival into an indirect effect acting through diagnostic route and a direct effect not mediated by
diagnostic route. Furthermore, we estimated the proportion of the comorbidity effect on survival
mediated by diagnostic route. Results: For both DLBCL (n = 27,379) and FL (n = 14,043), those with
any comorbidity, or living in more deprived areas, were more likely to experience diagnostic delay
and poorer survival. The indirect effect of comorbidity on mortality through diagnostic route was
highest at 12 months since diagnosis (DLBCL: Odds Ratio 1.10 [95% CI 1.07–1.13], FL: OR 1.09 [95%
CI 1.04–1.14]). Within the first 12 months since diagnosis, emergency diagnostic route accounted for
24% (95% CI 17.5–29.5) and 16% (95% CI 6.0–25.6) of the comorbidity effect on mortality, for DLBCL
and FL, respectively. Conclusion: Efforts to reduce diagnostic delay (emergency diagnosis) amongst
patients with comorbidity would reduce inequalities in DLBCL and FL survival by 24% and 16%,
respectively. Further public health programs and interventions are needed to reduce diagnostic delay
amongst lymphoma patients with comorbidities.