We are very thankful to Crassini et al. for evaluating the impact of infections on overall survival (OS) in their long-term follow-up cohort as a commentary to our paper on predicting infection in CLL.1 They report a significant association between infection during the first year of observation and OS. In the last couple of years, our groups and others have examined the immune dysfunction, both in general but particularly hypogammaglobulinemia, in patients with CLL. Both groups have demonstrated poor survival among CLL patients with hypogammaglobulinemia. Now, Crassini et al. demonstrate that identifying immune dysfunction in terms of early infection is predictive of poor OS.
Within our nationwide cohort of patients diagnosed with CLL in Denmark since 2008, we re-analyzed OS and treatment free survival (TFS) based on whether patients have had an infection during the first year after diagnosis or not.2 All patients alive and treatment-naïve one year after CLL diagnosis were included for this analysis. As demonstrated below, the association (P<0.001) between infection, OS and TFS, as reported by Crassini et al., could be validated in this nationwide cohort (Figure 1 A and B).
When discussing immune dysfunction in CLL in the era of targeted therapies, three important questions warrant further assessment:
References
- Andersen MA, Eriksen CT, Brieghel C. Incidence and predictors of infection among patients prior to treatment of chronic lymphocytic leukemia: a Danish nationwide cohort study. Haematologica. 2018. Google Scholar
- da Cunha-Bang C, Geisler CH, Enggaard L. The Danish National Chronic Lymphocytic Leukemia Registry. Clin Epidemiol. 2016; 8:561-565. Google Scholar
- Sun C, Tian X, Lee YS. Partial reconstitution of humoral immunity and fewer infections in patients with chronic lymphocytic leukemia treated with ibrutinib. Blood. 2015; 19(19):2213-2219. Google Scholar
- Burger JA. Nurture versus Nature: The microenvironment in chronic lymphocytic leukemia. Hematology Am Soc Hematol Educ Program. 2011; 2011:96-103. PubMedhttps://doi.org/10.1182/asheducation-2011.1.96Google Scholar
- Woyach JA, Bojnik E, Ruppert AS. Bruton’s tyrosine kinase (BTK) function is important to the development and expansion of chronic lymphocytic leukemia (CLL). Blood. 2014; 123(8):1207-1213. PubMedhttps://doi.org/10.1182/blood-2013-07-515361Google Scholar
- Niemann CU, Herman SEM, Maric I. Disruption of in vivo chronic lymphocytic leukemia tumor–microenvironment interactions by ibrutinib – findings from an investigator-initiated phase II study. Clin Cancer Res. 2016; 22(7):1572-1582. PubMedhttps://doi.org/10.1158/1078-0432.CCR-15-1965Google Scholar