Antoni notes the opportunity to consider outcomes beyond survival and disease recurrence, the importance of determining optimal timing of interventions, acknowledgment of cancers as different diseases, and the need to identify individuals at high risk for poor outcomes. He discusses application of microarray and bioinformatic analyses (Cole, 2010 and Cole et al., 2005) to demonstrate that an intervention can causally influence inflammatory and metastasis-regulated gene expression in circulating leukocytes from early-stage breast cancer patients (Antoni et al., 2012). Three empirical papers

in this volume focus on cognitive dysfunction due to cancer treatment exposure in breast cancer samples (Ganz et al., 2012, Kesler et al., 2012 and McDonald phosphatase inhibitor library et al., 2012). Ganz et al. conducted an interim cross-sectional analysis of a prospective, longitudinal, observational cohort study to explore associations between proinflammatory cytokines, cerebral functioning, and chemotherapy exposure (Ganz et al., 2012). Similarly, Kesler and colleagues investigated the correlations between hippocampal volume and peripheral cytokine levels in a sample of breast cancer survivors nearly five years post-chemotherapy exposure (Kesler RG7204 cost et al., 2012). The Kesler

et al. and Ganz et al. papers report associations between tumor necrosis factor-alpha (TNF-α) and memory impairments. McDonald and colleagues replicate and extend prior work by their group and others (Kesler et al., 2011 and McDonald et al., 2010). Their current study reports Carnitine dehydrogenase chemotherapy-associated structural brain changes in frontal regions that correspond to concurrent perceptions

of compromised executive function (McDonald et al., 2012). We recognize that these studies have limitations such as small samples sizes, discordance between objective cognitive performance and subjective complaints, and, in some cases, lack of pre/post-treatment and/or non-cancer control comparisons. These limitations beg for prospective longitudinal designs that facilitate pooling of data from different research groups, harmonization of measures, and the use of advanced statistical methods and modeling (Nelson and Suls, in press). Nevertheless, research presented by Ganz et al., Kesler et al., and McDonald et al. nicely illustrates the nexus of brain, behavior, and inflammation. This supplement synthesizes contemporary understanding of PNI in a cancer context and suggests opportunities for further discovery of mechanisms and development of interventions to improve clinical cancer care. Multiple signaling pathways by which the “macroenvironment” can influence the tumor microenvironment are identified, but many unanswered questions remain.