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(http://www.niehs.nih.gov//portfolio/index.cfm?do=portfolio.grantdetail&&grant_number=R01ES034079&format=word)
| Principal Investigator: Birmann, Brenda M | |
|---|---|
| Institute Receiving Award | Brigham And Women'S Hospital |
| Location | Boston, MA |
| Grant Number | R01ES034079 |
| Funding Organization | National Institute of Environmental Health Sciences |
| Award Funding Period | 15 Jan 2024 to 31 Oct 2028 |
| DESCRIPTION (provided by applicant): | Project Summary/Abstract Non-Hodgkin lymphoma (NHL) and multiple myeloma (MM) are cancers arising from mature lymphocytes that collectively pose a substantial public health, personal and financial burden. Present knowledge of their etiology is inadequate to inform prevention strategies; data from prospective studies, and for specific histologic subtypes, are particularly limited. Inflammation, heightened immune activation and growth factor dysregulation contribute to their pathogenesis, as indicated, for example, by well-known associations of NHL risk with severe immune compromise and with pre-diagnosis plasma immune marker profiles that indicate inflammation and B- cell activation, as well as by consistent findings of an increased risk of MM and some NHL subtypes in obese individuals and in persons with autoimmune disease. Relevant to the present application, evidence from both model organism and human occupational studies support the hypothesis that environmental pollutants with carcinogenic and/or immunotoxic effects—such as dioxins and hazardous air pollutants (HAPs)—may be risk factors for MM and/or NHL. However, those studies have many limitations, and most do not assess general population risk from low-dose, passive and possibly chronic exposure to those pollutants or to combinations of multiple pollutants. Geographic information system (GIS)-based modeling of these exposures offers a valid and well accepted tool for examining environmental risk factors for MM, NHL and common histologic subtypes of NHL and could yield novel insights into their etiopathogenesis. The prospective studies proposed in this application will leverage strong investigator expertise and an active collaboration and will include eight large and diverse cohorts, including geocoded residential histories spanning many decades and a projected sample size of ~5,386 incident MM and ~20,354 incident NHL cases. Cox proportional hazard models will be used to examine GIS-modeled passive exposure to dioxins and HAPs (individual and mixtures of pollutants, the latter using quantile G-computation and Bayesian approaches) with known or plausible carcinogenic or immunotoxic properties in relation to risk of MM, NHL, major histologic subtypes and clinically relevant molecular subtypes of diffuse large B-cell lymphoma (DLBCL), an aggressive histologic type of NHL with unknown etiologies. The analyses will incorporate already-harmonized individual-level time-varying risk factor data to assess and control confounding by lifestyle, occupation, demographic and medical history- related risk factors. Additional analyses will assess timing of susceptibility and heterogeneity of observed associations by NHL histologic subtype, calendar period, sex, age, race/ethnicity, body mass index, smoking and socio-demographic and neighborhood contextual factors. The proposed studies have strong potential to yield novel insights on the contribution of passive, low-level exposure to environmental factors to the etiology of MM and NHL, including on risk to individual histologic subtypes of NHL and molecular subtypes of DLBCL, and thus to provide urgently needed identification of novel risk factors for these understudied cancers. |
| Science Code(s)/Area of Science(s) |
Primary: 03 - Carcinogenesis/Cell Transformation Secondary: 03 - Carcinogenesis/Cell Transformation |
| Publications | No publications associated with this grant |
| Program Officer | Abee Boyles |