4.4 Article

Myelodysplastic Syndrome and Benzene Exposure Among Petroleum Workers: An International Pooled Analysis

Journal

JOURNAL OF THE NATIONAL CANCER INSTITUTE
Volume 104, Issue 22, Pages 1724-1737

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/jnci/djs411

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Funding

  1. Conservation for Clean Air and Water Europe (CONCAWE) [EMBSI.940126.L62, 200607010, 200608310, 200609150]
  2. American Petroleum Institute [2003-100820, 2004-202455, 2005-101969]
  3. Aromatic Producers Association
  4. Energy Institute
  5. Australian Institute of Petroleum
  6. Canadian Petroleum Products Institute
  7. American Petroleum Institute via the University of Colorado for studies on benzene in Shanghai, China
  8. Momentive for consultancy and for expert testimony from Univar and Affiliated Holdings, Inc.
  9. ExxonMobil Biomedical Sciences, Inc.
  10. Medical Research Council [G0801056B] Funding Source: researchfish

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Background Benzene at high concentrations is known to cause acute myeloid leukemia (AML), but its relationship with other lymphohematopoietic (LH) cancers remains uncertain, particularly at low concentrations. In this pooled analysis, we examined the risk of five LH cancers relative to lower levels of benzene exposure in petroleum workers. Methods We updated three nested casecontrol studies from Australia, Canada, and the United Kingdom with new incident LH cancers among petroleum distribution workers through December 31, 2006, and pooled 370 potential case subjects and 1587 matched LH cancer-free control subjects. Quantitative benzene exposure in parts per million (ppm) was blindly reconstructed using historical monitoring data, and exposure certainty was scored as high, medium, or low. Two hematopathologists assigned diagnoses and scored the certainty of diagnosis as high, medium, or low. Doseresponse relationships were examined for five LH cancers, including the three most common leukemia cell-types (AML, chronic myeloid leukemia [CML], and chronic lymphoid leukemia [CLL]) and two myeloid tumors (myelodysplastic syndrome [MDS] and myeloproliferative disease [MPD]). Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using conditional logistic regression, controlling for age, sex, and time period. Results Cumulative benzene exposure showed a monotonic doseresponse relationship with MDS (highest vs lowest tertile, > 2.93 vs 0.348 ppm-years, OR 4.33, 95% CI 1.31 to 14.3). For peak benezene exposures (> 3 ppm), the risk of MDS was increased in high and medium certainty diagnoses (peak exposure vs no peak exposure, OR 6.32, 95% CI 1.32 to 30.2) and in workers having the highest exposure certainty (peak exposure vs no peak exposure, OR 5.74, 95% CI 1.05 to 31.2). There was little evidence of doseresponse relationships for AML, CLL, CML, or MPD. Conclusions Relatively low-level exposure to benzene experienced by petroleum distribution workers was associated with an increased risk of MDS, but not AML, suggesting that MDS may be the more relevant health risk for lower exposures.

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