Abstract

BackgroundCancer research is a national and international priority, with the efficiency and effectiveness of current anti-tumor therapies being one of the major challenges with which physicians are faced.ObjectiveTo assess the impact of exposure to tobacco smoke, arsenic, and phthalates on cervical cancer treatment.MethodsWe investigated 37 patients with locally advanced cervical carcinoma who underwent chemotherapy and radiotherapy. We determined cotinine and five phthalate metabolites in urine samples collected prior to cancer treatment, by gas chromatography coupled to mass spectrometry, and urinary total arsenic by atomic absorption spectrometry with hydride generation. We used linear regression to evaluate the effects of cotinine, arsenic, and phthalates on the change in tumor size after treatment, adjusted for confounding variables.ResultsWe detected no significant associations between urinary cotinine, arsenic, or phthalate monoesters on change in tumor size after treatment, adjusted for urine creatinine, age, baseline tumor size, and cotinine (for arsenic and phthalates). However, higher %mono-ethylhexyl phthalate (%MEHP), a putative indicator of phthalate diester metabolism, was associated with a larger change in tumor size (β = 0.015, 95% CI [0.003–0.03], P = 0.019).ConclusionWe found no statistically significant association between the urinary levels of arsenic, cotinine, and phthalates metabolites and the response to cervical cancer treatment as measured by the change in tumor size. Still, our results suggested that phthalates metabolism may be associated with response to treatment for locally advanced cervical cancer. However, these observations are preliminary and will require confirmation in a larger, more definitive investigation.

Highlights

  • Cervical cancer is among the leading causes of cancer-related morbidity in women worldwide; in 2012 there were 4,343 new cases in Romania alone, accounting for 1,909 deaths (Ferlay et al, 2013)

  • The highest maximum values were measured for mono-butyl phthalate (MBP) (295.5 μg/g) and monobenzyl phthalate (MBzP) (182.9 μg/g), whereas the other phthalates metabolites had lower maximum levels: mono-(2ethylhexyl) phthalate (MEHP) (91.9 μg/g), mono-(2-ethyl-5-oxo-hexyl) phthalate (MEOHP) (34.1 μg/g), and mono-(2-ethyl-5-hydroxyhexyl) phthalate (MEHHP) (88.6 μg/g)

  • We evaluated the impact of exposure to tobacco smoke, arsenic, and phthalates on locally advanced cervical cancer treatment using urine biomarkers from 37 women aged 26– 76 years

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Summary

Introduction

Cervical cancer is among the leading causes of cancer-related morbidity in women worldwide; in 2012 there were 4,343 new cases in Romania alone, accounting for 1,909 deaths (Ferlay et al, 2013). Response to treatment consisting of radiotherapy combined with cisplatin-based chemotherapy in late stages, in most cases of locally advanced cervical cancers, is good, 5-year free survival rates are unsatisfactory (Eifel et al, 2009). Arsenic triggered oncogenesis leads to immune suppression, further facilitating tumor growth and generating a positive feedback loop between cancer and immune function (Acharya et al, 2010) that may impact the effectiveness of treatment. To assess the impact of exposure to tobacco smoke, arsenic, and phthalates on cervical cancer treatment. We used linear regression to evaluate the effects of cotinine, arsenic, and phthalates on the change in tumor size after treatment, adjusted for confounding variables

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