Deficits in plasma oestradiol measurement in studies and management of breast cancer
© BioMed Central Ltd 2004
Published: 28 October 2004
The determination of plasma oestradiol has numerous applications in epidemiology, reproductive medicine and breast cancer management. Commercially available analytical methods, which measure the hormone levels without prior purification, have been successfully developed for measuring oestradiol in premenopausal women. The application of these methodologies to the quantification of the very low levels of oestradiol in postmenopausal women is more problematic in terms of accuracy and interpretation. The importance of using appropriate methodology is discussed and illustrated with data demonstrating the disparity in the results obtained when low levels of oestradiol were quantified using direct and indirect methods.
Keywordsimmunoassays oestradiol postmenopausal
Over recent years the measurement of plasma oestrogen levels, particularly oestradiol levels, in postmenopausal women has made important contributions to an improved understanding of the aetiology and treatment of breast cancer. Current studies aim to build on this by determining whether such measurements can be usefully incorporated into the evaluation of breast cancer risk in relation to the implementation of risk reduction strategies.
Plasma oestradiol analysis has also provided a key pharmacodynamic endpoint in the development of inhibitors of aromatase, the enzyme responsible for oestrogen synthesis . These drugs are now recognised as the most effective endocrine agents in postmenopausal breast cancer and are becoming ever more widely used . Studies of the effects of these agents on other body systems and how this relates to oestrogen suppression and the measurement of compliance with aromatase inhibitor treatment require further analysis of oestrogen levels.
Accurate assessment of plasma oestradiol levels is, however, not straightforward. This is most particularly the case in postmenopausal women where the mean untreated levels are approximately 25 pmol/l (7 pg/ml). The problems associated with accurate assessment are, unfortunately, ill-understood and they may lead to erroneous conclusions being made in research studies and routine evaluation in the clinic if inappropriate assays are conducted.
The assessment of oestradiol has until recently not been an important issue in postmenopausal women other than in research laboratories, but it has been essential for the assessment of infertility and of strategies for ovulation induction. Analytical methodologies have thus focused on supplying results in the range of 100–1200 pmol/l as found in normal premenopausal women, or higher still as found during ovulation induction. The estimation of these levels is far less demanding than those in postmenopausal women. Compromises in the methodologies have thus been possible that allow simplicity, automation, precision, the use of small sample volumes and a rapid turn-round. These may generate substantially inaccurate results but in this context this has little detrimental effect on decision-making.
The major compromise has been to conduct the immunoassay on serum or plasma that has not been subject to pretreatments that extract the oestradiol from the sample (e.g. with an organic extractant such as diethyl ether). Extraction of this type was universally employed in the assay of oestradiol (and other plasma steroids) until about 15 years ago and this allowed the analyte to be quantified in a purified form. The application of the newer, so-called direct analytical approaches to the assessment of postmenopausal oestradiol levels can lead to gross and misleading inaccuracies.
The immunoassay is universally used in the routine laboratory assessment of oestradiol. The inaccuracies result largely from two aspects of the immunoassay's application. First, oestradiol binds avidly (association constant, 0.68 × 109 l/mol) to sex hormone binding globulin such that, if antiserum is added directly to plasma samples, the sex hormone binding globulin effectively competes with the antibody for oestradiol. The direct assays attempt to rectify this by adding displacing agents to the analytical reagents. The second problem is the presence in the blood of very high concentrations of water-soluble conjugated steroids, at concentrations that are orders of magnitude above those of oestradiol. These may cross-react to a minor degree with the oestradiol antiserum but their concentration and the sum effect of numerous such compounds can lead to substantial biases. General issues of the matrix of plasma that differ between samples and can only be approximated in assay standards also contribute to error.
There were significant correlations between the pretreatment results obtained with the sensitive extraction assay and those obtained with the other three assays: r = 0.51 for the DSL-39100 kit, r = 0.73 for the Beckman Coulter Access 33540 and r = 0.98 for the DSL-39100 kit after organic extraction.
The results of the present study with the aromatase inhibitor suggest that at least 70% of the oestradiol measured by the two direct assays in postmenopausal women is an artifact. These assays are probably no worse in this respect than other direct immunoassays, and may in fact be better. It should particularly be noted that the Beckman method has a detection limit of 73 pmol/l and that values below this level should be quoted as < 73 pmol/l. The results indicate that the use of direct assays to check compliance of women on aromatase inhibitors or to conduct research studies in postmenopausal women is inappropriate and is likely to give aberrant guidance. Such assays are also not suitable to help distinguish postmenopausal women from premenopausal women; this is occasionally necessary in tamoxifen-treated patients where confounding effects of the drug on gonadotropin levels make these levels unsuitable for the determination of menopausal status.
This variability between methodological approaches obviously did not prevent the Endogenous Hormones and Breast Cancer Collaborative Group from making the very valuable epidemiological observation of the relationship between plasma oestradiol levels and breast cancer risk. Indeed, these methods may be considered satisfactory for some epidemiological purposes where limitations of sample volume may be a major consideration. The methodological limitations almost certainly affected their ability to define accurately the strength of the relationship, however, and will continue to do so if implemented in future studies.
A number of investigators now view this relationship between plasma oestradiol levels and breast cancer risk as one that has important potential for inclusion in algorithms for predicting breast cancer risk, particularly in association with antihormonal strategies for breast cancer prevention . The implementation of such an approach will require the use of accurate, well-validated, rugged assays that operate alongside well-developed risk relationships for different populations. It is possible that new, more definitive nonimmunoassay approaches to the oestradiol assay (e.g. with tandem mass spectrometry) may allow accurate and precise assay of oestradiol . However, when immunoassays are applied it seems inevitable that we will have to employ labour-intensive and inconvenient extraction procedures for the accurate analysis that these new opportunities demand.
The analyses performed in this study were supported by the Daniel and Phyllis Da Costa International Fund for Breast Cancer Prevention.
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