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Familial Cancer
 
Fam Cancer. 2010 September; 9(3): 321–325.
Published online 2010 May 5. doi:  10.1007/s10689-010-9344-7
PMCID: PMC2921501

Successful oxytocin-assisted nipple aspiration in women at increased risk for breast cancer

Abstract

The high rate of interval malignancies urges for new screening methods for women at high risk for breast cancer. Nipple aspiration provides direct access to the breast tissue and its DNA, and therefore is a likely candidate, but clinical applications have been limited by the failure to obtain nipple aspiration fluid from most women. We performed oxytocin-assisted nipple aspiration in 90 women at increased risk for breast cancer based on family history or genetic test results (n = 63) and/or previous breast cancer (n = 34). Nipple fluid was obtained from 81/90 women (90%) and bilaterally in 77%. Mean discomfort rating was 0.6 (on a 0–10 scale), which was significantly lower than for mammography or MRI. These findings suggest that a new tool for biomarker detection in oxytocin-assisted nipple fluid of women at high risk for breast cancer is at hand.

Keywords: Nipple aspiration, Breast cancer, BRCA1, BRCA2, Screening, Early detection

Introduction

Breast cancer is the most prevalent cancer for women in the Western world, accounting for 519,000 deaths worldwide each year [1]. Approximately one in eight women will eventually develop breast cancer, but for some women this risk is even higher. A hereditary predisposition is the most important risk factor, with a lifetime risk of developing breast cancer up to 80% in women known to carry a BRCA1 or BRCA2 germline mutation [2].

Several screening and prevention options are available to these women, in order to either prevent the development of breast cancer or detect it at an early stage. However, until now, screening programs are only partly effective and in one out of four in high-risk women interval malignancies are detected [3]. Prophylactic mastectomy and salpingo-oophorectomy have been proven to effectively decrease the risk in women at high risk, but the morbidity associated with this procedure discourages many women to choose this option.

A screening method that gives access to the tissue in which breast cancer arises could add value to the existing methods and increase the rate of breast cancer detection at an early stage [4]. Nipple Aspirate Fluid (NAF), containing breast epithelial cells, free DNA, secreted proteins and hormones is produced in the breast ducts of non-lactating women. In the last decades, multiple techniques have been developed to obtain this fluid, such as non-invasive nipple aspiration, ductal lavage and Random Periareolar Fine Needle Aspiration (RPFNA). Nipple aspiration was previously reported to be only feasible in a small part of the population [5, 6]. The other two techniques showed higher success percentages, but their invasive nature is a serious drawback.

From a previous pilot study we reported that, using oxytocin nasal spray, we were able to obtain nipple fluid in 94% out of 67 healthy volunteers, of which 75% yielded fluid bilaterally [7]. The procedure was very well tolerated. Here we report the initial results of a prospective study on oxytocin-assisted nipple aspiration in women with a moderate to high breast cancer risk.

Materials and methods

Study population

This study is part of a project that aims to explore the possibilities of monitoring development of epigenetic changes in nipple aspirates, with the ultimate goal to optimally schedule preventive (or refrain from) breast surgery in high-risk women. To this end we are assessing promoter hypermethylation in nipple aspirates of high-risk women, of which some will undergo preventive or therapeutic surgery. This will enable assessing the correlation between methylation patterns and the development of (pre)malignant lesions in this group. Oxytocin-assisted nipple aspiration is performed annually. Besides, participants will undergo regular radiological and/or clinical examination as they were used to. Timing of breast surgery will be agreed between patient and oncologist based on usual clinical and radiological findings, blinded to the results of the nipple aspirate analyses. The study protocol of this study was approved by the Hospital’s Ethics Committee and written informed consent was obtained from all participants. This report is a summary of the baseline nipple aspiration experience of the first 90 subjects enrolled between August 2008 and July 2009.

Eligibility criteria

Women were considered at increased risk and included in this study if they were carriers of a BRCA1 or BRCA2 germline mutation, had a pedigree-based risk ≥20%, or had a history of Ductal Carcinoma in Situ (DCIS) or invasive breast cancer. Pregnancy and bilateral mastectomy were exclusion criteria. We did not exclude women that previously underwent other forms of breast surgery, radiotherapy, chemotherapy or hormonal treatment.

Nipple aspiration procedure

Anesthetic cream (Emla) was applied onto the nipple while the breasts were warmed for 10 min. The subjects were administered 4 IE of oxytocin into both nostrils. The nipple was gently wiped with a dekeratinizing agent in order to remove keratin plugs and subsequently cleansed with ethanol. A suction cup (aspirator) was placed over the nipple. Repeated gentle suction by a syringe (10–50 cc) drew fluid to the nipple surface, where droplets were collected by capillary tubes. The entire procedure was repeated at the other breast. Quantitative Multiplex Methylation Specific PCR (QM-MSP) for RASSF1A, SCGB3A1 and APC was performed on 50 randomly selected nipple fluid samples obtained in this study as described before [8].

Questionnaires

A questionnaire, addressing breast cancer risk factors and factors that might influence the success of the procedure was filled out before nipple fluid aspiration. After aspiration participants rated the experienced discomfort during different stages of the procedure and other screening procedures from 0 (“no discomfort at all”) to 10 (“the worst I can imagine”).

Statistical analysis

A paired T-test was used to compare the discomfort scores of different procedures. Fisher’s exact and Chi-square tests were used to examine the association between NAF yielding and potential predictive values. For this analysis, subgroups from Table 1 were pooled because of low numbers. A selection of independent variables (see Table 3) was used in a logistic regression analysis using backward selection procedure, retaining covariates with P ≤ 0.10, for the right and the left breast separately. SPSS 15.0 for Windows was used for statistical analysis, regarding two-sided P ≤ 0.05 as significant.

Table 1
Patient characteristics of 90 patients at increased risk for invasive breast cancer undergoing oxytocin-assisted nipple fluid aspiration
Table 3
Predictive factors for successful oxytocin-assisted nipple aspiration in 90 patients at increased risk for invasive breast cancer undergoing nipple fluid aspiration

Results

A total of 90 women at increased risk were included in this study. Sixty-three women had a family history of breast cancer, six of them were known carriers of a germline BRCA1 mutation and six had a BRCA2 mutation. Twelve women had a history of DCIS and 22 women previously had invasive breast cancer. Participants were 21–72 years old (mean 48 years). All baseline characteristics are shown in Table 1.

The procedure was very well endured. Mean discomfort rating for the total procedure was 0.6, which was significantly lower than breast feeding (1.8), physical examination by a medical oncologist or surgeon (1.1), MRI (2.6) and mammography (4.9; Table 2). No side effects were reported.

Table 2
Discomfort of nipple aspiration compared to other screening procedures for 90 patients at high risk for invasive breast cancer undergoing oxytocin-assisted nipple fluid aspiration

Nipple fluid was obtained from 81 out of 90 women (90%) and bilaterally in 77%. QM-MSP for RASSF1, SCGB3A1 and APC was possible in all 50 samples that we have analyzed. From the 15 women that were known to carry a BRCA1 or BRCA2 mutation or that have family members that are known to be carriers, 14 women yielded bilaterally upon aspiration; in one woman nipple aspiration was only successful in one breast. Characteristics that made women significantly less likely to yield nipple fluid upon aspiration, were not having a family history of breast cancer (P = 0.002), postmenopausal status (P = 0.03) and previous surgery (excision biopsy, breast conserving surgery or other surgery of the breast) on the right side of the breast (P = 0.002; Table 3). Age did not significantly influence the success of the procedure (P = 0.08).

Using logistic regression, no factor could be identified that significantly contributed to the success of nipple aspiration in the left breast in multivariate analysis. For the right breast, only an increased pedigree-related risk (B 2.6; P = 0.02) correlated to the success rate of the aspiration in a multivariate model.

Discussion

Here we describe our findings of performing oxytocin-assisted nipple aspiration in a cohort of 90 high-risk women. We were able to obtain nipple fluid in 90% of high-risk women not selected for age, hormonal factors or previous therapy. A negative effect of surgery of the right breast on NAF yielding was shown, but this effect was not significant in the left breast. Furthermore, in 56% of women that previously underwent surgery of the right breast aspiration was still successful. Therefore, previous surgery is not a reason to exclude women from our study. Similarly, although postmenopausal status and not having a family history for breast cancer decreased the likelihood to yield NAF, 83% of postmenopausal women and 78% of women without a family history of breast cancer still yielded NAF.

A recent article by Loud et al. [9] reported failure to obtain nipple fluid (not supported by oxytocin) in the large majority of women from BRCA families. In this study, only 45 out of 171 women from BRCA families (26%) yielded NAF, 63% (107/171) could have a duct cannulated for ductal lavage, while cytologically evaluable samples were obtained in only 41% of these women. Women without a prior breast cancer history had an increased likelihood of yielding NAF and the presence of NAF was an independent correlate of ductal lavage cell count adequacy. From these data, the authors concluded that ductal lavage is unlikely to be useful in breast cancer screening among BRCA1/2 mutation carriers.

The present study provides quite different results. We believe that vacuum-assisted nipple aspiration, if feasible, is to be preferred over ductal lavage because of its non-invasive nature. Unlike most previous studies, we do not assess cytology, but are focusing on methylation aberrations in our nipple fluid samples. As reported by Loud et al. [9], multiple studies have questioned the reproducibility and clinical value of cytology in nipple fluid. Moreover, Fackler et al. [10] showed that, compared to cytology, analyzing promoter methylation in ductal lavage cells doubled the detection rate of breast cancer. In a previous study, Dooley et al. [11] were able to obtain nipple fluid in a comparable cohort in 84% of women, but in this study only 27% yielded adequate samples for diagnosis.

In conclusion, from our experience oxytocin-assisted nipple aspiration is a very well tolerated non-invasive procedure to obtain nipple fluid in virtually all women, including BRCA1 and BRCA2 mutation carriers. The high success rate of the procedure is not restricted by age, reproductive factors or previous therapy and suggests that a new tool for biomarker detection in nipple fluid of women at increased risk for breast cancer is at hand.

Acknowledgments

Financial support: This work was supported by the Dutch Cancer Society (UU 2007-3977 and UU 2008-4217), the “Integraal Kankercentrum Midden-Nederland (IKMN)”, the “Ata Visser Stichting”, the American Women’s Club of The Hague and A Sister’s Hope/Pink Ribbon.

Conflict of interest statement We declare no conflict of interest for any of the authors.

Open Access This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

Abbreviations

DCIS
Ductal carcinoma in situ
NAF
Nipple aspirate fluid
QM-MSP
Quantitative multiplex methylation specific PCR
RPFNA
Random periareolar fine needle aspiration

References

1. World Health Organization (2009). http://www.who.int/mediacentre/factsheets/fs297/en/index.html Cited 6 Jan 2010
2. King MC, Marks JH, Mandell JB. Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2. Science. 2003;302(5645):643–646. doi: 10.1126/science.1088759. [PubMed] [Cross Ref]
3. Brekelmans CT, Seynaeve C, Bartels CC, et al. Effectiveness of breast cancer surveillance in BRCA1/2 gene mutation carriers and women with high familial risk. J Clin Oncol. 2001;19(4):924–930. [PubMed]
4. Suijkerbuijk KP, Wall E, Vooijs M, Diest PJ. Molecular analysis of nipple fluid for breast cancer screening. Pathobiology. 2008;75(2):149–152. doi: 10.1159/000123853. [PubMed] [Cross Ref]
5. Fabian CJ, Kimler BF, Mayo MS, Khan SA. Breast-tissue sampling for risk assessment and prevention. Endocr Relat Cancer. 2005;12(2):185–213. doi: 10.1677/erc.1.01000. [PubMed] [Cross Ref]
6. Wrensch MR, Petrakis NL, Gruenke LD, et al. Factors associated with obtaining nipple aspirate fluid: analysis of 1428 women and literature review. Breast Cancer Res Treat. 1990;15(1):39–51. doi: 10.1007/BF01811888. [PubMed] [Cross Ref]
7. Suijkerbuijk KP, Wall E, Diest PJ. Oxytocin: bringing magic into nipple aspiration. Ann Oncol. 2007;18(10):1743–1744. doi: 10.1093/annonc/mdm435. [PubMed] [Cross Ref]
8. Fackler MJ, McVeigh M, Mehrotra J, et al. Quantitative multiplex methylation-specific PCR assay for the detection of promoter hypermethylation in multiple genes in breast cancer. Cancer Res. 2004;64(13):4442–4452. doi: 10.1158/0008-5472.CAN-03-3341. [PubMed] [Cross Ref]
9. Loud JT, Thiebaut ACM, Abati AD, et al. Ductal lavage in women from BRCA1/2 families: is there a future for ductal lavage in women at increased genetic risk of breast cancer? Cancer Epidemiol Biomarkers Prev. 2009;18(4):1243–1251. doi: 10.1158/1055-9965.EPI-08-0795. [PMC free article] [PubMed] [Cross Ref]
10. Fackler MJ, Malone K, Zhang Z, et al. Quantitative multiplex methylation-specific PCR analysis doubles detection of tumor cells in breast ductal fluid. Clin Cancer Res. 2006;12(11):3306–3310. doi: 10.1158/1078-0432.CCR-05-2733. [PubMed] [Cross Ref]
11. Dooley WC, Ljung BM, Veronesi U, et al. Ductal lavage for detection of cellular atypia in women at high risk for breast cancer. J Natl Cancer Inst. 2001;93(21):1624–1632. doi: 10.1093/jnci/93.21.1624. [PubMed] [Cross Ref]

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