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Effects of aromatase inhibitors and body mass index on steroid hormone levels in women with early and advanced breast cancer
Oleh:
Elliott, K.M.
;
Dent, J.
;
Stanczyk, F.Z.
;
Woodley, L.
Jenis:
Article from Article - diterbitkan di jurnal ilmiah internasional
Dalam koleksi:
BJS: British Journal of Surgery vol. 101 no. 08 (Jul. 2014)
,
page 939-948.
Topik:
aromatase inhibitors
;
breast cancer
;
metastatic disease
;
oestrogen bio synthesis
;
aromatase
;
postmenopausal
Ketersediaan
Perpustakaan FK
Nomor Panggil:
B15.K
Non-tandon:
1 (dapat dipinjam: 0)
Tandon:
tidak ada
Lihat Detail Induk
Isi artikel
Background Aromatase inhibitors (AIs) are central to the management of oestrogen receptor-positive breast cancer in the adjuvant and metastatic setting. Levels of circulating steroid hormones (SHs) were measured in patients established on AIs to investigate: the influence of body mass index (BMI) in both the adjuvant and metastatic setting; the class of AI utilized in the adjuvant setting (steroidal versus non-steroidal); and differences in SH levels between women treated adjuvantly and those receiving a second-line AI for locally advanced/metastatic disease. Methods Plasma levels of androstenedione, 5-androstene-3ß,17ß-diol, dehydroepiandrosterone, oestradiol and testosterone were measured by radioimmunoassay in women with breast cancer who were receiving AIs in either an adjuvant or a metastatic setting. Differences between mean SH levels by class of AI, BMI, and second-line versus adjuvant therapy were assessed. Results Sixty-four women were receiving AI therapy, 45 (70 per cent) in an adjuvant setting and 19 (30 per cent) were taking a second-line AI. There was no significant correlation between BMI and SH levels. However, BMI was significantly higher in the second-line AI cohort compared with the adjuvant cohort (29·8 versus 26·2?kg/m2 respectively; P?=?0·026). In the adjuvant setting, patients receiving a steroidal AI had significantly higher levels of all five hormones (P?0·050). In the second-line AI cohort, oestradiol levels were significantly higher than in the adjuvant cohort (4·5 versus 3·3?pg/ml respectively; P?=?0·022). Multivariable analysis adjusted for BMI confirmed the higher residual oestradiol level in the second-line AI group (P?=?0·063) and a significantly higher androstenedione level (P?=?0·022). Conclusion Residual levels of SH were not significantly influenced by BMI. However, the significant differences in residual SH levels between the second-line and adjuvant AI cohort is of relevance in the context of resistance to AI therapy, and warrants further investigation.
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