Abstract | BACKGROUND: METHODS: Fourteen locally advanced breast cancers with clinical benefit on fulvestrant (250 mg/month) as first-line primary endocrine therapy had sequential serum bone-specific alkaline phosphatase (BAP), N-terminal propeptide of procollagen type 1 (PINP) and C-terminal telopeptide (CTX) at 0, 1, 6, 12, and 18 months. Mean percentage changes (95% CI) were calculated. RESULTS: Changes from baseline at 1, 6, 12, and 18 months with BAP (3.9-46.8 ng/ml) were +1.5 (-9.8 to +12.9), +2.2 (-22.1 to +26.6), +17.6 (-12.4 to +47.6), +10.8 (-29.9 to +51.7); with PINP (20.6-82.1 ng/ml) were +3.4 (-12.0 to 19.0), +18.8 (-36.7 to +74.2), +47.5 (-21.4 to 116.3), +33.3 (-49.5 to +116.1) and with CTX (0.14-1.35 ng/ml) were +30.8 (0.1 to +61.6), +13.9 (-22.3 to +50.2), +42.9 (-12.7 to +98.5), +45.2 (-28.3 to +118.8). CONCLUSIONS: Long-term (18 months) stability of bone markers may be exploited by using fulvestrant earlier in sequence of endocrine therapies particularly in adjuvant setting in those with pre-existing decreased bone mass.
|
Authors | A Agrawal, R A Hannon, K L Cheung, R Eastell, J F R Robertson |
Journal | Breast (Edinburgh, Scotland)
(Breast)
Vol. 18
Issue 3
Pg. 204-7
(Jun 2009)
ISSN: 1532-3080 [Electronic] Netherlands |
PMID | 19464177
(Publication Type: Controlled Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Antineoplastic Agents
- Biomarkers
- Collagen Type I
- Peptides
- collagen type I trimeric cross-linked peptide
- Fulvestrant
- Estradiol
- Alkaline Phosphatase
|
Topics |
- Aged
- Alkaline Phosphatase
(blood)
- Antineoplastic Agents
(administration & dosage)
- Biomarkers
(blood)
- Bone Density
(drug effects)
- Bone Remodeling
(drug effects)
- Bone Resorption
(chemically induced, prevention & control)
- Breast Neoplasms
(drug therapy)
- Collagen Type I
(blood)
- Estradiol
(administration & dosage, analogs & derivatives)
- Female
- Fulvestrant
- Humans
- Middle Aged
- Peptides
(blood)
- Pilot Projects
- Postmenopause
(blood)
- Treatment Outcome
|