18F-Fluoroestradiol PET Imaging in a Phase II Trial of Vorinostat to Restore Endocrine Sensitivity in ER+/HER2- Metastatic Breast Cancer
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu klinické zkoušky, fáze II, časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
T32 CA009515
NCI NIH HHS - United States
UL1 RR025014
NCRR NIH HHS - United States
P30 CA047904
NCI NIH HHS - United States
P30 CA016520
NCI NIH HHS - United States
P01 CA042045
NCI NIH HHS - United States
PubMed
32591490
PubMed Central
PMC9364869
DOI
10.2967/jnumed.120.244459
PII: jnumed.120.244459
Knihovny.cz E-zdroje
- Klíčová slova
- ER+ breast cancer, FES, estrogen receptors, metastatic breast cancer, vorinostat,
- MeSH
- dospělí MeSH
- estradiol analogy a deriváty MeSH
- lidé středního věku MeSH
- lidé MeSH
- metastázy nádorů MeSH
- nádory prsu diagnostické zobrazování metabolismus patologie MeSH
- počítačové zpracování obrazu MeSH
- pozitronová emisní tomografie * MeSH
- receptor erbB-2 metabolismus MeSH
- receptory pro estrogeny metabolismus MeSH
- senioři MeSH
- vorinostat farmakologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze II MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- 16-fluoroestradiol MeSH Prohlížeč
- ERBB2 protein, human MeSH Prohlížeč
- estradiol MeSH
- receptor erbB-2 MeSH
- receptory pro estrogeny MeSH
- vorinostat MeSH
Histone deacetylase inhibitors (HDACIs) may overcome endocrine resistance in estrogen receptor-positive (ER+) metastatic breast cancer. We tested whether 18F-fluoroestradiol PET imaging would elucidate the pharmacodynamics of combination HDACIs and endocrine therapy. Methods: Patients with ER+/human epidermal growth factor receptor 2 (HER2)-negative metastatic breast cancer with prior clinical benefit from endocrine therapy but later progression on aromatase inhibitor (AI) therapy were given vorinostat (400 mg daily) sequentially or simultaneously with AI. 18F-fluoroestradiol PET and 18F-FDG PET scans were performed at baseline, week 2, and week 8. Results: Eight patients were treated sequentially, and then 15 simultaneously. Eight patients had stable disease at week 8, and 6 of these 8 patients had more than 6 mo of stable disease. Higher baseline 18F-fluoroestradiol uptake was associated with longer progression-free survival. 18F-fluoroestradiol uptake did not systematically increase with vorinostat exposure, indicating no change in regional ER estradiol binding, and 18F-FDG uptake did not show a significant decrease, as would have been expected with tumor regression. Conclusion: Simultaneous HDACIs and AI dosing in patients with cancer resistant to AI alone showed clinical benefit (6 or more months without progression) in 4 of 10 evaluable patients. Higher 18F-fluoroestradiol PET uptake identified patients likely to benefit from combination therapy, but vorinostat did not change ER expression at the level of detection of 18F-fluoroestradiol PET.
Cancer Imaging Program National Cancer Institute Bethesda Maryland
Department of Biostatistics University of Pittsburgh Pittsburgh Pennsylvania
Department of Diagnostic Radiology Oregon Health and Science University Portland Oregon; and
Department of Radiology University of Pennsylvania Philadelphia Pennsylvania
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