Mesh : Adult Aged Disease-Free Survival Endometrial Neoplasms / drug therapy enzymology metabolism Female Humans Immunohistochemistry Middle Aged Molecular Targeted Therapy / methods Neoplasm Recurrence, Local / drug therapy enzymology metabolism Neoplasms, Hormone-Dependent / drug therapy enzymology metabolism Paraffin Embedding Prognosis Protein Kinase Inhibitors / pharmacology Receptor Protein-Tyrosine Kinases / antagonists & inhibitors biosynthesis Receptors, Estrogen / biosynthesis Receptors, Progesterone / biosynthesis Retrospective Studies Sarcoma, Endometrial Stromal / drug therapy enzymology metabolism Young Adult

来  源:   DOI:10.1016/j.ygyno.2010.12.360   PDF(Sci-hub)

Abstract:
OBJECTIVE: Endometrial stromal sarcoma (ESS) is a rare uterine malignancy. The current treatment approaches yield unsatisfactory results, and potential therapeutic targets need exploration.
METHODS: We reviewed the electronic medical records of 74 patients with low-grade ESS who had been evaluated at the University of Texas MD Anderson Cancer Center between 1995 and 2006. Using immunohistochemistry, we tested the expression of targets in paraffin-embedded tissue samples taken from 13 of the patients.
RESULTS: Forty-seven patients (64%) had a recurrence, and 16 (22%) had died of their disease at last follow-up. The 10-year progression-free survival (PFS) rate was 43% (median PFS duration, 108months), and the overall survival (OS) rate was 85% (median OS, 288months). Patients who received hormonal therapy had an overall response rate of 27%; another 53% had stable disease, with a median time to progression of 24months. No complete response or partial response was observed among patients who received radiotherapy or chemotherapy. In the paraffin-embedded specimens we tested, c-abl was expressed universally. Expression of PDGF-α, PDGF-β, VEGF, and c-Kit was detected in 33%, 36%, 54%, and 8%, of specimens, respectively. EGFR and HER-2 were not detectable in any specimens.
CONCLUSIONS: Our study suggests that ESS is a hormone-dependent malignancy, with hormonal therapy having activity in recurrent disease. Targeted therapy, specifically targeting c-abl may be a potential treatment for this disease.
摘要:
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