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Letrozole may be a valuable maintenance treatment in high-grade serous ovarian cancer patients

Authors :
G. Singer
Viola Heinzelmann-Schwarz
S. Stadlmann
Marcus Vetter
Kenneth J. Russell
Francis Jacob
Andreas Schoetzau
Michael Friedlander
A. Knipprath Mészaros
Source :
Gynecologic Oncology. 148:79-85
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

Objectives Endocrine therapy is used as maintenance in estrogen receptor (ER) positive breast cancers and has been proposed in low-grade serous ovarian cancers (LGSOC). Here we examine a rationale for its use as maintenance in high-grade serous ovarian cancers (HGSOC). Methods We accessed the TCGA PANCAN dataset to evaluate the expression of ESR1 . ESR1 expression data on all cancers (n=8901) and HGSOC (n=527) were followed by investigation of ER expression via immunohistochemistry (IHC) (n=4071). The same was performed in an independent cohort for matched primary and recurrent HGSOC (n=80). Finally, newly diagnosed ER+ HGSOC patients were offered a maintenance therapy with Letrozole. Results ESR1 was strongly expressed in similar levels in HGSOC as in breast cancer. We found a strong ER expression via IHC in both the primary and matched recurrent HGSOC, particularly in the Platinum-resistant subgroup. The additional use of Letrozole as maintenance treatment was associated with a significantly prolonged recurrence free interval (after 24months 60% when taking Letrozole versus 38.5% in the control group; p =0.035; RFS: IC 50 reached by one subject versus 13.2months). This effect was also present in patients treated additionally with Bevacizumab; 20.8% of patients had no recurrence after 12months compared to 87.5% when taking Letrozole in addition to Bevacizumab ( p =0.026). Conclusions Primary HGSOC have a slightly higher ESR1 than and a similar ER expression breast cancer where aromatase inhibitor maintenance is routine for decades. Here we demonstrate evidence for the usefulness of Letrozole in HGSOC, particularly in patients with chemotherapy resistance or residual disease.

Details

ISSN :
00908258
Volume :
148
Database :
OpenAIRE
Journal :
Gynecologic Oncology
Accession number :
edsair.doi.dedup.....cebeb56b97a4dd1187ac9534174b2418
Full Text :
https://doi.org/10.1016/j.ygyno.2017.10.036