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Search: onr:"swepub:oai:lup.lub.lu.se:5374ff48-06b9-4dc3-ba3c-9ce55ed47a36" > Examestane in advan...

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Examestane in advanced or recurrent endometrial carcinoma: a prospective phase II study by the Nordic Society of Gynecologic Oncology (NSGO)

Lindemann, Kristina (author)
Oslo University Hospital, Norway
Malander, Susanne (author)
Lund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine,University of Lund Hospital, Sweden
Christensen, Rene D. (author)
University of Southern Denmark, Denmark
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Mirza, Mansoor R. (author)
University of Copenhagen Hospital, Denmark
Kristensen, Gunnar B. (author)
Oslo University Hospital, Norway Oslo University Hospital, Norway
Åvall-Lundqvist, Elisabeth (author)
Karolinska Institutet,Östergötlands Läns Landsting,Linköpings universitet,Avdelningen för kliniska vetenskaper,Hälsouniversitetet,Onkologiska kliniken US,Karolinska University Hospital, Sweden
Vergote, Ignace (author)
University Hospital Leuven, Belgium University Hospital Leuven, Belgium
Rosenberg, Per (author)
Östergötlands Läns Landsting,Linköpings universitet,Avdelningen för kliniska vetenskaper,Hälsouniversitetet,Onkologiska kliniken US
Boman, Karin (author)
University Hospital, Sweden
Nordstrom, Britta (author)
Karolinska University Hospital, Sweden
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 (creator_code:org_t)
2014-02-05
2014
English.
In: BMC Cancer. - : Springer Science and Business Media LLC. - 1471-2407. ; 14
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: We evaluated the efficacy and safety of the aromatase inhibitor exemestane in patients with advanced, persistent or recurrent endometrial carcinoma. Methods: We performed an open-label one-arm, two-stage, phase II study of 25 mg of oral exemestane in 51 patients with advanced (FIGO stage III-IV) or relapsed endometrioid endometrial cancer. Patients were stratified into subsets of estrogen receptor (ER) positive and ER negative patients. Results: Recruitment to the ER negative group was stopped prematurely after 12 patients due to slow accrual. In the ER positive patients, we observed an overall response rate of 10%, and a lack of progression after 6 months in 35% of the patients. No responses were registered in the ER negative patients, and all had progressive disease within 6 months. For the total group of patients, the median progression free survival (PFS) was 3.1 months (95% CI: 2.0-4.1). In the ER positive patients the median PFS was 3.8 months (95% CI: 0.7-6.9) and in the ER negative patients it was 2.6 months (95% CI: 2.1-3-1). In the ER positive patients the median overall survival (OS) time was 13.3 months (95% CI: 7.7-18.9), in the ER negative patients the corresponding numbers were 6.1 months (95% CI: 4.1-8.2). Treatment with exemestane was well tolerated. Conclusion: Treatment of estrogen positive advanced or recurrent endometrial cancer with exemestane, an aromatase inhibitor, resulted in a response rate of 10% and lack of progression after 6 months in 35% of the patients.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

Aromatase inhibitor
Exemestane
Endometrial cancer
Treatment
Phase II
study
Aromatase inhibitor; Exemestane; Endometrial cancer; Treatment; Phase II study
MEDICINE

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