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Randomized Dose-Comparative Study of Estrogen Treatment in Postmenopausal Women with ER Positive Metastatic Breast Cancer after Failure of Sequential Endocrine Therapy

Randomized Dose-Comparative Study of Estrogen Treatment in Postmenopausal Women with ER Positive Metastatic Breast Cancer after Failure of Sequential Endocrine Therapy - Estrogen Treatment in Postmenopausal Metastatic Breast Cancer after Failure of Sequential Endocrine Therapy

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002831
Enrollment
60
Registered
2009-12-08
Start date
2009-11-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metastatic breast cancer

Interventions

ethinylestradiol 3mg ethinylestradiol 6mg

Sponsors

Department of Breast and Endocrine Surgery Faculty of Medical and Pharmaceutical Sciences, Kumamoto University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. The case signed informed consent of the patients for the registration 2. The case confirmed by pathological diagnosis 3. postmenopausal women with breast cancer (not less than 50 year old) 4. The case who had progressive disease during the sequential treatments of aromatase inhibitors or SERMs 5. The case with measurable metastatic / recurrent site or evaluable bone metastasis 6. The case with ER positive and/or PgR positive 7. The case that survival more than six months is anticipated 8. The case with PS 0 or 1, additionally the case with PS 2 only by bone metastasis 9. The case with a satisfactory function of a heart/liver/kidney/bone marrow and to satisfy the next condition Hb: more than 8g/dl AST(GOT), ALT(GPT): Less than 2.5 times of the normal value upper limit of the institution

Exclusion criteria

Exclusion criteria: 1. The case with active other malignancies 2. The case with past history of drug allergy or hypersensitivity 3. The case during pregnancy or lactation 4. The case with severe progressive situation with non-indication for the hormone therapy 5. The case judged inappropriate by physicians

Design outcomes

Primary

MeasureTime frame
clinical benefit rate

Secondary

MeasureTime frame
response rate, time to progression, time to treatment failure, adverse events, presictive factor

Countries

Japan

Contacts

Public ContactAyako Okabe

Faculty of Medical and Pharmaceutical Sciences, Kumamoto University Department of Breast and Endocrine Surgery

breast@kumamoto-u.ac.jp096-373-5521

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026