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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01509625
Other study ID # MIB-FUL-2011-01
Secondary ID
Status Recruiting
Phase N/A
First received December 29, 2011
Last updated August 20, 2013
Start date January 2012
Est. completion date March 2014

Study information

Verified date August 2013
Source Hospital Clinico Universitario San Cecilio
Contact Isabel Blancas, MD
Phone +34958-023609
Email blancaslb@hotmail.com
Is FDA regulated No
Health authority Spain: Agencia Española de Medicamentos y Productos Sanitarios
Study type Observational

Clinical Trial Summary

This retrospective observational study is designed to assess the response to treatment with fulvestrant at a dose of 500 mg/month with a loading dose of 500 mg (LD-500), in terms of progression free survival (PFS), overall survival (OS), and clinical benefit rate (CBR), in post-menopausal women with Advanced Breast Cancer and estrogen receptor positive, who were treated with this medicinal product and at said dose after having progressed with a previous anti-estrogen therapy. During this study, a retrospective data collection will be carried out using the information contained in the Clinical History of said patients, provided that the treatment with fulvestrant at a dose of 500 mg and LD-500.


Description:

Based on the results of the CONFIRM Study, a centralised change in the dosage of Faslodex® to 500 mg/month, with an additional pre-loading dose of 500 mg fourteen days after treatment smart was authorised in Europe; the dose is indicated for the treatment of post-menopausal women with ABC, hormone receptor positive and whose disease had progressed after anti-estrogen therapy.

Several sites worldwide participated in this study, but given the importance of the results obtained and their impact, we believe it is important to have local data available in Spain that would enable us to determine how this new 500 mg dose of Faslodex® behaves in the treatment and to assess treatment response within standard clinical practice and the current indications of this drug.

Therefore, we designed this retrospective, observational study in which we will measure response in term of PFS using data collected from the Clinical History.

Likewise, other variables will be studied: OS, CBR, duration of clinical benefit, tolerability and safety. Patient subgroups, like those who over-express her-2, according to levels of ki-67 and the presence or not of visceral metastases will also be studied.

This retrospective observational study is designed to assess the response to treatment with fulvestrant at a dose of 500 mg/month with a loading dose of 500 mg (LD-500), in terms of progression free survival (PFS), overall survival (OS), clinical benefit rate (CBR), and duration of clinical benefit (DCB, in post-menopausal women with Advanced Breast Cancer and estrogen receptor positive, who were treated with this medicinal product and at said dose after having progressed with a previous anti-estrogen therapy. During this study, a retrospective data collection will be carried out using the information contained in the Clinical History of said patients, provided that the treatment with fulvestrant at a dose of 500 mg and LD-500, had occurred at some point between 1 January 2010 and 31 October 2011 (hereinafter, the study period).

Thus, we will obtain the PFS, OS and CBR data, as well as information on safety and tolerability.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date March 2014
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Signed Informed Consent from patients when possible.

- In the event of patients who are deceased at the time of inclusion, no signed informed consent will be available; thus, the investigator assumes the responsibility of data protection and confidentiality and of safeguarding the processing of the data.

- Post-menopausal women.

- Diagnosed with locally advanced or Metastatic Breast Cancer with histological/cytological confirmation.

- Documented estrogen receptor positive status for the primary tumour.

- Patient who, after progression with a previous anti-estrogen treatment, received treatment at some time with fulvestrant (Faslodex®) at the 500 mg/month and LD-500 dose during the study period.

Exclusion Criteria:

- Having received treatment with unapproved or experimental drugs during the study period.

- Presenting another concomitant cancer other than stage I cervical cancer or cutaneous tumours without lymph node or distant involvement.

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Spain Hospital Torrecardenas Almería Almería
Spain Hospital San Cecilio Granada
Spain Hospital Universitario Virgen de las Nieves Granada
Spain Complejo Hospitalario de Jaén Jaén
Spain Hospital SAS Jeréz de la Frontera Jeréz de la Frontera
Spain Hospital Carlos Hayas Málaga
Spain Hospital Costa del Sol Marbella

Sponsors (1)

Lead Sponsor Collaborator
Isabel Blancas

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Progression Free Survival Response to treatment with fulvestrant (Faslodex®) in terms of Progression Free Survival 22 months No
Secondary Clinical Benefit Rate Response to treatment with fulvestrant in terms of Clinical Benefit Rate 22 months No
Secondary Overall Survival Response to treatment with fulvestrant in terms of Overall Survival 22 months No
Secondary Duration of Clinical Benefit Response to treatment with fulvestrant in terms of Duration of the Clinical Benefit 22 months No
Secondary Number of Participants with Adverse Events 22 months Yes
Secondary Response to treatment with fulvestrant in terms of PFS, CBR, ORR, OS and DCB in a subgroup of patients with visceral metastases and without visceral metastases Response to treatment with fulvestrant at the 500 mg/month and LD 500 dose in terms of PFS, CBR, OS and DCB in a subgroup of patients with visceral metastases and without visceral metastases 22 months No
Secondary Response to treatment with fulvestrant in terms of PFS, CBR, ORR, OS and DCB in a subgroup of patients after a first-line hormonal therapy prior and in subgroup of patients after two or more prior lines of hormonal therapy To assess the response to treatment with fulvestrant (Faslodex®) at the 500 mg/month and LD-500 dose in terms of PFS, CBR, ORR, OS and DCB in a subgroup of patients after a first-line hormonal therapy prior and in subgroup of patients after two or more prior lines of hormonal therapy, and compare both groups 22 months No
Secondary Response to treatment with fulvestrant in terms of PFS, CBR, ORR, OS and DCB in subgroups of patients with her-2 overexpression and those who do not over-express her-2 To assess the response to treatment with fulvestrant at the 500 mg/month and LD 500 dose in terms of PFS, CBR, OS and DCB in subgroups of patients with her-2 overexpression (+++ by immunohistochemistry or FISH positive) and those who do not over-express her-2 and to compare both groups 22 months No
Secondary Response to treatment with fulvestrant in terms of PFS, CBR, ORR, OS and DCB in a subgroup of patients with elevated ki-67 and with low ki-67 To assess the response to treatment with fulvestrant (Faslodex®) at the 500 mg/month and LD-500 dose in terms of PFS, CBR, OS and DCB in a subgroup of patients with elevated ki-67 (greater than or equal to 20%) and with low ki-67 and to compare both groups 22 months No