Breast NeoplasmsPhase 2NCT00471276
Efficacy And Safety Of Sunitinib In Women With Advanced Breast Cancer
A Phase 2 study testing sunitinib in people with Breast Neoplasms, run by Pfizer at 31 sites in United States.
Trial summary
Patients with advanced breast cancer to receive sunitinib (Sutent) once daily until disease progression. Read more about this study
- Who is it for?
- Ages 18 years and older, women only
- Conditions the study is for
- Breast Neoplasms
- What is being tested?
- sunitinib
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 83 participants
- Where
- 31 sitesUnited States
- Study dates
- Aug 2007to Jun 2010
- Phase
- Phase 2
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Women only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Histologically or cytologically proven diagnosis of breast cancer
- Metastatic or locally recurrent disease that is, in the opinion of the investigator, not amenable to resection or radiation therapy
- Patients with at least one measurable lesion as per RECIST
Who cannot join
- Inflammatory breast cancer
- Prior treatment with VEGF inhibitors (unless in adjuvant setting at least 12 months ago)
Trial locations and contacts
31 sites in 1 country.
31 sites in 1 country
United States31 sites
Pfizer Investigational Site
Asheville, North Carolina, 28806
Pfizer Investigational Site
Bakersfield, California, 93309
Pfizer Investigational Site
Bismarck, North Dakota, 58501
Pfizer Investigational Site
Boynton Beach, Florida, 33435
Pfizer Investigational Site
Burbank, California, 91505-4866
Pfizer Investigational Site
Chapel Hill, North Carolina, 27599
Pfizer Investigational Site
Columbia, Missouri, 65203
Pfizer Investigational Site
Everett, Washington, 98201
Pfizer Investigational Site
Fountain Valley, California, 92708
Pfizer Investigational Site
Franklin, Tennessee, 37067
Pfizer Investigational Site
Gallatin, Tennessee, 37066
Pfizer Investigational Site
Hawthorne, California, 90250
Pfizer Investigational Site
Hermitage, Tennessee, 37076
Pfizer Investigational Site
Kalamazoo, Michigan, 49007
Pfizer Investigational Site
Kernersville, North Carolina, 27284
Pfizer Investigational Site
Lebanon, Tennessee, 37087
Pfizer Investigational Site
Lexington, North Carolina, 27292
Pfizer Investigational Site
Long Beach, California, 90806
Pfizer Investigational Site
Louisville, Kentucky, 40207
Pfizer Investigational Site
Maple Grove, Minnesota, 55369
Pfizer Investigational Site
Minneapolis, Minnesota, 55454
Pfizer Investigational Site
Minneapolis, Minnesota, 55455
Pfizer Investigational Site
Murfreesboro, Tennessee, 37130
Pfizer Investigational Site
Nashville, Tennessee, 37203
Pfizer Investigational Site
Nashville, Tennessee, 37205
Pfizer Investigational Site
Nashville, Tennessee, 37207
Pfizer Investigational Site
Nashville, Tennessee, 37211
Pfizer Investigational Site
North Wilkesboro, North Carolina, 28659
Pfizer Investigational Site
Smyrna, Tennessee, 37167
Pfizer Investigational Site
Winston-Salem, North Carolina, 27103
Pfizer Investigational Site
Zion, Illinois, 60099
About this study
Official title: A Phase II Study Of Sunitinib Malate Single Agent For The Treatment Of Women With Advanced Breast Cancer
Patients with advanced breast cancer to receive sunitinib (Sutent) once daily until disease progression.
- Conditions
- Breast Neoplasms
- Being tested
- sunitinib
- Keywords
- Metastatic Breast Cancer
- Medical subject headings
- Breast Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
sunitinibDrug
Also called Sutent, sunitinib
sunitinib (Sutent), 37.5 mg, daily dosing
| Study group | Role | What they receive |
|---|---|---|
| 1 | Experimental | Not described Receives: Drug: sunitinib |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of Participants With Objective Response
Number of participants with objective response based assessment of confirmed complete response (CR) or confirmed partial response (PR) according to Response Evaluation Criteria in Solid Tumors (RECIST). CR defined as disappearance of all target lesions. PR defined as a greater than or equal to 30 percent (≥30%) decrease in sum of the longest dimensions of the target lesions taking as a reference the baseline sum longest dimensions.
Measured: Baseline, Week 9, and every 8 weeks up to Month 34
Secondary outcomes (18)
Number of Participants With Clinical Benefit
The sum of participants with confirmed CR, PR, and stable disease (SD) greater than (>) 6 months according to RECIST. SD defined as neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for progressive disease, taking as reference smallest sum of longest dimensions since treatment started.
Measured: Baseline, Week 9, and every 8 weeks up to Month 34
Number of Participants With Objective Response of Superficial Lesions
Number of participants with objective response based assessment of confirmed CR or PR of superficial lesions according to RECIST. Superficial lesions included skin lesions, chest wall lesions, and breast lesions and lymph nodes if followed up by physical examination.
Measured: Baseline, every 4 weeks up to Month 34
Progression-Free Survival (PFS)
Time from date of randomization to date of first documentation of objective tumor progression or death due to any cause, whichever occurred first. PFS calculated as (Months)=(first event date minus randomization date plus 1) divided by 30.4.
Measured: Baseline up to Month 34
Duration of Response (DR)
Time from first objective documentation of complete or partial response that was subsequently confirmed to first documentation of disease progression or death due to any cause, whichever occurred first. DR calculated as (Weeks)=(end date for DR minus first subsequent confirmed CR or PR plus 1) divided by 7.
Measured: Baseline up to Month 34 or early termination
Overall Survival (OS)
Time from randomization to date of death due to any cause. OS (Months)=(death date minus date of first dose of study medication plus 1) divided by 30.4. For participants who were alive, overall survival was censored at last contact.
Measured: Baseline until death (up to Month 34)
Number of Participants With Objective Response for Subgroup of Participants Whom Sunitinib Was at Least a Third Line Therapy
Number of participants with objective response based assessment of confirmed CR or PR according to RECIST. CR defined as disappearance of all target lesions. PR defined as ≥30% decrease in sum of the longest dimensions of the target lesions taking as a reference the baseline sum longest dimensions.
Measured: Baseline, Week 9, and every 8 weeks up to Month 34
Change From Baseline in European Organization for Research and Treatment of Cancer Quality of Life Questionaire-C30 (EORTC- QLQ-C30) Score
EORTC QLQ-C30: included functional scales (physical, role, cognitive, emotional, and social), global health status, symptom scales (fatigue, pain, nausea/vomiting), and single items (dyspnoea, appetite loss, insomnia, constipation/diarrhea, and financial difficulties). Most questions used 4-point scale (1 'Not at All' to 4 'Very Much'); 2 questions used 7-point scale (1 'Very Poor' to 7 'Excellent'). Scores averaged, transformed to 0-100 scale; higher score=better level of functioning or greater degree of symptoms. Change from baseline=Cycle/Day score minus baseline score.
Measured: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ Companion Breast Cancer Module (EORTC-QLQ-BR23) Score: Body Image
EORTC-QLQ-BR23: included functional scales (body image, sexual functioning, sexual enjoyment, and future perspective) and single item symptoms scales (systemic therapy side effects, breast symptoms, arm symptoms, and upset by hair loss). Questions used 4-point Likert scale (1 'Not at All' to 4 'Very Much'). Scores averaged and transformed to 0-100 scale. High score for functional scale=high/healthy level of functioning. High score for single item=high level of symptomatology/problems. Change from baseline=Cycle/Day score minus baseline score.
Measured: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Future Perspective
EORTC-QLQ-BR23: included functional scales (body image, sexual functioning, sexual enjoyment, and future perspective) and single item symptoms scales (systemic therapy side effects, breast symptoms, arm symptoms, and upset by hair loss). Questions used 4-point Likert scale (1 'Not at All' to 4 'Very Much'). Scores averaged and transformed to 0-100 scale. High score for functional scale=high/healthy level of functioning. High score for single item=high level of symptomatology/problems. Change from baseline=Cycle/Day score minus baseline score.
Measured: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Sexual Enjoyment
EORTC-QLQ-BR23: included functional scales (body image, sexual functioning, sexual enjoyment, and future perspective) and single item symptoms scales (systemic therapy side effects, breast symptoms, arm symptoms, and upset by hair loss). Questions used 4-point Likert scale (1 'Not at All' to 4 'Very Much'). Scores averaged and transformed to 0-100 scale. High score for functional scale=high/healthy level of functioning. High score for single item=high level of symptomatology/problems. Change from baseline=Cycle/Day score minus baseline score.
Measured: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Sexual Functioning
EORTC-QLQ-BR23: included functional scales (body image, sexual functioning, sexual enjoyment, and future perspective) and single item symptoms scales (systemic therapy side effects, breast symptoms, arm symptoms, and upset by hair loss). Questions used 4-point Likert scale (1 'Not at All' to 4 'Very Much'). Scores averaged and transformed to 0-100 scale. High score for functional scale=high/healthy level of functioning. High score for single item=high level of symptomatology/problems. Change from baseline=Cycle/Day score minus baseline score.
Measured: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Arm Symptoms
EORTC-QLQ-BR23: included functional scales (body image, sexual functioning, sexual enjoyment, and future perspective) and single item symptoms scales (systemic therapy side effects, breast symptoms, arm symptoms, and upset by hair loss). Questions used 4-point Likert scale (1 'Not at All' to 4 'Very Much'). Scores averaged and transformed to 0-100 scale. High score for functional scale=high/healthy level of functioning. High score for single item=high level of symptomatology/problems. Change from baseline=Cycle/Day score minus baseline score.
Measured: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Breast Symptoms
EORTC-QLQ-BR23: included functional scales (body image, sexual functioning, sexual enjoyment, and future perspective) and single item symptoms scales (systemic therapy side effects, breast symptoms, arm symptoms, and upset by hair loss). Questions used 4-point Likert scale (1 'Not at All' to 4 'Very Much'). Scores averaged and transformed to 0-100 scale. High score for functional scale=high/healthy level of functioning. High score for single item=high level of symptomatology/problems. Change from baseline=Cycle/Day score minus baseline score.
Measured: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Systemic Therapy Side Effects
EORTC-QLQ-BR23: included functional scales (body image, sexual functioning, sexual enjoyment, and future perspective) and single item symptoms scales (systemic therapy side effects, breast symptoms, arm symptoms, and upset by hair loss). Questions used 4-point Likert scale (1 'Not at All' to 4 'Very Much'). Scores averaged and transformed to 0-100 scale. High score for functional scale=high/healthy level of functioning. High score for single item=high level of symptomatology/problems. Change from baseline=Cycle/Day score minus baseline score.
Measured: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Upset by Hair Loss
EORTC-QLQ-BR23: included functional scales (body image, sexual functioning, sexual enjoyment, and future perspective) and single item symptoms scales (systemic therapy side effects, breast symptoms, arm symptoms, and upset by hair loss). Questions used 4-point Likert scale (1 'Not at All' to 4 'Very Much'). Scores averaged and transformed to 0-100 scale. High score for functional scale=high/healthy level of functioning. High score for single item=high level of symptomatology/problems. Change from baseline=Cycle/Day score minus baseline score.
Measured: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in Cancer Therapy Satisfaction Questionnaire (CTSQ) Score: Expectation of Therapy
CTSQ: included 3 multi-item subscales (Expectation of Therapy [ET], Satisfaction with Therapy [SWT], and Feelings about Side Effects [FSE]). Questions used 5-point scale from 1 'Never' to 5 'Always'. Scores averaged and transformed to 0-100 scale, with higher scores associated with better outcomes. Change from baseline=score for Cycle/Day minus baseline score.
Measured: Baseline, Day 15, Week 4 and 8, and every 8 weeks up to Month 36 or early termination
Change From Baseline in CTSQ Score: Feelings About Side Effects
CTSQ: included 3 multi-item subscales (Expectation of Therapy [ET], Satisfaction with Therapy [SWT], and Feelings about Side Effects [FSE]). Questions used 5-point scale from 1 'Never' to 5 'Always'. Scores averaged and transformed to 0-100 scale, with higher scores associated with better outcomes. Change from baseline=score for Cycle/Day minus baseline score.
Measured: Baseline, Day 15, Week 4 and 8, and every 8 weeks up to Month 36 or early termination
Change From Baseline in CTSQ Score: Satisfaction With Therapy
CTSQ: included 3 multi-item subscales (Expectation of Therapy [ET], Satisfaction with Therapy [SWT], and Feelings about Side Effects [FSE]). Questions used 5-point scale from 1 'Never' to 5 'Always'. Scores averaged and transformed to 0-100 scale, with higher scores associated with better outcomes. Change from baseline=score for Cycle/Day minus baseline score.
Measured: Baseline, Day 15, Week 4 and 8, and every 8 weeks up to Month 36 or early termination
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 May 2007 (estimated)
- Study startAug 2007
- Primary completionJun 2010
- Study completionJun 2010
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Breast NeoplasmsStudies of the same condition, open and under way.
- More trials run by PfizerThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 83 participants (actual)
Sponsor and investigators
- Lead sponsor
- Pfizer
- Sponsor type
- Industry (pharma, biotech, devices)
- Investigators
- Pfizer CT.gov Call Center, Study director, Pfizer
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00471276
- Sponsor's protocol ID
- A6181068
- Status last verified
- Jul 2011
- First submitted
- 7 May 2007
- Last updated
- 25 Jul 2011
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 25 Jul 2011. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase II Study Of Sunitinib Malate Single Agent For The Treatment Of Women With Advanced Breast Cancer
- ClinicalTrials.gov ID
- NCT00471276
- Acronym / sponsor ID
- A6181068
- Conditions
- Breast Neoplasms
- Keywords
- Metastatic Breast Cancer
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 83 participants (actual)
- Lead sponsor
- PfizerIndustry (pharma, biotech, devices)
- Study start
- Aug 2007
- Primary completion
- Jun 2010 (actual)
- Study completion
- Jun 2010 (actual)
- First posted
- 9 May 2007 (estimated)
- Results
- Posted 22 Jul 2011
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Patients with advanced breast cancer to receive sunitinib (Sutent) once daily until disease progression.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| 1 | Experimental | Drug: sunitinib |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Histologically or cytologically proven diagnosis of breast cancer
- Metastatic or locally recurrent disease that is, in the opinion of the investigator, not amenable to resection or radiation therapy
- Patients with at least one measurable lesion as per RECIST
Key exclusion criteria (2 listed)
- Inflammatory breast cancer
- Prior treatment with VEGF inhibitors (unless in adjuvant setting at least 12 months ago)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| sunitinibAlso: Sutent, sunitinibsunitinib (Sutent), 37.5 mg, daily dosing | Drug | 1 |
Primary outcome
Number of Participants With Objective Response
Time frame: Baseline, Week 9, and every 8 weeks up to Month 34
Number of participants with objective response based assessment of confirmed complete response (CR) or confirmed partial response (PR) according to Response Evaluation Criteria in Solid Tumors (RECIST). CR defined as disappearance of all target lesions. PR defined as a greater than or equal to 30 percent (≥30%) decrease in sum of the longest dimensions of the target lesions taking as a reference the baseline sum longest dimensions.
18 secondary outcomes
Number of Participants With Clinical Benefit
Time frame: Baseline, Week 9, and every 8 weeks up to Month 34
Number of Participants With Objective Response of Superficial Lesions
Time frame: Baseline, every 4 weeks up to Month 34
Progression-Free Survival (PFS)
Time frame: Baseline up to Month 34
Duration of Response (DR)
Time frame: Baseline up to Month 34 or early termination
Overall Survival (OS)
Time frame: Baseline until death (up to Month 34)
Number of Participants With Objective Response for Subgroup of Participants Whom Sunitinib Was at Least a Third Line Therapy
Time frame: Baseline, Week 9, and every 8 weeks up to Month 34
Change From Baseline in European Organization for Research and Treatment of Cancer Quality of Life Questionaire-C30 (EORTC- QLQ-C30) Score
Time frame: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ Companion Breast Cancer Module (EORTC-QLQ-BR23) Score: Body Image
Time frame: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Future Perspective
Time frame: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Sexual Enjoyment
Time frame: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Sexual Functioning
Time frame: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Arm Symptoms
Time frame: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Breast Symptoms
Time frame: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Systemic Therapy Side Effects
Time frame: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in EORTC-QLQ-BR23 Score: Upset by Hair Loss
Time frame: Baseline, every 4 weeks up to Month 31 or early termination
Change From Baseline in Cancer Therapy Satisfaction Questionnaire (CTSQ) Score: Expectation of Therapy
Time frame: Baseline, Day 15, Week 4 and 8, and every 8 weeks up to Month 36 or early termination
Change From Baseline in CTSQ Score: Feelings About Side Effects
Time frame: Baseline, Day 15, Week 4 and 8, and every 8 weeks up to Month 36 or early termination
Change From Baseline in CTSQ Score: Satisfaction With Therapy
Time frame: Baseline, Day 15, Week 4 and 8, and every 8 weeks up to Month 36 or early termination
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Jul 2011.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- To obtain contact information for a study center near you, click here.Link provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Pfizer CT.gov Call Center study director
Pfizer
31 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing sunitinib in people with Breast Neoplasms, run by Pfizer at 31 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 25 Jul 2011. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 31 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 22 Jul 2011). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of Participants With Objective Response (time frame: Baseline, Week 9, and every 8 weeks up to Month 34). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Jul 2011.