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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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

Other trials in United States

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.

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 groups in NCT00471276
Study groupRoleWhat they receive
1ExperimentalNot described
Receives: Drug: sunitinib

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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)
  1. 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

  2. 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

  3. 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

  4. 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

  5. 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)

  6. 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

  7. 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

  8. 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

  9. 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

  10. 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

  11. 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

  12. 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

  13. 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

  14. 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

  15. 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

  16. 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

  17. 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

  18. 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.

  1. First posted9 May 2007 (estimated)
  2. Study startAug 2007
  3. Primary completionJun 2010
  4. Study completionJun 2010

Resources

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)
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
Data monitoring committee
Yes

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.

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