Metastatic Breast CancerBREASTNCT05559528
BRaziLian outcomE for metAStatic breasT Cancer
An observational study of Metastatic Breast Cancer and Breast Cancer Stage IV, run by Hospital do Coracao at 1 site in Brazil.
Trial summary
Given the certain benefit in efficacy of adding CDK 4/6 inhibitor to first line endocrine therapy in metastatic breast cancer HR+ HER2- , the aim of this project is to evaluate whether patients without private health insurance may have worse outcomes than privately insured women due to limited access to such class of… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Metastatic Breast Cancer, Breast Cancer Stage IV
- How many people
- 300 participants
- Where
- 1 siteBrazil
- Study dates
- 13 Sep 2021to 31 Dec 2024
- How long will I take part?
- 2 Years
- Phase
- Observational
- Are there results?
- None posted in the registry
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
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: - Patients with HR+ HER2 metastatic breast cancer divided into two groups: public health system and private service. Patients will be recruited from 20 cancer treatment centers (10 public and 10 private), chosen in different regions of Brazil. We estimate recruiting 20 patients from each private center and 40 patients from each public center, totaling 300 patients in the survey.
Who may be able to join
- Women may be premenopausal or postmenopausal
- Metastatic advanced breast cancer
- ER-positive and/or PR-positive, HER2-negative tumor
- Eastern Cooperative Oncology Group (ECOG) performance status 0, 1, 2 and 3.
- Start of first-line treatment from 2019
Who cannot join
- Localized or locally advanced disease
- Lack of information about hormonal receptor and HER2 status
- Breast cancer in men
- Breast cancer in pregnancy
- Have progressed from initiation of first-line treatment to study enrollment
Trial locations and contacts
1 site in 1 country.
Brazil1 site, 1 recruiting
- Recruiting
Hcor
São Paulo, São Paulo, 04004-030
Vanessa M Sanvido, Phd, 551130536611, dravanessasanvido@gmail.com
Vanessa M Sanvido, PhD
About this study
Official title: Clinical Outcomes of Breast Cancer and Its Relation With Access to Health Care in Brazil: a Prospective Study in HER2-negative/Hormone Receptor-Positive Metastatic Disease
Given the certain benefit in efficacy of adding CDK 4/6 inhibitor to first line endocrine therapy in metastatic breast cancer HR+ HER2- , the aim of this project is to evaluate whether patients without private health insurance may have worse outcomes than privately insured women due to limited access to such class of drugs during their treatments. Prospective observational study with 300 patients divided into two groups, one with patients from the public health system and the second with patients treated in the private service. Patients will be recruited in different regions of Brazil and will be followed for 24 months, stratified according to the use or not of the CDK 4/6 inhibitors.
Read the detailed description
In Brazil, breast cancer is the most common carcinoma in women, non- melanoma skin carcinomas. 66,280 new cases of breast cancer were estimated for each year of the 2020-2022 triennium, which represents 29.7% of all cancers. It is the main cause of cancer death in women and mortality rates remain high due to the large number of cases diagnosed in advanced stages (around 40%).
According to data from Concord-3, five-year survival estimates in the country were 75.2% (73.9 - 76.5) for the period from 2010 to 2014. However, the 5-year survival rate in the same period was over 85% in 25 countries and reached approximately 90% in North America and Oceania (3). The survival rate in low- and middle-income countries is remarkably different.
This disparity in survival reflects the unequal access of the population to breast screening, difficulty in diagnosis, delayed treatment and limited access to first-line systemic therapy for advanced and metastatic tumors.
Notwithstanding, with the development of new, expensive drugs, breast cancer survival differences between Brazil and high-income countries may increase if the access to new agents is not assured.
One of the most important changes in the hormone positive breast cancer, recently identified, was the greatly increased function of proteins that stimulate cells to grow and multiply, known as CDK4 and 6 (Cyclin-Dependent Kinase). These are normal parts of the human cell, but in this type of tumor they work much faster than they should, making the tumor grow.
Recent studies showed benefit with new target therapies that lower recurrence and progression, as cyclin-dependent kinases 4 and 6 (CDK 4/6) inhibitors with endocrine therapies in hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)- negative advanced breast cancer has shown substantial improvements in progression- free survival (PFS).
Palbociclib (IBRANCE®) is a first-in-class oral inhibitor of cyclin-dependent kinases 4 and 6 that blocks G1-to S-phase progression. There is a strong in-vitro and clinical evidence suggesting that the dual inhibition of CDK 4/6 and ER signaling is a highly effective therapeutic strategy in HR+ MBC. In the phase 2 PALOMA-1 trial, the addition of palbociclib to letrozole significantly improved progression-free survival in women with advanced estrogen receptor-positive and HER2-negative breast cancer. Subsequently, in the phase III trial that included postmenopausal patients with metastatic, HR-positive, HER2-negative breast cancer who had not received prior treatment for advanced disease, an improvement in PFS (24.8 vs. 14.5 months; hazard ratio [HR] 0.58, 95% CI 0.46-0.72) and objective response rate (ORR; 42 vs. 35 percent) was seen with the combination of palbociclib and letrozole compared with letrozole alone.
The National Comprehensive Cancer Network (NCCN) Panel recommends first line therapy for HR-positive HER2-negative with aromatase inhibitor (AI) in combination with CDK 4/6 inhibitor (palbociclib, ribociclib, or abemaciclib) in postmenopausal women or premenopausal women receiving ovarian ablation or ovarian function suppression with an LHRH agonist, combinations of aromatase inhibitors with CDK 4/6 inhibitors (8). However, the situation is rather different in many countries, including Brazil, where the population has limited access to these medications.
The health system in Brazil is organized in two types of assistance: the public system, known as Unified Health System (SUS), where the policies and costs are regulated by the State, and a private system, where the coverage is regulated by the National Supplementary Health Agency (ANS) through agreements with health insurance plans. Nowadays, 75% of the Brazilian population is attended by the public system versus 25% in the Supplementary Health Service.
The commercialization of CDK 4/6 inhibitors was only released in the national territory in 2018, but until nowadays it is not accessible for the majority of patients. Of note, patients in the public health system do not gain access to this class of drugs and those with private insurances usually settle a lawsuit to obtain the treatment once CDK 4/6 inhibitors are not covered by the National Supplementary Health Agency.
Thus, the disparity in the access to these important treatments due to socioeconomic differences probably results in worse outcomes according to health care coverage.
- Conditions
- Metastatic Breast Cancer, Breast Cancer Stage IV
- Keywords
- Breast Cancer, ER+/HER2-
- Medical subject headings
- Breast Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Public health system | Group with patients treated in the public health system in Brazil. They will be stratified according to whether or not CDK 4/6 inhibitors are used in therapy. | |
| Private health system | Group with patients treated in the private health system in Brazil. They will be stratified according to whether or not CDK 4/6 inhibitors are used in therapy. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Progression-free survival (PFS)
Progression-free survival (PFS) is the time from the start of treatment to the date of event defined as the first documented progression or death due to any cause. According to RECIST criteria, progressive disease is defined as at least a 20% increase in the sum of diameter of all measured target lesions, taking as reference the smallest sum of diameter of all target lesions recorded at or after baseline. In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of at least 5 mm. The appearance of one or more new lesions is also considered progression.
Measured: 2 years
Secondary outcomes (3)
Overall Survival (OS)
Overall Survival (OS) is defined as the time from the date of first dose to the date of death due to any cause. Time Frame: Baseline up to approximately 36 months
Measured: 2 years
Cost-effectiveness analysis (CEA)
Cost-effectiveness analysis (CEA) will be measured according to criteria of the World Health Organization. The direct medical costs used in the model will be the weighted average of the costs of the various procedures according to the perspective: a) SUS perspective: the DATASUS, SIGTAP, health price database and CMED price list will be considered e b) Supplementary Health Perspective - the ANS database and CMED price list will be considered
Measured: 2 years
EQ-5D questionnaire
Quality of life will be evaluated by EQ-5D questionnaire is designed for self-completion and, as such, captures information directly from the respondent,however, in this research the questionnaire will be applied by telephone contact.
Measured: 2 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 Sep 2022
- Study start13 Sep 2021
- Primary completion31 Dec 2024 (estimated)
- Study completion31 Dec 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Metastatic Breast CancerStudies of the same condition, open and under way.
- 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
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 300 participants (estimated)
- Target duration
- 2 Years
Sponsor and investigators
- Lead sponsor
- Hospital do Coracao
- Sponsor type
- University, hospital or other
- Collaborators
- Pfizer
- Responsible party
- Sponsor
- Investigators
- Vanessa M Sanvido, PhD, Principal investigator, Hospital do CoracaoAfonso CP Nazário, Professor, Principal investigator, Hospital do CoracaoLuciola B Pontes, MD, Principal investigator, Hospital do Coracao
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05559528
- Sponsor's protocol ID
- BREAST
- Acronym
- BREAST
- Status last verified
- Sep 2022
- First submitted
- 26 Sep 2022
- Last updated
- 29 Sep 2022
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Sanvido VM, Pontes LB, Machado RH, Gomes JO, Barbante LG, Nicola ML, Tokunaga SM, Miranda TA, Laranjeira LN, Negrelli KL, Valeis N, Moutinho MSP, Helber HA, Sa RDS, Kawano-Dourado L, Cavalcanti AB, Nazario ACP. Study protocol to assess clinical outcomes of breast cancer and its relationship with access to healthcare in Brazil-BREAST trial (BRaziLian outcomE for metAStatic breasT cancer): a prospective observational study in HER2-negative/hormone receptor-positive metastatic disease. BMJ Open. 2025 Jun 30;15(6):e087877. doi: 10.1136/bmjopen-2024-087877.
PubMed 40588378
Study at a glance
From the registry record, last updated by the sponsor on 29 Sep 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical Outcomes of Breast Cancer and Its Relation With Access to Health Care in Brazil: a Prospective Study in HER2-negative/Hormone Receptor-Positive Metastatic Disease
- ClinicalTrials.gov ID
- NCT05559528
- Acronym / sponsor ID
- BREAST / BREAST
- Conditions
- Metastatic Breast Cancer, Breast Cancer Stage IV
- Keywords
- Breast Cancer, ER+/HER2-
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 300 participants (estimated)
- Lead sponsor
- Hospital do CoracaoUniversity, hospital or other
- Collaborators
- Pfizer
- Study start
- 13 Sep 2021 (actual)
- Primary completion
- 31 Dec 2024 (estimated)
- Study completion
- 31 Dec 2024 (estimated)
- First posted
- 29 Sep 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Given the certain benefit in efficacy of adding CDK 4/6 inhibitor to first line endocrine therapy in metastatic breast cancer HR+ HER2- , the aim of this project is to evaluate whether patients without private health insurance may have worse outcomes than privately insured women due to limited access to such class of drugs during their treatments. Prospective observational study with 300 patients divided into two groups, one with patients from the public health system and the second with patients treated in the private service. Patients will be recruited in different regions of Brazil and will be followed for 24 months, stratified according to the use or not of the CDK 4/6 inhibitors.
Detailed description
In Brazil, breast cancer is the most common carcinoma in women, non- melanoma skin carcinomas. 66,280 new cases of breast cancer were estimated for each year of the 2020-2022 triennium, which represents 29.7% of all cancers. It is the main cause of cancer death in women and mortality rates remain high due to the large number of cases diagnosed in advanced stages (around 40%).
According to data from Concord-3, five-year survival estimates in the country were 75.2% (73.9 - 76.5) for the period from 2010 to 2014. However, the 5-year survival rate in the same period was over 85% in 25 countries and reached approximately 90% in North America and Oceania (3). The survival rate in low- and middle-income countries is remarkably different.
This disparity in survival reflects the unequal access of the population to breast screening, difficulty in diagnosis, delayed treatment and limited access to first-line systemic therapy for advanced and metastatic tumors.
Notwithstanding, with the development of new, expensive drugs, breast cancer survival differences between Brazil and high-income countries may increase if the access to new agents is not assured.
One of the most important changes in the hormone positive breast cancer, recently identified, was the greatly increased function of proteins that stimulate cells to grow and multiply, known as CDK4 and 6 (Cyclin-Dependent Kinase). These are normal parts of the human cell, but in this type of tumor they work much faster than they should, making the tumor grow.
Recent studies showed benefit with new target therapies that lower recurrence and progression, as cyclin-dependent kinases 4 and 6 (CDK 4/6) inhibitors with endocrine therapies in hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)- negative advanced breast cancer has shown substantial improvements in progression- free survival (PFS).
Palbociclib (IBRANCE®) is a first-in-class oral inhibitor of cyclin-dependent kinases 4 and 6 that blocks G1-to S-phase progression. There is a strong in-vitro and clinical evidence suggesting that the dual inhibition of CDK 4/6 and ER signaling is a highly effective therapeutic strategy in HR+ MBC. In the phase 2 PALOMA-1 trial, the addition of palbociclib to letrozole significantly improved progression-free survival in women with advanced estrogen receptor-positive and HER2-negative breast cancer. Subsequently, in the phase III trial that included postmenopausal patients with metastatic, HR-positive, HER2-negative breast cancer who had not received prior treatment for advanced disease, an improvement in PFS (24.8 vs. 14.5 months; hazard ratio [HR] 0.58, 95% CI 0.46-0.72) and objective response rate (ORR; 42 vs. 35 percent) was seen with the combination of palbociclib and letrozole compared with letrozole alone.
The National Comprehensive Cancer Network (NCCN) Panel recommends first line therapy for HR-positive HER2-negative with aromatase inhibitor (AI) in combination with CDK 4/6 inhibitor (palbociclib, ribociclib, or abemaciclib) in postmenopausal women or premenopausal women receiving ovarian ablation or ovarian function suppression with an LHRH agonist, combinations of aromatase inhibitors with CDK 4/6 inhibitors (8). However, the situation is rather different in many countries, including Brazil, where the population has limited access to these medications.
The health system in Brazil is organized in two types of assistance: the public system, known as Unified Health System (SUS), where the policies and costs are regulated by the State, and a private system, where the coverage is regulated by the National Supplementary Health Agency (ANS) through agreements with health insurance plans. Nowadays, 75% of the Brazilian population is attended by the public system versus 25% in the Supplementary Health Service.
The commercialization of CDK 4/6 inhibitors was only released in the national territory in 2018, but until nowadays it is not accessible for the majority of patients. Of note, patients in the public health system do not gain access to this class of drugs and those with private insurances usually settle a lawsuit to obtain the treatment once CDK 4/6 inhibitors are not covered by the National Supplementary Health Agency.
Thus, the disparity in the access to these important treatments due to socioeconomic differences probably results in worse outcomes according to health care coverage.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 2 Years
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Public health system | – | –Group with patients treated in the public health system in Brazil. They will be stratified according to whether or not CDK 4/6 inhibitors are used in therapy. |
| Private health system | – | –Group with patients treated in the private health system in Brazil. They will be stratified according to whether or not CDK 4/6 inhibitors are used in therapy. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- - Patients with HR+ HER2 metastatic breast cancer divided into two groups: public health system and private service. Patients will be recruited from 20 cancer treatment centers (10 public and 10 private), chosen in different regions of Brazil. We estimate recruiting 20 patients from each private center and 40 patients from each public center, totaling 300 patients in the survey.
Key inclusion criteria (5 listed)
- Women may be premenopausal or postmenopausal
- Metastatic advanced breast cancer
- ER-positive and/or PR-positive, HER2-negative tumor
- Eastern Cooperative Oncology Group (ECOG) performance status 0, 1, 2 and 3.
- Start of first-line treatment from 2019
Key exclusion criteria (5 listed)
- Localized or locally advanced disease
- Lack of information about hormonal receptor and HER2 status
- Breast cancer in men
- Breast cancer in pregnancy
- Have progressed from initiation of first-line treatment to study enrollment
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Progression-free survival (PFS)
Time frame: 2 years
Progression-free survival (PFS) is the time from the start of treatment to the date of event defined as the first documented progression or death due to any cause. According to RECIST criteria, progressive disease is defined as at least a 20% increase in the sum of diameter of all measured target lesions, taking as reference the smallest sum of diameter of all target lesions recorded at or after baseline. In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of at least 5 mm. The appearance of one or more new lesions is also considered progression.
3 secondary outcomes
Overall Survival (OS)
Time frame: 2 years
Cost-effectiveness analysis (CEA)
Time frame: 2 years
EQ-5D questionnaire
Time frame: 2 years
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Sep 2022.
- Derived from this study: PubMed 40588378Sanvido VM, Pontes LB, Machado RH, Gomes JO, Barbante LG, Nicola ML, Tokunaga SM, Miranda TA, Laranjeira LN, Negrelli KL, Valeis N, Moutinho MSP, Helber HA, Sa RDS, Kawano-Dourado L, Cavalcanti AB, Nazario ACP. Study protocol to assess clinical outcomes of breast cancer and its relationship with access to healthcare in Brazil-BREAST trial (BRaziLian outcomE for metAStatic breasT cancer): a prospective observational study in HER2-negative/hormone receptor-positive metastatic disease. BMJ Open. 2025 Jun 30;15(6):e087877. doi: 10.1136/bmjopen-2024-087877.
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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.
Vanessa M Sanvido, PhD principal investigator
Hospital do Coracao
Afonso CP Nazário, Professor principal investigator
Hospital do Coracao
Luciola B Pontes, MD principal investigator
Hospital do Coracao
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Metastatic Breast Cancer and Breast Cancer Stage IV, run by Hospital do Coracao at 1 site in Brazil.
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 5 inclusion and 5 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: status not confirmed, as of the sponsor's last update on 29 Sep 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Brazil. 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.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Vanessa M Sanvido, PhD (551138864688, dravanessasanvido@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Progression-free survival (PFS) (time frame: 2 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05559528, which also lists 1 linked publication.
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 29 Sep 2022.