MECCA: Metronomic Capecitabine Plus Aromatase Inhibitor for First Line Treatment in HR(+), Her2(-) Metastatic Breast Cancer
Study Details
Study Description
Brief Summary
The study is designed to compare the clinical benefit following treatment with aromatase inhibitor in combination with metronomic capecitabine versus aromatase inhibitor alone in women with hormone receptor-positive, Her2-negative advanced breast cancer who have not received prior systemic anti-cancer therapies for their advanced/metastatic disease.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 3 |
Detailed Description
Initial endocrine therapy (ET) is a common choice for hormone receptor positive (HR+), HER2 negative (HER2-) metastatic breast cancer (MBC) patients for its good tolerability, low toxicity and durable response. The median time to progression (TTP) of initial ET in HR+, HER2- metastatic patients is about 9 months with aromatase inhibitors (AIs). However, all metastatic patients receiving ET will develop resistance to the conventional endocrine treatments ultimately. So some novel agents, like palbociclib and everolimus, are approved to be effective in improving the efficacy of standard ET. But the fact we have to face is either palbociclib or everolimus is focusing on a single checkpoint of pathway that responsible for resistance of ET. In clinical, there are some patients without an activation of resistance-related pathways have poor response to endocrine therapy. And the mechanisms of resistance to endocrine therapy is complicated and not fully understood. So far, these novel agents have not completely solved the clinical problems of secondary drug-resistance. Maybe a broad spectrum anti-cancer therapy with low toxicity and good tolerability is more practical and promising in the near future. Metronomic chemotherapy is administration of low-dose chemotherapy to induce disease control in metastatic cancer patients, which has low-incidence of adverse effects. More and more evidences showed activity of metronomic therapy in breast cancer. Metronomic therapy with or without endocrine therapy in both metastatic and neoadjuvant setting showed considerable efficacy. Although the concept of combination of chemotherapy and endocrine therapy simultaneously was large abandoned because of previous using tamoxifen and intravenous chemotherapy showing no additional benefit, with better understanding of the biology of endocrine therapy and metronomic chemotherapy, it's worth to evaluate whether endocrine therapy plus low-dose metronomic chemotherapy brings a better clinical benefit rate without sacrificing the quality of patients' life. In this phase III study, we investigate the efficacy and safety of low-dose capecitabine plus AI to treat metastatic HR+, HER2- postmenopausal breast cancer patients.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Capecitabine+Aromatase inhibitor Capecitabine, 625mg/m2, orally twice daily in combination with an aromatase inhibitor (Anastrozole 1 mg, orally once daily or Letrozole 2.5mg, orally once daily or Exemestane 25mg, orally once daily) |
Drug: Capecitabine
Capecitabine, 625mg/m2, orally twice daily (continuously)
Other Names:
Drug: Aromatase Inhibitor
Aromatase Inhibitor (Anastrozole, 1mg, orally once daily or Letrozole, 2.5mg, orally once daily or Exemestane , 25mg, orally once daily)
Other Names:
|
| Active Comparator: Aromatase inhibitor Aromatase inhibitor (Anastrozole 1 mg, orally once daily or Letrozole 2.5mg, orally once daily or Exemestane 25mg, orally once daily) |
Drug: Aromatase Inhibitor
Aromatase Inhibitor (Anastrozole, 1mg, orally once daily or Letrozole, 2.5mg, orally once daily or Exemestane , 25mg, orally once daily)
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Progress-free survival [Baseline up to approximately 20 months]
Time from randomization to the first documentation of objective tumor progression or to death due to any cause.
Secondary Outcome Measures
- Overall Survival [Baseline until death (up to approximately 48 months)]
Time from randomization to date of death due to any cause.
Other Outcome Measures
- Objective Response Rate (ORR) [Baseline up to approximately 20 months]
Objective response is defined as a complete response (CR) or partial response (PR) according to RECIST v.1.1. recorded from randomization until disease progression or death due to any cause.
- Disease Control Rate (DCR) [Baseline up to approximately 20 months]
Disease control is defined as complete response (CR), partial response (PR), or stable disease (SD) ≥24 weeks according to the RECIST version 1.1 recorded in the time period between randomization and disease progression or death to any cause.
- Change From Baseline in Euro Quality of Life (EQ-5D)- Health State Profile Utility [Baseline up to approximately 20 months]
Instrument designed to assess health status in terms of a single index value or utility score.
- Change From Baseline in Functional Assessment od Cancer therapy -Breast (FACT-B) [Baseline up to approximately 20 months]
Instrument designed to assess patient concerns relating to breast cancer
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Adult women with locoregionally recurrent or metastatic disease not amenable to curative therapy
-
Confirmed diagnosis of ER positive/Her2-negative breast cancer
-
No prior systemic anti-cancer therapy for advanced ER+ disease
-
Any menopausal status
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On a luteinizing hormone releasing hormone (LHRH) agonist for at least 28 days, if pre-/peri-menopausal, and willing to switch to goserelin (Zoladex ®) at time of randomization
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Measurable disease defined by RECIST version 1.1, or bone-only disease
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Eastern Cooperative Oncology Group (ECOG) 0-1
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Adequate organ and marrow function
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Resolution of all toxic effects of prior therapy or surgical procedures
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Patient must agree to provide tumor tissue from metastatic tissue at baseline
Exclusion Criteria:
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Patients with advanced, symptomatic, visceral spread that are at risk of life threatening complication in the short term
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Known uncontrolled or symptomatic central nervous system metastases
-
Second primary malignancy(except in situ carcinoma of the cervix or adequately treated nonmelanomatous carcinoma of the skin)
-
Serious uncontrolled intercurrent infections or intercurrent medical or psychiatric illness
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center | Guangzhou | Guangdong | China | 510060 |
Sponsors and Collaborators
- Sun Yat-sen University
Investigators
- Principal Investigator: Shusen Wang, MD, Sun Yat-sen University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- SYSUCC 5010-MECCA