Hormone Therapy + Ribociclib for Breast Cancer
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores whether hormone therapy with ribociclib is as effective as chemotherapy followed by the same hormone therapy in treating certain types of breast cancer. Ribociclib, a targeted cancer therapy, blocks enzymes that aid tumor cell growth, while hormone therapy reduces estrogen, which some tumor cells require for growth. Suitable candidates for this trial include postmenopausal women or men with high-stage breast cancer, a low risk of recurrence, and no prior chemotherapy or specific hormone therapies. As a Phase 3 trial, this research represents the final step before FDA approval, offering participants the opportunity to contribute to a potentially groundbreaking treatment.
Do I need to stop my current medications for the trial?
The trial protocol does not specify if you need to stop taking your current medications. However, you must not be using systemic hormone replacement therapy at the time of registration, and if you were, it needs to be stopped with an appropriate washout period (time without taking certain medications).
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that ribociclib, when combined with hormone therapy, is generally safe for treating breast cancer. Most side effects from ribociclib can be managed by adjusting the dose, allowing patients to continue treatment without major problems. One study found that 90.7% of patients taking ribociclib were free from invasive disease after three years.
Hormone therapy, using drugs like letrozole, anastrozole, or exemestane, is also well-tolerated. These treatments work by lowering estrogen levels, which can help slow or stop the growth of some breast cancers. Studies have shown no major safety differences between these drugs, so they are all considered safe options. However, some patients taking exemestane have reported stopping treatment early due to side effects.
Overall, both ribociclib and hormone therapies have been thoroughly studied and are considered safe for many patients.12345Why are researchers excited about this trial's treatments?
Researchers are excited about these treatments for breast cancer because they combine hormone therapy with ribociclib, a CDK4/6 inhibitor that works by blocking specific proteins that help cancer cells grow. Unlike standard treatments that may only involve hormone therapy or chemotherapy, ribociclib adds a targeted approach, aiming to enhance the effectiveness of hormone therapy by interfering with cancer cell division. Additionally, this combination could potentially offer a more tailored treatment approach, targeting cancer cells more precisely and possibly reducing side effects compared to traditional chemotherapy. This unique mechanism gives hope for better outcomes and improved quality of life for patients.
What evidence suggests that this trial's treatments could be effective for breast cancer?
Research has shown that ribociclib, when combined with hormone therapy, improves outcomes for breast cancer patients. In this trial, participants in Arm A will receive chemotherapy, hormone therapy (letrozole, anastrozole, or exemestane), and ribociclib. Participants in Arm B will receive hormone therapy and ribociclib without chemotherapy. One study found that combining ribociclib with letrozole increased the average survival time to nearly 64 months, compared to 51 months with letrozole alone. This finding suggests that ribociclib can extend the lives of breast cancer patients. Hormone therapies like letrozole, anastrozole, and exemestane are also effective, with about 90% of patients surviving for 8 years. These treatments work by lowering estrogen levels, which some breast cancer cells need to grow. Using ribociclib together with these hormone therapies shows promising results in managing breast cancer.12367
Who Is on the Research Team?
Nancy Chan
Principal Investigator
ECOG-ACRIN Cancer Research Group
Are You a Good Fit for This Trial?
This trial is for adults (18+) who are postmenopausal women or men with high-stage breast cancer but a low risk of the cancer coming back. Participants must have had surgery to remove their tumor and meet specific staging criteria, be in reasonably good health, and not need further major lymph node surgery.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Patients receive either chemotherapy followed by hormone therapy with ribociclib or hormone therapy with ribociclib alone
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Anastrozole
- Chemotherapy
- Exemestane
- Letrozole
- Ribociclib Succinate
Trial Overview
The study compares two treatments: one group gets hormone therapy plus ribociclib; the other gets chemotherapy first, then hormone therapy plus ribociclib. The goal is to see if skipping chemo works just as well for this type of breast cancer.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Active Control
Patients receive their physician's choice of standard of care hormone therapy with letrozole, anastrozole, or exemestane PO QD on days 1-28 of each cycle and ribociclib PO QD on days 1-21 of each cycle. Cycles repeat every 28 days for at least 60 months for hormone therapy and up to 3 years for ribociclib, in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan, bone scan, or FDG PET-CT scan and may optionally undergo blood sample collection throughout the study.
Patients receive their physician's choice of standard of care chemotherapy. Patients then receive their physician's choice of standard of care hormone therapy with letrozole, anastrozole, or exemestane PO QD on days 1-28 of each cycle, as well as ribociclib PO QD on days 1-21 of each cycle. Cycles repeat every 28 days for at least 60 months for hormone therapy and up to 3 years for ribociclib, in the absence of disease progression or unacceptable toxicity. Patients also undergo CT scan, bone scan, or FDG PET-CT scan and may optionally undergo blood sample collection throughout the study.
Find a Clinic Near You
Who Is Running the Clinical Trial?
National Cancer Institute (NCI)
Lead Sponsor
Citations
Outcomes of Anastrozole, Letrozole, and Exemestane ... - PMC
This comparative effectiveness research compares disease-free survival and overall survival 5 and 8 years after the initiation of endocrine ...
Outcomes of Anastrozole, Letrozole, and Exemestane in ...
This comparative effectiveness research compares disease-free survival and overall survival 5 and 8 years after the initiation of endocrine ...
3.
cancertherapyadvisor.com
cancertherapyadvisor.com/news/anastrozole-letrozole-os-dfs-versus-exemestane-postmenopausal-hr-early-breast-cancer/Anastrozole, Letrozole Produce Better OS, DFS Versus ...
The 8-year OS rates were 90.1%, 91.7%, and 91.2%, respectively. In the sensitivity analyses, researchers found that chemotherapy increased the ...
Comparative Efficacy and Safety of Adjuvant Letrozole ...
Letrozole did not demonstrate significantly superior efficacy or safety compared with anastrozole in postmenopausal patients with HR-positive, node-positive ...
5.
mdanderson.elsevierpure.com
mdanderson.elsevierpure.com/en/publications/outcomes-of-anastrozole-letrozole-and-exemestane-in-patients-with/Outcomes of Anastrozole, Letrozole, and Exemestane in ...
8-year OS was 88.8% (95% CI, 88.0%-89.6%) for the exemestane group compared with 90.5% (95% CI, 90.2%-90.8%) for the anastrozole group and 89.9%
6.
oncologynurseadvisor.com
oncologynurseadvisor.com/news/anastrozole-letrozole-os-dfs-versus-exemestane-postmenopausal-hr-early-breast-cancer/Anastrozole, Letrozole Produce Better OS, DFS Versus ...
Under perfect persistence, the 8-year DFS rate was 81.0% in the exemestane arm, 82.9% in the anastrozole arm, and 83.1% in the letrozole arm.
Adjuvant aromatase inhibitor therapy: Outcomes and safety
The Anastrozole or Tamoxifen Alone or in Combination (ATAC) trial has compiled safety data for initial adjuvant AI therapy with anastrozole (ANA) versus TAM ...
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