Real-World data may reveal which breast cancer subtype responds best to CDK4/6 inhibitors
NCT ID NCT07704801
First seen Jul 15, 2026 · Last updated Jul 16, 2026 · Updated 1 time
Summary
This study looks back at medical records of 300 people with metastatic luminal A or luminal B breast cancer who were treated with CDK4/6 inhibitors (Palbociclib, Ribociclib, or Abemaciclib). The goal is to see how long patients lived without their cancer getting worse, and whether the subtype of their cancer affected how well the drugs worked. By comparing real-world outcomes, researchers hope to learn which patients benefit most from these targeted therapies.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- CDK4/6 inhibitors (Palbociclib, Ribociclib, or Abemaciclib)
- What this could lead to
- If successful, this study could help doctors choose the best CDK4/6 inhibitor for each breast cancer subtype, improving treatment personalization.
- What could go wrong
- This is a retrospective review of medical records, not a controlled trial, so results may be influenced by missing data or patient selection bias.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 300 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2021
- Expected to finish
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Apr 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population consists of female patients diagnosed with hormone receptor-positive, HER2-negative (Luminal A or Luminal B) metastatic breast cancer who were managed and treated with CDK4/6 inhibitors at Sohag University Hospital and SCI . Data will be extracted from their existing medical records.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * patients who are more than 18 years old at time of diagnosis and less than 80 years * metastatic breast cancer luminal A and luminal B of either sex Exclusion Criteria: * patients diagnosed with double malignancy * patients with incomplete medical records * patients with organ failure
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Sohag university hospital
Sohag, Egypt
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Other studies related to the condition(s) this trial covers.
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