HER2+ Metastatic Breast Cancer in Kazakhstan (observational)
Official title: A Multicenter Observational Retrospective Study of Therapeutic Approaches and Clinical Outcomes in Real Clinical Practice in Kazakhstan Patients With Human Epidermal Growth Factor Receptor 2 (HER2)-Positive Metastatic Breast Cancer
Run by AstraZeneca · NCT07593196 · Data updated 2026-11-12
This study tests how patients with HER2-positive metastatic breast cancer who are receiving anti-HER2 therapy fare across several Kazakh centers.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 99 Years |
| Sex | All |
| Enrollment | 240 (estimated) |
| Sponsor | AstraZeneca Industry-sponsored |
| Drugs / interventions | trastuzumab |
| Locations | 12 sites (Oral, Kazakhstan and 11 other locations) |
| Status | Recruiting |
| Started | June 12, 2026 |
| Main results expected | December 31, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | October 8, 2026 |
| Trial ID | NCT07593196 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adult patients (age 18+) with HER2-positive metastatic breast cancer who are on or started anti-HER2 therapy (excluding trastuzumab deruxtecan) and have sufficient follow-up data.
✕Probably not a fit
Patients who do not have adequate follow-up data or who are receiving trastuzumab deruxtecan may have limited benefit from the findings.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study plans to enroll about 240 adults with HER2-positive metastatic breast cancer treated with anti-HER2 therapy across 12 centers in different regions of Kazakhstan. Participants will be enrolled in order of diagnosis date within a defined timeframe, and retrospective follow-up will extend at least 12 months after the latest diagnosis to capture outcomes. Data collection focuses on real-world treatment patterns and outcomes without a specified intervention. Key eligibility requires documented HER2-positive metastatic disease diagnosed between 2022 and 2023 and at least 24 months of follow-up data unless death, relocation, or early discontinuation occurs. The study is sponsored by AstraZeneca and involves sites in Oral, Aktobe, and Almaty.
Why it matters
Potential benefit: If successful, the study could provide real-world insights into treatment patterns and outcomes for HER2-positive mBC in Kazakhstan.
How similar studies have gone: Similar observational studies have shown value in real-world treatment patterns for HER2-positive breast cancer, though this particular Kazakhstani cohort is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with HER2-positive mBC who are receiving or have started any anti-HER2 therapy (except for trastuzumab deruxtecan) at the time of inclusion * The diagnosis of mBC was established between the 1st January 2022 to 31st December 2023 * Patients with the availability of at least 24 months of follow-up data (from the date of mBC diagnosis) in the medical records at the participating site, unless patient died/moved or refused the therapy within the first 24 months of diagnosis * Age ≥18 years at the time of inclusion Exclusion Criteria: * Presence of other malignancies within the period from mBC diagnosis until the timepoint of data collection * Patients received trastuzumab deruxtecan * The participation in any interventional trial within period since diagnosis until the end of study
Where it's running
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Research Site
Oral, Kazakhstan, Kazakhstan Recruiting -
Research Site
Almaty, Kazakhstan Recruiting -
Research Site
Almaty, Kazakhstan Recruiting -
Research Site
Astana, Kazakhstan Recruiting -
Research Site
Astana, Kazakhstan Recruiting -
Research Site
Karaganda, Kazakhstan Recruiting
Show 6 more locations
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Research Site
Petropavl, Kazakhstan Recruiting -
Research Site
Semey, Kazakhstan Recruiting -
Research Site
Shymkent, Kazakhstan Recruiting -
Research Site
Taraz, Kazakhstan Recruiting -
Research Site
Aktobe, Kazakhstan Not yet recruiting -
Research Site
Shymkent, Kazakhstan Not yet recruiting
Study contacts
- Study coordinator: AstraZeneca Clinical Study Information Center
- Email: information.center@astrazeneca.com
- Phone: 1-877-240-9479
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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PRT13722 in advanced HR+/HER2- breast cancer
This early study tests PRT13722, by itself and with standard therapies, to see if it is safe and has any signs of activity in adults with HR+/HER2- breast cancer who have progressed on prior treatments.
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Personalized treatment after endocrine therapy failure in metastatic breast cancer
The study tests whether using a patient’s fresh tumor sample to try different drugs outside the body can help pick the next therapy for hormone receptor-positive, HER2-negative metastatic breast cancer that progressed on endocrine therapy.
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SSGJ-612 plus a HER2-targeted ADC in HR-positive, HER2-low metastatic breast cancer
This phase II study tests whether adding SSGJ-612 to a HER2-targeted antibody-drug conjugate helps people with HR-positive, HER2-low or ultralow metastatic breast cancer.
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SMP-656 in HER2-positive advanced breast cancer after ADC therapy
This trial tests whether SMP-656 given by IV every 3 weeks can help people with HER2-positive locally advanced or metastatic breast cancer who progressed after a HER2-targeted antibody-drug conjugate.
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Entinostat with Pyrotinib and Endocrine Therapy in HER2-positive, HR-positive Advanced Breast Cancer after Trastuzumab Failure
This study tests whether adding entinostat to pyrotinib and hormone therapy is safe and helps patients with advanced HR+/HER2+ breast cancer who progressed after trastuzumab.
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T-DXd–based therapy followed by targeted HER2 blockade and endocrine therapy in first-line HER2+ / HR+ metastatic breast cancer
This trial tests a sequence of therapies starting with T-DXd plus pertuzumab, then a maintenance phase with dual HER2 blockade, endocrine therapy, and CDK4/6 inhibitor, with a retreatment option of T-DXd if disease progresses.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.