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Neoadjuvant pyrotinib in patients with HER2-positive breast cancer:a multicentre, retrospective real-world study

Neoadjuvant pyrotinib in patients with HER2-positive breast cancer:a multicentre, retrospective real-world study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100048895
Enrollment
Unknown
Registered
2021-07-19
Start date
2021-07-19
Completion date
Unknown
Last updated
2022-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast cancer

Interventions

Sponsors

The fist hospital of china medical university
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years; 2. Histopathological examination confirmed invasive breast cancer with positive HER2; 3. The tumor stage is early or locally advanced; 4. To receive a regimen containing pyrotinib as neoadjuvant therapy; 5. If targeted drugs are changed during neoadjuvant therapy, it is required that the last targeted drugs used preoperatively include pyrotinib; 6. Surgery has been performed and pathological examination results are available; 7. Have traceable medical history.

Exclusion criteria

Exclusion criteria: 1. Prior anti-tumor therapy or radiation therapy for any malignancy, not including cured carcinoma in situ of the cervix, basal cell carcinoma, or squamous cell carcinoma; 2. Patients who received other TKI anti-HER2 therapies during neoadjuvant therapy; 3. Patients enrolled in other studies; 4. The Investigator considers the patient unsuitable for participation in any other condition of the study.

Design outcomes

Primary

MeasureTime frame
pathological complete remission;

Secondary

MeasureTime frame
total pathological complete remission;objective remission rate;safety;

Countries

China

Contacts

Public ContactJin Feng

The fist hospital of china medical university

jinfeng66cn@hotmail.com+86 13898890665

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026