Actively Recruiting

All Genders
NCT06693037

Adjuvant Therapy Choice for Non-pCR HER2 Positive Early Breast Cancer After Neoadjuvant Therapy

Led by Shu Wang · Updated on 2024-11-20

2092

Participants Needed

1

Research Sites

678 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Chemotherapy combined with trastuzumab and patuzumab is the standard neoadjuvant therapy for HER2 positive breast cancer patients. The survival rate of patients with pathological complete response (PCR) after neoadjuvant therapy was significantly better than that of patients with tumor residue, that is, non-PCR. Therefore, studies have confirmed that adjuvant therapy for patients with non-PCR after neoadjuvant chemotherapy can further improve the prognosis and survival of this population. However, the results of previous studies are based on trastuzumab target therapy in neoadjuvant therapy. Therefore, there are different recommendations for the current guidelines of adjuvant therapy after trastuzumab combined pertuzumab target neoadjuvant therapy. Patients with HER2 positive breast cancer who received trastuzumab and patuzumab based neoadjuvant therapy had invasive residual cancer in postoperative pathology. The effect of postoperative adjuvant therapy with trastuzumab and patuzumab or replacement of T-DM1 on survival.

CONDITIONS

Official Title

Adjuvant Therapy Choice for Non-pCR HER2 Positive Early Breast Cancer After Neoadjuvant Therapy

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with HER2-positive breast cancer by biopsy at Peking University People's Hospital
  • Clinical stage before treatment is T1-T4, N0-N3, M0
  • Received treatment and surgery at the hospital with hospitalization records
  • Completed at least 4 cycles of trastuzumab and pertuzumab combined chemotherapy as neoadjuvant therapy
  • Postoperative pathology shows residual invasive breast cancer in breast or metastatic tumor in axillary lymph nodes
  • Signed and agreed to participate in the PKUPH breast disease cohort study
Not Eligible

You will not qualify if you...

  • Missing clinical or pathological data such as imaging or pathology reports
  • Having metastatic breast cancer or bilateral breast cancer
  • Did not undergo radical surgery
  • Received any neoadjuvant therapy regimens other than the established trastuzumab and pertuzumab regimen

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Peking University People's Hospital

Beijing, Beijing Municipality, China, 100044

Actively Recruiting

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Research Team

Y

yuan peng, doctor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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