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RecruitingNCT07358182Updated Jan 22, 2026

Efficacy and Safety of Trastuzumab-rezetecan in HER2-Expressing Breast Cancer

An observational study in Trastuzumab-rezetecan, HER2-low Breast Cancer and HER2-positive Breast Cancer, sponsored by Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University. Recruiting at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-01-22.

Sponsored by Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University · Observational

From the registry’s dates

  • Started Jun 2025; still recruiting 1 year 4 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
300
Ages
18 Years and older
Sex
All
01

Study summary

This study is a multicenter, observational, real-world investigation. The research plans to enroll 300 HER2-positive and HER2-low breast cancer patients who meet the inclusion criteria. All patients included in the analysis are currently receiving or are scheduled to receive a treatment regimen containing Trastuzumab-rezetecan. There are no restrictions on the treatment regimen, which is entirely based on the clinician's choice. The study aims to evaluate the efficacy and safety of the treatment regimen containing Trastuzumab-rezetecan.

After completing screening examinations and assessments, eligible patients will enter the study treatment phase. They will receive the treatment regimen containing Trastuzumab-rezetecan and undergo follow-up visits according to the protocol. During the study treatment period, patients will undergo imaging and safety assessments as per clinical routine, with the investigator's assessment serving as the final result. Upon treatment completion or study withdrawal, corresponding safety examinations and imaging assessment data will be collected. For neoadjuvant patients, pathological complete response (pCR) will be assessed post-surgery by pathologists at the participating centers.

02

Conditions studied

  • Trastuzumab-rezetecan
  • HER2-low Breast Cancer
  • HER2-positive Breast Cancer
03

In context

Lead sponsor

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University is the lead sponsor of 466 studies on the registry; 271 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

HER2-positive and HER2-low breast cancer patients, including all those analyzed who are currently receiving or plan to receive a treatment regimen containing Trastuzumab-rezetecan.

Inclusion criteria

  1. Age ≥ 18 years, with pathologically confirmed HER2-positive or HER2-low-expressing breast cancer: HER2-positive is defined as IHC 3+ or IHC 2+ with a positive ISH result; HER2-low-expressing is defined as IHC 1+ or IHC 2+ with a negative ISH result for HER2 amplification; hormone receptor status must be clearly documented.
  2. Planned to receive treatment with Trastuzumab-rezetecan for Injection in the neoadjuvant, adjuvant, or advanced/metastatic setting; patients with advanced/metastatic disease must have progressed after at least one prior line of systemic therapy.
  3. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-2.
  4. Women of childbearing potential must have a negative serum pregnancy test within 28 days prior to enrollment, and both male and female patients must be willing to use a highly effective, medically approved method of contraception during the study and for 1 year after the last dose of the study drug.
  5. Non-pregnant and non-lactating female patients.
  6. Not concurrently participating in any other ongoing clinical studies. The patient or their legal representative has provided informed consent by signing the informed consent form and is willing and able to comply with scheduled visits, the study treatment plan, laboratory tests, and other trial procedures.

Exclusion criteria

Exclusion Criteria:

  1. Any evidence of severe or uncontrolled systemic disease, including uncontrolled hypertension, active bleeding disorders, active infections (such as hepatitis B, hepatitis C, and human immunodeficiency virus), or severely impaired bone marrow reserve or organ function (including hepatic and renal impairment), which, in the investigator's opinion, would significantly alter the risk-benefit balance.
  2. At the initiation of treatment with Trastuzumab-rezetecan for Injection, the patient has not recovered from any prior treatment-related toxicity of CTCAE grade >3.
  3. Known history of hypersensitivity to Trastuzumab-rezetecan for Injection, its excipients, or drugs with similar chemical structures or classes as Trastuzumab-rezetecan.
  4. Patients deemed unsuitable for enrollment by the investigator.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
300 participants (estimated)
Patient registry
No

Groups and cohorts

  • Trastuzumab-rezetecan Treatment Group

    Drug: Trastuzumab-rezetecan Treatment Group

Interventions

  • DrugTrastuzumab-rezetecan Treatment Group

    Trastuzumab-rezetecan: 4.8 mg/kg (for HER2-positive) or 6.4 mg/kg (for HER2-low) per treatment cycle of 21 days. The dosage is to be adjusted at the discretion of the investigator based on the actual clinical situation. All patients will receive treatment with a regimen containing Trastuzumab-rezetecan as determined by the investigator. The regimens for other concomitant medications will be selected by the treating physician based on the patient's individual circumstances.

06

What researchers measure

Primary outcomes

  1. Adverse events (AEs)

    Assessed per NCI-CTCAE v5.0 criteria

    Time frame: From the signing of the informed consent form until 30 days after the last dose

Secondary outcomes

  1. Pathological Complete Response(pCR)

    No residual invasive cancer is found upon evaluation of the excised breast tissue and regional lymph nodes

    Time frame: Estimated 7 years

  2. Invasive disease free survival(iDFS)

    Time from randomization to the first occurrence of ipsilateral local/regional invasive recurrence, distant metastasis, contralateral invasive breast cancer, or death from any cause.

    Time frame: Estimated 7 years

  3. Progression-free survival (PFS)

    The date of randomization to the first documented disease progression (per RECIST 1.1) or death due to any cause, whichever occurred first

    Time frame: Estimated 7 years

  4. Objective Response Rate (ORR)

    The percentage of patients with ≥30% tumor shrinkage, as evaluated by investigators per RECIST 1.1 criteria

    Time frame: Estimated 7 years

  5. Clinical Benefit Rate (CBR)

    Sum of complete response \[CR\], partial response \[PR\], and SD lasting ≥24 weeks), as assessed by investigators according to RECIST 1.1 criteria

    Time frame: Estimated 7 years

  6. Overall Survival (OS)

    The duration from randomization to death event

    Time frame: Estimated 7 years

07

Study locations

1 of 1 sites recruiting
  • Breast Tumor Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University
    Guangzhou, Guangdong, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07358182
Lead sponsor
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Responsible party
Sponsor
First posted
Jan 22, 2026
Start date
Jun 1, 2025
Primary completion
Jun 30, 2029 (estimated)
Completion
Jun 30, 2031 (estimated)
Last update
Jan 22, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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