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Inetetamab Combined With Pyrotinib Plus Oral Vinorelbine for the Treatment of HER2-positive Metastatic Breast Cancer

N

Nanjing Medical University

Status and phase

Enrolling
Phase 2

Conditions

Breast Cancer

Treatments

Drug: Pyrotinib
Drug: Inetetamab
Drug: Oral Vinorelbine Tartrate

Study type

Interventional

Funder types

Other

Identifiers

NCT05823623
2022-SR-494

Details and patient eligibility

About

In this phase 2 single-arm clinical trial, 30 patients with HER2-positive metastatic breast cancer after progression on trastuzumab are enrolled and receive treatment of Inetetamab plus Pyrotinib plus Oral Vinorelbine. The study aimed to access the efficacy and safety of Inetetamab combined with Pyrotinib and Oral Vinorelbine in HER2-positive metastatic breast cancer patients after progression on trastuzumab.

Full description

Trastuzumab is an important agent for the treatment of patients with HER2-positive metastatic breast cancer. However, a considerable number of patients will develop resistance to trastuzumab treatment. Previous studies have shown that multiple mechanisms mediate trastuzumab resistance, such as abnormal extracellular domain of the HER2 receptor, HER3 mutation and activation of bypass signaling pathway. To overcome these resistance mechanisms, the combination of trastuzumab with HER2-targeting tyrosine kinase inhibitor (TKI) is an effective strategy. In this phase 2 single-arm clinical trial, 30 patients with HER2-positive metastatic breast cancer after progression on trastuzumab are enrolled and receive treatment of Inetetamab plus Pyrotinib plus Oral Vinorelbine. The study aimed to access the efficacy and safety of Inetetamab combined with Pyrotinib and Oral Vinorelbine in HER2-positive metastatic breast cancer patients after progression on trastuzumab. The primary end point is Progressive-free Survival (PFS). The secondary end points are Overall Survival (OS), Overall Response Rate (ORR), Clinical Benefit Rate (CBR) and safety.

Enrollment

30 estimated patients

Sex

Female

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Female, Aged ≥ 18 years.
  2. Metastatic breast cancer confirmed by pathology or imaging.
  3. Pathological diagnosis of HER2 positive (definition: immunohistochemical (IHC) 3+, or IHC 2+ with in situ hybridization (ISH) testing of amplification.
  4. Previously received trastuzumab treatment.
  5. At least one Measurable target lesion according to RECIST 1.1.
  6. Eastern Cooperative Oncology Group (ECOG) score 0- 2.
  7. Sufficient organ function: Neutrophil count (ANC) ≥ 1.5 × 10 ^ 9 / L, Platelet count (PLT) ≥ 100 × 10 ^ 9 / L, hemoglobin (Hb) ≥90 g/L,total bilirubin (TBIL) ≤ 1.5 × upper limit of normal value (ULN), alanine aminotransferase (ALT / AST) ≤ 2.5 × ULN (liver metastasis patients ≤ 5×ULN), serum creatinine ≤ 1.5 × ULN or creatinine clearance rate (CCR) ≥ 60 ml/min, Left ventricular ejection fraction (LVEF) ≥50%.

Exclusion criteria

  1. Allergic to the ingredients of the study drug.
  2. Symptomatic brain or meningeal metastasis.
  3. Gastrointestinal dysfunction or gastrointestinal diseases (including active ulcers).
  4. LVEF <50%; clinical manifestations of patients with obvious arrhythmia, myocardial ischemia, severe atrioventricular block, cardiac insufficiency, and severe valvular disease.
  5. Any other medical, social or psychological conditions which are inappropriate to participate in this trial.
  6. Pregnant or lactating women, women of childbearing age who refused to take effective contraceptive measures during the study period.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Inetetamab combined with Pyrotinib plus Oral Vinorelbine
Experimental group
Description:
Inetetamab: 8mg/kg for the first dose, 6mg/kg for the following doses, intravenous, every 3 weeks for one cycle. Pyrotinib: 400mg, oral, every day. Vinorelbine: 60mg/m2, oral, every week.
Treatment:
Drug: Oral Vinorelbine Tartrate
Drug: Pyrotinib
Drug: Inetetamab

Trial contacts and locations

1

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Central trial contact

Xiang Huang

Data sourced from clinicaltrials.gov

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