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Efficacy and Safety of Trastuzumab Rezetecan or Trastuzumab Deruxtecan in Advanced Breast Cancer

A Comparison of the Efficacy and Safety of Trastuzumab Rezetecan(SHR-A1811) Versus Trastuzumab Deruxtecan(DS-8201) in Patients With HER2-Positive Metastatic Breast Cancer Previously Treated With Trastuzumab

This study is a prospective, open-label, multicenter, randomized, parallel Phase II clinical trial. This study aims to investigate the efficacy and safety of trastuzumab rezetecan or trastuzumab deruxtecan in HER2 positive advanced/metastastic breast cancer

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Estimado)

100

Estágio

  • Fase 2

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

  • Nome: herui Yao, PhD, MD
  • Número de telefone: +86 13500018020
  • E-mail: yaoherui@163.com

Locais de estudo

    • Guangdong
      • Guangzhou, Guangdong, China
        • Sun Yat-sen Memorial Hospital
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • Female patients aged ≥18 and ≤75 years.
  • Histologically or cytologically confirmed HER2-positive (IHC 3+ and/or ISH positive) unresectable or metastatic breast cancer.
  • Prior treatment with trastuzumab and a taxane in the recurrent or metastatic setting. Or recurrence during or within 12 months (disease-free interval, DFI) after completing neoadjuvant/adjuvant chemotherapy and/or anti-HER2 targeted therapy.
  • Documented radiological disease progression (during or after the most recent prior therapy).
  • ECOG Performance Status of 0 or 1.
  • At least one measurable lesion according to RECIST v1.1 criteria.
  • Adequate organ function meeting the following criteria (without the use of any blood components, cytokines, or growth factors for correction within 14 days prior to the first dose):

Absolute neutrophil count (ANC) ≥1.5 × 10⁹/L; Platelet count (PLT) ≥100 × 10⁹/L; Hemoglobin (Hb) ≥90 g/L (9.0 g/dL); Albumin ≥3.0 g/dL;Total bilirubin ≤1.5 × ULN; Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5 × ULN (≤5.0 × ULN for patients with liver metastases); Serum creatinine ≤1.5 × ULN OR creatinine clearance ≥60 mL/min (calculated using the Cockcroft-Gault formula); QTcF interval ≤470 ms; Left ventricular ejection fraction (LVEF) ≥50% as measured by echocardiography (ECHO) or multigated acquisition scan (MUGA)

  • Female subjects of childbearing potential must have a negative pregnancy test at screening and must agree to use highly effective contraception methods from the signing of the informed consent form until 7 months after the last dose of the investigational product.
  • Willing and able to provide written informed consent, with good compliance, and willing to cooperate with follow-up visits and study-related procedures.

Exclusion Criteria:

  • Patients with known untreated spinal cord compression or active central nervous system (CNS) metastases, except for those who have been treated and have remained stable for at least 1 month and have discontinued corticosteroids for >2 weeks.
  • History of other malignancies within the past 5 years, excluding cured basal cell carcinoma of the skin and carcinoma in situ of the cervix.
  • Uncontrolled third-space fluid accumulation (e.g., massive ascites, pleural effusion, pericardial effusion) that cannot be managed by drainage or other methods.
  • Having undergone major cancer-related surgery, radiotherapy, chemotherapy, immunotherapy, molecular targeted therapy, biotherapy, or other clinical investigational therapy within 4 weeks prior to the first dose.
  • Prior treatment with an antibody-drug conjugate containing an exatecan derivative (a topoisomerase I inhibitor).
  • Use of immunosuppressants or systemic corticosteroids for immunosuppressive purposes (at doses >10 mg/day prednisone or equivalent) within 2 weeks prior to the first dose, excluding topical, nasal spray, or inhaled corticosteroids.
  • Presence of any active autoimmune disease or a history of autoimmune disease that may potentially recur.
  • History of immunodeficiency, including a positive HIV test, other acquired or congenital immunodeficiency diseases, or a history of organ transplantation.
  • Patients with known or suspected interstitial lung disease (ILD); or presence of other moderate-to-severe pulmonary diseases that may significantly impair respiratory function or interfere with the detection or management of drug-related pulmonary toxicity within 3 months prior to the first dose, including but not limited to idiopathic pulmonary fibrosis, organizing pneumonia/bronchiolitis obliterans, pulmonary embolism, severe asthma, severe chronic obstructive pulmonary disease (COPD), obstructive/restrictive lung disease, etc.; and any autoimmune, connective tissue, or inflammatory disorders involving the lungs, such as rheumatoid arthritis, Sjögren's syndrome, sarcoidosis, etc.; or history of pneumonectomy. Patients who experienced ≥Grade 3 ILD during prior treatment with immune checkpoint inhibitors are excluded.
  • Presence of active hepatitis B (HBsAg positive and HBV DNA ≥500 IU/mL), hepatitis C (anti-HCV positive and HCV RNA above the upper limit of normal), or liver cirrhosis; or severe infections requiring systemic antibiotic, antiviral, or antifungal therapy.
  • Toxicities from prior anti-tumor therapy that have not recovered to ≤ Grade 1 (according to NCI-CTCAE v6.0).
  • Known hypersensitivity to any of the study drugs or their excipients.
  • Any other severe physical or mental illness or abnormal laboratory finding that, in the investigator's judgment, may increase the risk associated with study participation, interfere with the study results, or make the patient unsuitable for participation in this study.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: SHR-A1811
SHR-A1811 4.8mg/kg iv q3w
Outros nomes:
  • SHR-A1811
  • T-dxh
  • Trastuzumab rezetecan
Comparador Ativo: T-DXd
T-DXd 5.4mg/kg iv q3w
Outros nomes:
  • T-DXd
  • DS-8201
  • Trastuzumabe deruxtecano

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Progression Free Survival(PFS)
Prazo: From the date of randomization to the earliest date of the first objective documentation of radiographic disease progression or death due to any cause, up to approximately 3 years
Time from the date of randomization until the date of first documented radiological disease progression (PD) or death from any cause, whichever occurs first. If a subject did not experience PD or death by the data cutoff date, or had received other anti-tumor therapy, censoring occurred at the date of the last efficacy assessment prior to the cutoff date or the start date of other anti-tumor therapy, whichever was earlier.
From the date of randomization to the earliest date of the first objective documentation of radiographic disease progression or death due to any cause, up to approximately 3 years

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Eventos Adversos Emergentes do Tratamento (EAET) e Eventos Adversos Graves Emergentes do Tratamento (EAGET)
Prazo: Desde a primeira dose do medicamento do estudo (Dia 1) até aproximadamente 3 anos
Desde a primeira dose do medicamento do estudo (Dia 1) até aproximadamente 3 anos
Objective response rate (ORR)
Prazo: From screening and every 6 weeks up to withdrawal of subject consent, progressive disease (PD), or unacceptable toxicity, up to approximately 3 years
The percentage of subjects in the analysis set whose best overall response (BOR) was a complete response (CR) or partial response (PR) from the start of the study treatment until the subject discontinued the study due to disease progression. It is recommended to use the Response Evaluation Criteria in Solid Tumors (RECIST 1.1) to evaluate the objective tumor response. Subjects must have measurable tumor lesions at baseline, and the assessment of efficacy is recommended to be categorized according to RECIST 1.1 criteria into complete response (CR), partial response (PR), stable disease (SD), and progressive disease (PD).
From screening and every 6 weeks up to withdrawal of subject consent, progressive disease (PD), or unacceptable toxicity, up to approximately 3 years
Disease control rate(DCR)
Prazo: From screening and every 6 weeks up to withdrawal of subject consent, progressive disease (PD), or unacceptable toxicity, up to approximately 3 years
The percentage of subjects in the analysis set whose best overall response (BOR) was complete response (CR), partial response (PR), or stable disease (SD) from the start of the study treatment regimen until the subject discontinued the study due to disease progression. It is recommended to use the Response Evaluation Criteria in Solid Tumors (RECIST 1.1) to assess the objective tumor response. Subjects must have measurable tumor lesions at baseline, and the efficacy assessment is recommended to be categorized according to RECIST 1.1 criteria as complete response (CR), partial response (PR), stable disease (SD), and progressive disease (PD).
From screening and every 6 weeks up to withdrawal of subject consent, progressive disease (PD), or unacceptable toxicity, up to approximately 3 years
Duration of Response(DOR)
Prazo: From the date of the first documented objective response (CR or PR) to the first documented disease progression or death, whichever occurs first, up to approximately 3 years
defined as the time from the date of first documented response (complete response, CR, or partial response, PR, whichever occurs first) to the date of disease progression or death, whichever occurs earlier. Response is assessed using the Response Evaluation Criteria in Solid Tumors (RECIST 1.1).
From the date of the first documented objective response (CR or PR) to the first documented disease progression or death, whichever occurs first, up to approximately 3 years
Overall survival (OS)
Prazo: From the date of randomization up to the date of death due to any cause, up to approximately 3 years
Defined as the time from the date of enrollment to the date of death from any cause. For subjects who were alive at the last follow-up, their OS data are censored at the date of the last follow-up. For subjects who were lost to follow-up, their OS data are censored at the date of the last documented evidence of survival prior to being lost. Censored OS is defined as the time from enrollment to censoring.
From the date of randomization up to the date of death due to any cause, up to approximately 3 years

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de junho de 2026

Conclusão Primária (Estimado)

1 de junho de 2031

Conclusão do estudo (Estimado)

1 de dezembro de 2031

Datas de inscrição no estudo

Enviado pela primeira vez

1 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

1 de junho de 2026

Primeira postagem (Real)

5 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

5 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

1 de junho de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • MA-BC-II-137

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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