SHR-A1811 Monotherapy or Sequential THPy as Neoadjuvant Therapy for Stage II-III HER2-Positive Breast Cancer
A Prospective, Multicenter, Exploratory Clinical Study Evaluating the Efficacy and Safety of SHR-A1811 Monotherapy or Sequential THPy as Neoadjuvant Therapy in Stage II-III HER2-positive Breast Cancer
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Tipo de estudio
Tipo de estudio
Inscripción (Estimado)
Inscripción
Fase
Fase
- Fase 2
Contactos y Ubicaciones
Estudio Contacto
Estudio Contacto
- Nombre: Peifen Fu
- Número de teléfono: 0571-87236852
- Correo electrónico: Fupeifen@hotmail.com
Ubicaciones de estudio
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Zhejiang
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Hangzhou, Zhejiang, Porcelana, 310003
- The First Affiliated Hospital, Zhejiang University School of Medicine
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Investigador principal:
- Peifen Fu
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Contacto:
- Minya Yao
- Número de teléfono: 13634111760
- Correo electrónico: yminya@163.com
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Investigador principal:
- Minya Yao
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Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Female aged ≥18 years and ≤75 years.
- Histopathologically confirmed invasive breast cancer with no prior systemic anti-tumor therapy for breast cancer.
- Histopathologically confirmed HER2-positive status in accordance with the 2018 ASCO-CAP HER2 testing guideline criteria: immunohistochemistry (IHC) score of 3+, or IHC 2+ with positive in situ hybridization (ISH) test (ISH amplification ratio ≥2.0); hormone receptor status must be available.
- Stage II-III breast cancer per the 8th edition AJCC Breast Cancer Staging System.
- At least one measurable target lesion according to RECIST Version 1.1.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
Adequate function of major organs as defined below (no blood transfusion, granulocyte-stimulating factors or thrombopoietic agents administered within 2 weeks prior to screening):
- Hematology: absolute neutrophil count (ANC) >1.5×10⁹/L; platelet count (PLT) >75×10⁹/L; hemoglobin (Hb) >90 g/L.
- Serum biochemistry: total bilirubin (TBIL) <1.5×upper limit of normal (ULN); alanine aminotransferase (ALT) and aspartate aminotransferase (AST) <1.5×ULN; alkaline phosphatase <2.5×ULN; blood urea nitrogen (BUN)/urea and creatinine (Cr) <1.5×ULN.
- Echocardiogram: left ventricular ejection fraction (LVEF) ≥55%.
- 12-lead electrocardiogram: Fridericia-corrected QT interval (QTcF) <470 msec.
- For premenopausal women of childbearing potential: serum or urine pregnancy test must be negative within 7 days before treatment initiation; not breastfeeding. All participants must use effective barrier contraception throughout treatment and for 6 months after completion of study treatment.
- Voluntarily provide written informed consent, demonstrate good compliance and willingness to complete scheduled visits and study-related procedures.
Exclusion Criteria:
- Stage IV breast cancer.
- Inflammatory breast cancer.
- Prior anti-tumor therapy or radiotherapy for any malignancy, or concurrent other malignant tumors, except cured carcinoma in situ of cervix, basal cell carcinoma or squamous cell carcinoma.
- Concurrent receipt of anti-tumor therapy in another clinical trial, including but not limited to chemotherapy, endocrine therapy, biotherapy, bone-modifying agent therapy or immune checkpoint inhibitor therapy.
- Major surgery unrelated to breast cancer performed within 4 weeks prior to the first dose of study drug, or participants who have not fully recovered from such surgery.
Severe cardiac disorders, including but not limited to:
- Confirmed history of heart failure or systolic dysfunction (LVEF <50%).
- High-risk uncontrolled arrhythmias, such as atrial tachycardia with resting heart rate >100 bpm, significant ventricular arrhythmia (e.g., ventricular tachycardia), or advanced atrioventricular block (Mobitz type II second-degree or third-degree atrioventricular block).
- Angina requiring anti-anginal medication.
- Electrocardiogram evidence of transmural myocardial infarction.
- Poorly controlled hypertension (systolic blood pressure >180 mmHg and/or diastolic blood pressure >100 mmHg) despite medical treatment.
- Uncontrolled active infection requiring treatment; history of immunodeficiency including positive HIV test, other acquired or congenital immunodeficiency disorders, or history of organ transplantation.
- Known hypersensitivity to any components of study drugs specified in this protocol.
- Pregnant or breastfeeding women; women of childbearing potential with positive baseline pregnancy test; women of childbearing potential unwilling to use effective contraception throughout the study and for 6 months after the last study drug administration.
- Known or suspected interstitial lung disease; moderate to severe pulmonary diseases that may interfere with detection or management of drug-related pulmonary toxicity and severely impair respiratory function within 3 months before 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; any autoimmune, connective tissue or inflammatory diseases involving the lung such as rheumatoid arthritis, Sjogren's syndrome, sarcoidosis; or prior history of pneumonectomy.
- Severe concomitant illnesses or other comorbidities that would interfere with planned treatment, or any other conditions rendering the participant unsuitable for participation in the study as judged by the investigator.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
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Experimental: SHR-A1811 with Response-Guided Therapy
All participants receive an initial 4 cycles of SHR-A1811 (4.8 mg/kg, intravenous infusion every 3 weeks).
After 4 cycles, tumor response is assessed per RECIST 1.1 criteria.
Participants with ≥50% tumor regression continue with another 4 cycles of SHR-A1811, followed by definitive surgery.
Participants with <50% regression switch to 4 cycles of the THPy regimen (docetaxel + trastuzumab + pyrotinib) before surgery.
This is a single-arm, non-randomized, open-label, response-guided treatment strategy.
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SHR-A1811, 4.8 mg/kg, intravenous infusion once every 3 weeks.
All patients receive initial 4 cycles; responders continue additional 4 cycles before surgery.
Combined regimen of docetaxel, trastuzumab, and pyrotinib.
Administered for 4 cycles to patients with insufficient tumor response after the initial 4 cycles of SHR-A1811 prior to definitive surgery.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
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Rate of total pathological complete response (tpCR)
Periodo de tiempo: At the time of definitive surgery (approximately 24 weeks after enrollment)
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At the time of definitive surgery (approximately 24 weeks after enrollment)
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Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
|---|---|
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Rate of breast pathological complete response (bpCR)
Periodo de tiempo: At the time of definitive surgery (approximately 24 weeks after enrollment)
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At the time of definitive surgery (approximately 24 weeks after enrollment)
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Objective Response Rate (ORR)
Periodo de tiempo: After 2 cycles of study treatment (approximately 6 weeks after enrollment)
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After 2 cycles of study treatment (approximately 6 weeks after enrollment)
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Otras medidas de resultado
Otras medidas de resultado
Medida de resultado |
Periodo de tiempo |
|---|---|
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Incidence and severity of Adverse Events (AEs)
Periodo de tiempo: From first study drug administration up to 30 days after the last dose of study treatment
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From first study drug administration up to 30 days after the last dose of study treatment
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Colaboradores e Investigadores
Patrocinador
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Inicio del estudio
Finalización primaria (Estimado)
Finalización primaria
Finalización del estudio (Estimado)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
Otros números de identificación del estudio
- 26-OBU-ZJ-BC-II-020
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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