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- Ensayo clínico NCT07752550
Retlirafusp Alfa Combined With Chemotherapy or Fuzuloparib for Triple-Negative Breast Cancer
Retlirafusp Alfa Combined With Chemotherapy or Fuzuloparib for Triple-Negative Breast Cancer: An Exploratory Clinical Study
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Tong Liu, M.D.
- Número de teléfono: +8615945953777
- Correo electrónico: liutong@hrbmu.edu.cn
Ubicaciones de estudio
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Heilongjiang
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Harbin, Heilongjiang, Porcelana, 150081
- Harbin Medical University Cancer Hospital
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Age ≥18 years, female;
- Histopathologically confirmed recurrent or metastatic triple-negative breast cancer, defined as ER-negative (IHC ER-positive percentage <1%), PR-negative (IHC PR-positive percentage <1%), and HER2-negative (IHC -/+ or IHC ++ but FISH/CISH -);
- At least one measurable lesion per RECIST version 1.1 criteria;
Advanced cohort:
Metastatic or unresectable locally advanced TNBC (no prior systemic therapy or completed neoadjuvant/adjuvant therapy ≥12 months); PD-L1 positive with a Combined Positive Score (CPS) ≥1;
Neoadjuvant cohort:
Clinical stage II (T2N0-1M0/T3N0M0) or III (T2N2-3M0/T3N1-3M0) previously untreated breast cancer patients;
- Life expectancy ≥3 months;
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-1;
- Available tissue sample for testing, and gBRCA1/2 mutation status must be determined prior to treatment;
Adequate major organ function meeting the following criteria (no blood transfusion or use of granulocyte colony-stimulating factor or thrombopoietin within 2 weeks prior to screening):
Hematologic: Absolute neutrophil count (ANC) ≥1.5×10⁹/L; platelet count (PLT) ≥90×10⁹/L; hemoglobin (Hb) ≥90 g/L; Biochemical: Total bilirubin (TBIL) ≤1.5× upper limit of normal (ULN); ALT and AST ≤1.5× ULN (≤3× ULN for patients with liver metastases); alkaline phosphatase ≤2.5× ULN; BUN and creatinine ≤1.5× ULN with creatinine clearance ≥50 mL/min (calculated by Cockcroft-Gault formula); Thyroid-stimulating hormone (TSH) ≤ULN (if abnormal, T3 and T4 levels should also be assessed; patients with normal T3 and T4 levels may be enrolled); Echocardiography: Left ventricular ejection fraction (LVEF) ≥50%; 18-lead electrocardiogram: Fridericia-corrected QT interval (QTcF) <480 ms for females;
- Women of childbearing potential must have a negative serum or urine pregnancy test within 7 days prior to enrollment and agree to use adequate contraception during the study period and for at least 4 months after the last dose of study drug;
- Willing to participate, capable of providing signed informed consent, and compliant with study procedures.
Exclusion Criteria:
- Concurrently receiving anti-tumor therapy in another clinical trial;
- Received other anti-tumor therapy within 4 weeks prior to the first dose of study drug;
- Prior treatment with tumor immunotherapy (including but not limited to PD-1, PD-L1, CTLA-4 inhibitors, etc.) or TGF-β inhibitors;
- Prior treatment with PARP inhibitors (except for patients who completed PARP inhibitor therapy for ovarian cancer ≥5 years ago with no recurrence or metastasis);
- Untreated active brain metastases or leptomeningeal metastases;
- Underwent major surgery unrelated to breast cancer within 4 weeks prior to enrollment, or have not fully recovered from such surgery;
- Presence of any active autoimmune disease or history of autoimmune disease (including but not limited to autoimmune hepatitis, interstitial pneumonia, uveitis, enteritis, hepatitis, hypophysitis, vasculitis, nephritis, hyperthyroidism, hypothyroidism); patients with vitiligo or childhood asthma that has completely resolved and does not require any intervention in adulthood may be included; patients with asthma requiring bronchodilator therapy for medical intervention are excluded;
- Severe cardiac disease or conditions, including but not limited to: documented history of heart failure or systolic dysfunction (LVEF <50%); uncontrolled high-risk arrhythmias, such as atrial tachycardia, resting heart rate >100 bpm, significant ventricular arrhythmias (e.g., ventricular tachycardia), or high-grade atrioventricular block (i.e., Mobitz II second-degree or third-degree atrioventricular block); angina requiring anti-anginal medication; clinically significant valvular heart disease; ECG showing transmural myocardial infarction; poorly controlled hypertension (systolic blood pressure >180 mmHg and/or diastolic blood pressure >100 mmHg);
- Congenital or acquired immunodeficiency (e.g., HIV-infected patients);
- Received live vaccine within 4 weeks prior to study drug administration or likely to receive such vaccine during the study period;
- Known hypersensitivity to any component of the study drugs in this protocol;
- Severe concomitant disease or other comorbidities that may interfere with the planned treatment, or any other condition that, in the investigator's opinion, makes the patient unsuitable for participation in this study.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Advanced cohort: gBRCA1/2 wild-type
Retlirafusp alfa + nab-paclitaxel
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Retlirafusp alfa+Nab-paclitaxel
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Experimental: Advanced cohort: gBRCA1/2 pathogenic or likely pathogenic mutation
Retlirafusp alfa + fluzoparib
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Retlirafusp alfa+Fluzoparib
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Experimental: Early neoadjuvant cohort: gBRCA1/2 wild-type
Retlirafusp alfa+TP-AC
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Retlirafusp alfa+TP-AC
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Experimental: Early neoadjuvant cohort: gBRCA1/2 pathogenic or likely pathogenic mutation
Retlirafusp alfa+ Fluzoparib
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Retlirafusp alfa+Fluzoparib
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Late-Stage Cohort-Objective Response Rate
Periodo de tiempo: Assessed every 6 weeks (every 2 cycles) during treatment until disease progression, death, or loss to follow-up. Analysis cutoff at 6 months.
|
Proportion of patients with best overall response of complete response (CR) or partial response (PR) from treatment initiation to disease progression.
|
Assessed every 6 weeks (every 2 cycles) during treatment until disease progression, death, or loss to follow-up. Analysis cutoff at 6 months.
|
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Neoadjuvant Cohort-tpCR (ypT0/is ypN0)
Periodo de tiempo: Surgery performed 2-6 weeks after completing 8 cycles (≈24 weeks) of neoadjuvant therapy; pathological assessment post-surgery. Analysis cutoff at 6 months.
|
Pathologic complete response with no residual invasive carcinoma in breast and ipsilateral lymph nodes after neoadjuvant therapy and surgery.
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Surgery performed 2-6 weeks after completing 8 cycles (≈24 weeks) of neoadjuvant therapy; pathological assessment post-surgery. Analysis cutoff at 6 months.
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Late-Stage Cohort-Disease Control Rate
Periodo de tiempo: Assessed every 6 weeks (every 2 cycles) during treatment until disease progression, death, or loss to follow-up. Analysis cutoff at 6 months.
|
Proportion of patients with best overall response of CR, PR, or stable disease (SD) from treatment initiation to disease progression.
|
Assessed every 6 weeks (every 2 cycles) during treatment until disease progression, death, or loss to follow-up. Analysis cutoff at 6 months.
|
|
Late-Stage Cohort-Clinical Benefit Rate
Periodo de tiempo: Assessed until disease progression, death, or loss to follow-up. Analysis cutoff at 6 months.
|
Proportion of patients with confirmed CR, PR, or SD lasting ≥24 weeks.
|
Assessed until disease progression, death, or loss to follow-up. Analysis cutoff at 6 months.
|
|
Late-Stage Cohort-Progression-Free Survival
Periodo de tiempo: Assessed every 3 months during treatment and follow-up until disease progression, death, or start of subsequent anticancer therapy. Analysis cutoff at 36 months.
|
Time from treatment initiation to first radiographic disease progression or death from any cause.
|
Assessed every 3 months during treatment and follow-up until disease progression, death, or start of subsequent anticancer therapy. Analysis cutoff at 36 months.
|
|
Late-Stage Cohort-Overall Survival
Periodo de tiempo: Follow-up every 3 months via clinic visit or telephone call after treatment completion until death or study end. Analysis cutoff at 36 months.
|
Time from treatment initiation to death from any cause.
|
Follow-up every 3 months via clinic visit or telephone call after treatment completion until death or study end. Analysis cutoff at 36 months.
|
|
Neoadjuvant Cohort-bpCR (ypT0/is)
Periodo de tiempo: Surgery performed 2-6 weeks after completing 8 cycles (≈24 weeks) of neoadjuvant therapy; pathological assessment post-surgery. Analysis cutoff at 6 months.
|
Pathologic complete response with no residual invasive carcinoma in breast (lymph node status disregarded) after neoadjuvant therapy and surgery.
|
Surgery performed 2-6 weeks after completing 8 cycles (≈24 weeks) of neoadjuvant therapy; pathological assessment post-surgery. Analysis cutoff at 6 months.
|
|
Neoadjuvant Cohort-Objective Response Rate
Periodo de tiempo: Assessed every 6 weeks (every 2 cycles) during neoadjuvant therapy until treatment completion. Analysis cutoff at 6 months.
|
Proportion of patients with best overall response of CR or PR during neoadjuvant therapy.
|
Assessed every 6 weeks (every 2 cycles) during neoadjuvant therapy until treatment completion. Analysis cutoff at 6 months.
|
|
Neoadjuvant Cohort-Event-Free Survival
Periodo de tiempo: Follow-up every 3 months from treatment start until event or study end. Analysis cutoff at 36 months.
|
Time from treatment initiation to first occurrence of preoperative disease progression, postoperative recurrence, or death from any cause.
|
Follow-up every 3 months from treatment start until event or study end. Analysis cutoff at 36 months.
|
|
Neoadjuvant Cohort-Disease-Free Survival
Periodo de tiempo: Follow-up every 3 months from surgery until recurrence, death, or study end. Analysis cutoff at 36 months.
|
Time from surgery to first postoperative recurrence or death from any cause.
|
Follow-up every 3 months from surgery until recurrence, death, or study end. Analysis cutoff at 36 months.
|
|
Neoadjuvant Cohort-Distant Disease-Free Survival
Periodo de tiempo: Follow-up every 3 months from surgery until distant metastasis, death, or study end. Analysis cutoff at 36 months.
|
Time from surgery to first distant metastasis or death from any cause.
|
Follow-up every 3 months from surgery until distant metastasis, death, or study end. Analysis cutoff at 36 months.
|
|
Adverse Event (AE) Incidence
Periodo de tiempo: Recorded from informed consent signing through 30 days after last dose (SAEs and immune-related AEs through 90 days after last dose); maximum follow-up of 36 months.
|
Incidence, severity, and drug-relatedness of AEs and SAEs, graded per NCI-CTCAE v6.0.
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Recorded from informed consent signing through 30 days after last dose (SAEs and immune-related AEs through 90 days after last dose); maximum follow-up of 36 months.
|
|
Biomarker Exploration
Periodo de tiempo: Blood samples collected at baseline, Cycle 5 Day 1, and Cycle 8 Day 1 (21-day cycle); tumor tissue collected at baseline from archived FFPE blocks or fresh biopsy. Analysis cutoff at 6 months.
|
Collection of tumor tissue and peripheral blood samples to analyze potential biomarkers associated with efficacy, resistance, and safety.
|
Blood samples collected at baseline, Cycle 5 Day 1, and Cycle 8 Day 1 (21-day cycle); tumor tissue collected at baseline from archived FFPE blocks or fresh biopsy. Analysis cutoff at 6 months.
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- MA-BC-II-146
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.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .