- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07574749
Molecular Subtyping of Breast Cancer-derived Small Extracellular Vesicles (sEVs) to Predict Therapeutic Efficacy
Molecular Subtyping of Breast Cancer-derived Small Extracellular Vesicles (sEVs) to Predict Therapeutic Efficacy: An Exploratory, Single-Center, Phase II Clinical Study
The goal of this observational study is to learn if a new diagnostic test using specific labels for breast cancer sEVs on a microchip can accurately diagnose the molecular subtypes in patients with breast cancer. The main questions it aims to answer are:
- What is the sensitivity of this new sEVs-based panel for diagnosing breast cancer molecular subtypes?
- What is the specificity of this new sEVs-based panel for diagnosing breast cancer molecular subtypes? Researchers will compare the results from the new sEVs panel to the results from the standard pathological diagnosis to see if the new panel is accurate and reliable.
Participants will be asked to:
- Provide blood samples and tissue samples.
- Allow researchers to access their clinical data, such as their diagnosis, treatment information, and outcomes.
Visão geral do estudo
Status
Condições
Tipo de estudo
Inscrição (Estimado)
Contactos e Locais
Contato de estudo
- Nome: Ting Li
Estude backup de contato
- Nome: Xiahong Wang
- Número de telefone: 8613524491606
- E-mail: whx365@126.com
Locais de estudo
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, China, 200032
- Recrutamento
- Fudan University Shanghai Cancer Center
-
Contato:
- Hongxia wang, PHD
- Número de telefone: 021-64175590
- E-mail: whx365@126.com
-
Contato:
- E-mail: whx365@126.com
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Método de amostragem
População do estudo
Descrição
Inclusion Criteria:
- Age 18-75 years (inclusive)
- ECOG performance status 0-1
- Life expectancy ≥3 months
- Unresectable or metastatic breast cancer
- Core needle biopsy of recurrent/metastatic lesions is ongoing or planned before initiating new treatment regimen, with provision of fresh tumor tissue specimens and collection of peripheral blood samples
- Per RECIST v1.1 criteria, at least one measurable lesion or bone-only metastases
Adequate bone marrow reserve and organ function prior to first dose:
- Bone marrow reserve: Platelet count (PLT) ≥90 × 10⁹/L, absolute neutrophil count (ANC) ≥1.5 × 10⁹/L, hemoglobin ≥9 g/dL
- Coagulation function: INR ≤1.5, APTT ≤1.5 × ULN
- Hepatic function: Basically normal liver function, total bilirubin ≤1.5 × ULN (patients with Gilbert's syndrome may have total bilirubin ≤3 × ULN), AST and ALT ≤2.5 × ULN (if liver metastases are present, AST and ALT ≤5 × ULN)
- Renal function: Serum creatinine ≤1.5 × ULN or creatinine clearance ≥50 mL/min (calculated by Cockcroft-Gault formula)
- Cardiac function: Left ventricular ejection fraction (LVEF) ≥50%; QTcF ≤470 ms for females, ≤450 ms for males Able to communicate effectively with the investigator and understand and comply with all requirements of the study -
Exclusion Criteria:
- Receipt of radiotherapy, chemotherapy, traditional Chinese medicine with anti-tumor indications, or local therapy (interventional treatment but excluding tumor biopsy, ablation therapy, etc.) within 2 weeks prior to enrollment
- Adverse reactions from previous anti-tumor treatment not recovered to ≤Grade 1 per CTCAE v5.0 (except for toxicities judged by the investigator to have no safety risk, such as alopecia, long-term toxicities from radiotherapy, or other toxicities ≤Grade 2)
- Other malignancies within the past 5 years, excluding cured cervical carcinoma in situ, basal cell carcinoma of the skin, or squamous cell carcinoma of the skin
- Uncontrolled or serious medical conditions, including but not limited to active infections requiring systemic antibiotic therapy
History of serious cardiovascular or cerebrovascular diseases, including but not limited to:
- Serious cardiac rhythm or conduction abnormalities, such as ventricular arrhythmias requiring clinical intervention, second- to third-degree atrioventricular block, etc.
- Class III-IV cardiac dysfunction per New York Heart Association (NYHA) criteria
- Acute coronary syndrome, congestive heart failure, aortic dissection, stroke, or other Grade ≥3 cardiovascular or cerebrovascular events within 6 months prior to first dose
- Clinically uncontrolled hypertension
- Any factors that increase the risk of QTc prolongation or arrhythmias, such as heart failure, hypokalemia, congenital long QT syndrome, or use of any concomitant medications known or suspected to prolong the QT interval
- History of immunodeficiency, including other acquired or congenital immunodeficiency diseases, or history of organ transplantation, allogeneic bone marrow transplantation, or autologous hematopoietic stem cell transplantation
HIV infection, active HBV or HCV infection; the following situations are allowed for enrollment:
- Patients positive for hepatitis B surface antigen (HBsAg), with or without positive hepatitis B core antibody (anti-HBc), if HBV DNA <500 IU/mL or below the lower limit of the study site's reference range, and active infection is ruled out by the investigator based on clinical treatment, presentation, etc.
- Patients positive for hepatitis C (HCV) antibody when HCV RNA is negative
- Females of childbearing potential with positive pregnancy test within 7 days prior to first dose or who are lactating
- Known psychiatric illness or disorder that may affect study compliance
- Other conditions judged by the investigator to be unsuitable for participation in this study
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
Coortes e Intervenções
Grupo / Coorte |
|---|
|
Phase 1(Model Building Cohort)
|
|
Phase 1(Model Building Cohort), Phase 2(External Validation Cohort)
Phase 1(Model Building Cohort): 500 participants will be enrolled to construct a classifier composed of sEVs molecules as a predictive model for molecular subtyping. Phase 2(External Validation Cohort): 1,000 participants will be enrolled to evaluate the sensitivity and specificity of sEVs-specific markers for breast cancer molecular subtyping diagnosis compared with classical pathological molecular subtyping diagnosis using ROC curves and other tools. This phase will delineate the distribution of sEVs molecular subtypes and explore the correlation between sEVs molecular subtypes and the efficacy of treatment regimens selected by physicians. |
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Sensitivity and specificity of sEVs-specific markers for breast cancer molecular subtyping diagnosis
Prazo: From baseline through treatment completion, up to 36 months
|
Sensitivity and specificity of sEVs-specific markers for breast cancer molecular subtyping diagnosis
|
From baseline through treatment completion, up to 36 months
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Distribution of sEVs molecular subtypes
Prazo: From baseline through treatment completion, up to 36 months
|
Distribution of sEVs molecular subtypes
|
From baseline through treatment completion, up to 36 months
|
|
Correlation analysis between sEVs molecular subtypes and drug efficacy
Prazo: From baseline through treatment completion, up to 36 months
|
Correlation analysis between sEVs molecular subtypes and drug efficacy
|
From baseline through treatment completion, up to 36 months
|
|
PFS (Progression-Free Survival)
Prazo: From treatment initiation until progression or death, up to 36 months
|
Time from start of treatment to the first documented disease progression per RECIST v1.1 or death due to any cause.
|
From treatment initiation until progression or death, up to 36 months
|
|
Overall Survival (OS) and Objective Response Rate (ORR)
Prazo: From treatment initiation until progression or death , up to 36 months
|
Objective Response Rate (ORR): As assessed according to the RESIST 1.1 criteria, with complete response (CR) and partial response (PR) combined to define a response. Overall Survival (OS): The time from enrolment to death from any cause; for lost-to-follow-up patients, survival is calculated as of the date of the last follow-up visit, and these are treated as censored data. |
From treatment initiation until progression or death , up to 36 months
|
|
Safety and Tolerability of Physician-Selected Treatment Regimens
Prazo: From treatment initiation until 30 days after the last dose, or until the initiation of a new antineoplastic therapy, whichever occurs first.
|
All subjects shall undergo toxicity assessment from the start of their first treatment, with toxicity assessed using the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0.
|
From treatment initiation until 30 days after the last dose, or until the initiation of a new antineoplastic therapy, whichever occurs first.
|
Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- sEVs-ABC-IIT-001
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .