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.
調査の概要
状態
条件
研究の種類
入学 (推定)
連絡先と場所
研究連絡先
- 名前:Ting Li
研究連絡先のバックアップ
- 名前:Xiahong Wang
- 電話番号:8613524491606
- メール:whx365@126.com
研究場所
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Shanghai Municipality
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Shanghai、Shanghai Municipality、中国、200032
- 募集
- Fudan University Shanghai Cancer Center
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コンタクト:
- Hongxia wang, PHD
- 電話番号:021-64175590
- メール:whx365@126.com
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コンタクト:
- メール:whx365@126.com
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
サンプリング方法
調査対象母集団
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
コホートと介入
グループ/コホート |
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Phase 1(Model Building Cohort)
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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. |
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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Sensitivity and specificity of sEVs-specific markers for breast cancer molecular subtyping diagnosis
時間枠:From baseline through treatment completion, up to 36 months
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Sensitivity and specificity of sEVs-specific markers for breast cancer molecular subtyping diagnosis
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From baseline through treatment completion, up to 36 months
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Distribution of sEVs molecular subtypes
時間枠:From baseline through treatment completion, up to 36 months
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Distribution of sEVs molecular subtypes
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From baseline through treatment completion, up to 36 months
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Correlation analysis between sEVs molecular subtypes and drug efficacy
時間枠:From baseline through treatment completion, up to 36 months
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Correlation analysis between sEVs molecular subtypes and drug efficacy
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From baseline through treatment completion, up to 36 months
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PFS (Progression-Free Survival)
時間枠:From treatment initiation until progression or death, up to 36 months
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Time from start of treatment to the first documented disease progression per RECIST v1.1 or death due to any cause.
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From treatment initiation until progression or death, up to 36 months
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Overall Survival (OS) and Objective Response Rate (ORR)
時間枠:From treatment initiation until progression or death , up to 36 months
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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
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Safety and Tolerability of Physician-Selected Treatment Regimens
時間枠:From treatment initiation until 30 days after the last dose, or until the initiation of a new antineoplastic therapy, whichever occurs first.
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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.
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From treatment initiation until 30 days after the last dose, or until the initiation of a new antineoplastic therapy, whichever occurs first.
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協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
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