SHR-A1811 Monotherapy or Sequential THPy as Neoadjuvant Therapy for Stage II-III HER2-Positive Breast Cancer
2026年8月24日 更新者:First Affiliated Hospital of Zhejiang University
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
This is a prospective, open-label, phase II, multicenter exploratory clinical study.
Eligible female patients aged 18-75 years with stage II-III HER2-positive breast cancer will receive 4 cycles of SHR-A1811 (4.8 mg/kg, intravenous infusion every 3 weeks).
After 4 cycles, tumor response will be assessed per RECIST 1.1 criteria.
Patients with a ≥50% reduction in tumor burden will continue with another 4 cycles of SHR-A1811 followed by definitive surgery.
Patients with <50% reduction will receive 4 cycles of the THPy regimen (docetaxel + trastuzumab + pyrotinib) before surgery.
Circulating tumor DNA (ctDNA) will be assessed for minimal residual disease (MRD) at baseline, after 4 cycles of treatment, and postoperatively.
The primary endpoint is total pathological complete response (tpCR), assessed by an independent review committee (IRC).
This study aims to evaluate the efficacy, safety, and feasibility of imaging- and MRD-guided neoadjuvant therapy in HER2-positive breast cancer.
調査の概要
状態
状態
まだ募集していません
条件
条件
介入・治療
介入・治療
研究の種類
研究の種類
介入
入学 (推定)
入学
80
段階
段階
- フェーズ2
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
研究連絡先
- 名前:Peifen Fu
- 電話番号:0571-87236852
- メール:Fupeifen@hotmail.com
研究場所
-
-
Zhejiang
-
Hangzhou、Zhejiang、中国、310003
- The First Affiliated Hospital, Zhejiang University School of Medicine
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主任研究者:
- Peifen Fu
-
コンタクト:
- Minya Yao
- 電話番号:13634111760
- メール:yminya@163.com
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主任研究者:
- Minya Yao
-
-
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
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
いいえ
説明
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.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
アーム数
1
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
実験的: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.
|
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.
|
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
|
Rate of total pathological complete response (tpCR)
時間枠: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)
|
二次結果の測定
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
Rate of breast pathological complete response (bpCR)
時間枠:At the time of definitive surgery (approximately 24 weeks after enrollment)
|
At the time of definitive surgery (approximately 24 weeks after enrollment)
|
|
Objective Response Rate (ORR)
時間枠: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)
|
その他の成果指標
その他の成果指標
結果測定 |
時間枠 |
|---|---|
|
Incidence and severity of Adverse Events (AEs)
時間枠:From first study drug administration up to 30 days after the last dose of study treatment
|
From first study drug administration up to 30 days after the last dose of study treatment
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (推定)
研究開始
2026年9月1日
一次修了 (推定)
一次修了
2029年4月1日
研究の完了 (推定)
研究の完了
2030年10月1日
試験登録日
最初に提出
最初に提出
2026年8月24日
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
2026年8月24日
最初の投稿 (実際)
最初の投稿
2026年8月26日
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
2026年8月26日
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
2026年8月24日
最終確認日
最終確認日
2026年8月1日
詳しくは
本研究に関する用語
その他の研究ID番号
その他の研究ID番号
- 26-OBU-ZJ-BC-II-020
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
いいえ
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
いいえ
米国FDA規制機器製品の研究
いいえ
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。