Exploratory Study on the Efficacy and Safety of Trastuzumab Rezetecan in the Treatment of HER2-Expressiong Advanced Solid Tumor
The goal of this clinical trial is to learn if Trastuzumab Rezetecan can treat advanced solid tumors with HER-2 expression in adult participants.
The main question it aims to answer is: What is the objective response rate of Trastuzumab Rezetecan in adult patients with HER-2 expressed advanced solid tumors? Participants will receive intravenous infusion of Trastuzumab Rezetecan on Day 1 of each 21-day treatment cycle. The dosage is 4.8 mg/kg per cycle; participants with a body weight of 85 kg or above will receive a fixed dose of 408 mg every 3 weeks.
調査の概要
状態
条件
介入・治療
研究の種類
入学 (推定)
段階
- フェーズ2
連絡先と場所
研究連絡先
- 名前:Haihua Yuan
- 電話番号:+86-021-56691101-7261
- メール:ayuan790415@shsmu.edu.cn
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
説明
Inclusion Criteria:
- Male and female participants aged 18 years or older.
- Participants with locally advanced, unresectable or metastatic solid tumors who have progressed after at least one prior systemic therapy for advanced/metastatic disease, or have no satisfactory alternative treatment options. Eligible tumor types include but are not limited to biliary tract cancer, endometrial cancer, urothelial carcinoma, pancreatic cancer, colorectal cancer, gastric cancer, non-small cell lung cancer, head and neck adenocarcinoma (salivary gland adenocarcinoma, lacrimal gland adenocarcinoma, adenocarcinoma of unknown primary in the neck), cervical cancer, ovarian cancer and adenocarcinoma of unknown primary. Breast cancer is excluded.
- Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 or 1.
- Confirmed HER2 expression defined as IHC 1+, 2+ or 3+ (per GC criteria).
- Willing and able to provide adequate tumor specimens for central pathological re-testing of HER2 status. For participants previously treated with anti-HER2 therapy, tumor specimens obtained after the last anti-HER2 treatment are optional.
- At least one measurable lesion at baseline per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
Adequate organ and bone marrow function within 14 days prior to enrollment, meeting the following criteria:
Hemoglobin ≥ 9 g/dL; Platelet count ≥ 100,000/mm³; Absolute neutrophil count (ANC) ≥ 1500/mm³; Serum albumin ≥ 3.0 g/dL; Prothrombin time (PT), activated partial thromboplastin time (aPTT) and International Normalized Ratio (INR) ≤ 1.5 × upper limit of normal (ULN); Aspartate transaminase (AST) and alanine transaminase (ALT) ≤ 3 × ULN; ≤ 5 × ULN for participants with liver metastases; Total bilirubin ≤ 1.5 × ULN for participants without liver metastases; ≤ 3 × ULN for participants with Gilbert's syndrome or liver metastases at baseline; Creatinine clearance ≥ 30 mL/min (calculated by the Cockcroft-Gault formula)
- Left ventricular ejection fraction (LVEF) ≥ 50% assessed by echocardiogram (ECHO) or multigated acquisition (MUGA) scan within 28 days prior to enrollment.
Exclusion Criteria:
Participants meeting any of the following conditions are ineligible for this study:
Presence of any severe and/or uncontrolled diseases:
- Poorly controlled blood pressure (systolic blood pressure ≥ 150 mmHg or diastolic blood pressure ≥ 100 mmHg); poorly controlled diabetes (fasting blood glucose [FBG] > 10 mmol/L).
- Grade ≥ 2 myocardial ischemia, myocardial infarction, arrhythmia (QTc interval ≥ 470 ms), or Grade ≥ 2 congestive heart failure (per New York Heart Association [NYHA] classification).
- Active or uncontrolled severe infections (Grade ≥ 2 per NCI CTCAE) requiring systemic antibacterial, antifungal or antiviral therapy, including pulmonary tuberculosis.
- History of active tuberculosis.
- Uncontrolled ascites, pericardial effusion or pleural effusion requiring repeated drainage.
- Active hepatitis: Liver function not meeting the inclusion criteria. Hepatitis B: HBV DNA ≥ 2000 IU/mL or ≥ 10^4 copies/mL.Hepatitis C: HCV RNA ≥ 2000 IU/mL or ≥ 10^4 copies/mL. Participants with viral load below the above thresholds after nucleoside antiviral therapy are eligible. Chronic hepatitis B virus carriers with HBV DNA < 10^4 IU/mL must receive concurrent antiviral treatment throughout the study for enrollment.
- History of immunodeficiency diseases, including HIV positivity or other acquired/congenital immunodeficiency disorders.
- History of allogeneic solid organ transplantation or allogeneic hematopoietic stem cell transplantation.
- Confirmed meningeal metastasis, spinal cord metastasis or spinal cord compression.
- Within 6 months prior to the first study drug administration, presence of esophageal gastric varices, severe ulcers, unhealed wounds, gastrointestinal perforation, abdominal fistula, gastrointestinal obstruction, intra-abdominal abscess, acute gastrointestinal bleeding, extensive intestinal resection (partial colectomy or extensive small bowel resection complicated with chronic diarrhea), Crohn's disease, ulcerative colitis or long-standing chronic diarrhea.
- Unhealed or poorly healing wounds, or active ulcers.
- Toxicities from prior anti-tumor therapy have not resolved to Grade 0 or 1 per NCI CTCAE version 5.0.
- Received major surgery, incisional biopsy or significant traumatic injury within 28 days before study treatment initiation; or with long-standing unhealed wounds or fractures.
- History of severe hypersensitivity reactions to monoclonal antibodies; known allergy to the active ingredients or excipients of the study drug.
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
- 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)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Trastuzumab Rezetecan
Participants will receive intravenous infusion of Trastuzumab Rezetecan on Day 1 of each 21-day treatment cycle.
The dosage is 4.8 mg/kg per cycle; participants with a body weight of 85 kg or above will receive a fixed dose of 408 mg every 3 weeks.
|
Trastuzumab Rezetecan will be administered on Day 1 of each 21-day cycle as specified.
The dose is 4.8 mg/kg (fixed 408 mg for body weight ≥85 kg).
Treatment continues until tumor progression or occurrence of unacceptable toxicity.
|
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 |
|---|---|---|
|
Objective Response Rate, ORR
時間枠:From the date of first study treatment until disease progression or death from any cause, whichever occurs first, assessed up to 24months.
|
The Objective Response Rate (ORR) is defined as the percentage of patients whose best response on or before the first occurrence of disease progression is a complete response (CR) or partial response (PR).
Tumor responses were assessed by investigators using Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
|
From the date of first study treatment until disease progression or death from any cause, whichever occurs first, assessed up to 24months.
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Duration of Response, DOR
時間枠:From the date of first documented response (complete response [CR] or partial response [PR]) to the time of disease progression or death from any cause, whichever occurs first, assessed up to 24months.
|
Duration of Response (DoR) is defined as the time from the date of first documented response (CR or PR) to date of first occurrence of disease progression as determined by the investigator, or death from any cause, whichever occurs first.
|
From the date of first documented response (complete response [CR] or partial response [PR]) to the time of disease progression or death from any cause, whichever occurs first, assessed up to 24months.
|
|
Progression-Free Survival, PFS
時間枠:Through study completion, an average of 2 years.
|
Progression-Free Survival (PFS) is defined as the time from the start of study treatment to the first occurrence of disease progression, or death, whichever occurs first.
Tumor responses were assessed by investigators using RECIST version 1.1.
|
Through study completion, an average of 2 years.
|
|
Overall Survival, OS
時間枠:Through study completion, an average of 2 years.
|
Overall Survival (OS) is defined as the time from the date of the first study treatment (Day 1) to the date of death from any cause.
|
Through study completion, an average of 2 years.
|
|
Disease Control Rate, DCR
時間枠:From the date of first study treatment until disease progression or death from any cause, whichever occurs first, assessed up to 24 months.
|
Disease Control Rate (DCR) is defined as the proportion of patients whose best response is CR, PR or SD maintained more than 8 weeks.
Tumor responses were assessed by investigators using RECIST version 1.1.
|
From the date of first study treatment until disease progression or death from any cause, whichever occurs first, assessed up to 24 months.
|
|
Best Overall Response, BOR
時間枠:Through study completion, average follow-up of 2 years.
|
Best overall response (BOR) is defined as the best tumor response achieved at any time during treatment, categorized as Complete Response (CR), Partial Response (PR), Stable Disease (SD), or Progressive Disease (PD) per RECIST 1.1 criteria.
|
Through study completion, average follow-up of 2 years.
|
|
Time to Response, TTR
時間枠:Through study completion.
|
Time to response (TTR) is defined as the time from the date of first study drug administration to the date of first documented and confirmed CR or PR per RECIST 1.1.
|
Through study completion.
|
|
Patient-reported outcomes, PROs
時間枠:Baseline and every 12 weeks during treatment.
|
Patient-reported quality of life changes measured by the EORTC QLQ-C30 questionnaire.
Questionnaires are completed at baseline and repeated every 12 weeks during treatment to evaluate changes in patients' quality of life over time.
|
Baseline and every 12 weeks during treatment.
|
|
Adverse Events, AEs
時間枠:From first study drug administration through 40 days after the last dose; overall average follow-up duration is 2 years.
|
Incidence, severity (graded per NCI CTCAE version 5.0), and causality of adverse events (AEs).
|
From first study drug administration through 40 days after the last dose; overall average follow-up duration is 2 years.
|
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 (推定)
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
本研究に関する用語
キーワード
追加の関連 MeSH 用語
- 泌尿生殖器疾患
- 生殖器疾患
- 内分泌系疾患
- 病理学的プロセス
- 泌尿生殖器腫瘍
- 部位別新生物
- 女性の泌尿生殖器疾患
- 女性の泌尿生殖器疾患と妊娠合併症
- 腸の病気
- 気道疾患
- 組織型別の新生物
- 消化器腫瘍
- 消化器系腫瘍
- 消化器系疾患
- 消化器疾患
- 胃の病気
- 腸の腫瘍
- 直腸疾患
- 子宮の病気
- 生殖器疾患、女性
- 肺疾患
- 内分泌腺腫瘍
- 膵臓の病気
- 胆道疾患
- 新生物、腺および上皮
- 気道腫瘍
- 胸部腫瘍
- 結腸疾患
- 腫瘍性プロセス
- 肺新生物
- 性器腫瘍、女性
- がん
- 子宮頸部疾患
- がん、気管支原性
- 気管支腫瘍
- 子宮腫瘍
- 病理学的状態、徴候および症状
- 新生物
- 胃の新生物
- 胆道腫瘍
- 結腸直腸腫瘍
- 新生物転移
- 膵臓の新生物
- がん、非小細胞肺
- 子宮頸部腫瘍
- 頭頸部腫瘍
- 子宮内膜腫瘍
- がん、移行細胞
その他の研究ID番号
- JY2026-039
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?
IPD プランの説明
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
米国FDA規制機器製品の研究
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