Albumin-bound Paclitaxel (Ⅱ)-Combined Regimens for Pancreatic Cancer
A Multi-cohort Exploratory Study to Evaluate the Efficacy and Safety of Albumin-bound Paclitaxel (Ⅱ)-Combined Regimens for Pancreatic Cancer
This is a prospective, multi-center, multi-cohort exploratory study. Cohort 1 enrolls 39 patients with unresectable locally advanced or metastatic pancreatic cancer, who will receive first-line treatment with cisplatin plus nab-paclitaxel (Ⅱ), capecitabine, and gemcitabine (PAXG).
Cohort 2 enrolls 27 patients with borderline-resectable or high-risk resectable pancreatic cancer, who will receive neoadjuvant therapy with the PAXG regimen.
Cohort 3 enrolls patients with pancreatic cancer who have undergone curative resection, who will receive adjuvant therapy with nab-paclitaxel (Ⅱ), capecitabine, and gemcitabine.
Objectives of Study: To evaluate the efficacy and safety of nab-paclitaxel (Ⅱ)-based regimes for pancreatic cancer.
研究概览
地位
条件
研究类型
注册 (估计的)
阶段
- 阶段2
联系人和位置
学习联系方式
- 姓名:Jihui Hao
- 电话号码:022-2340123-3077
- 邮箱:18622221120@163.com
学习地点
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Tianjin、中国
- Tianjin Medical University Cancer Institute & Hospital
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Aged 18 to 75 years old.
- Histopathologically confirmed pancreatic adenocarcinoma meeting any one of the following conditions: (1) Unresectable locally advanced or metastatic pancreatic cancer, with no prior systemic anti-tumor therapy for advanced disease. Prior neoadjuvant/adjuvant chemotherapy is permitted, provided the interval from completion of prior chemotherapy to study drug administration is more than 6 months. (2) High-risk resectable or borderline resectable pancreatic cancer assessed by a multidisciplinary team.(3) Curative resection (R0 or R1 resection) performed without prior neoadjuvant therapy, and adjuvant treatment can be initiated within 12 weeks postoperatively.
- Presence of at least one measurable lesion per RECIST v1.1 (exclusive to participants in Cohort 3).
- Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1.
- Estimated survival time ≥ 3 months.
- Adequate bone marrow function: absolute neutrophil count (ANC) ≥ 1.5×10⁹/L, platelet count (PLT) ≥ 100×10⁹/L, hemoglobin (Hb) ≥ 90 g/L.
- Adequate liver function: alanine transaminase (ALT) and aspartate transaminase (AST) ≤ 2.5×ULN (≤5×ULN allowed in patients with liver metastases); total bilirubin ≤ 1.5×ULN.
- Adequate renal function: serum creatinine (Cr) ≤ 1.5×ULN, or creatinine clearance ≥ 60 mL/min (calculated by Cockroft-Gault formula).
- Adequate coagulation function: prothrombin time (PT) and activated partial thromboplastin time (APTT) ≤ 1.5×ULN.
- Women of childbearing potential must have a negative serum/urine pregnancy test within 14 days prior to enrollment, be non-lactating, and agree to use effective contraception throughout the study and for 6 months after the last study treatment. Male participants must agree to effective contraception during the study and for 6 months after study completion.
- Able to understand the study information; participant or legal representative voluntarily provides written informed consent.
Exclusion Criteria:
- History of other malignant tumors within the past 5 years
- Known hypersensitivity or intolerance to any study drug or excipients.
- Confirmed homozygous or compound heterozygous DPYD variants leading to complete dihydropyrimidine dehydrogenase (DPD) deficiency.
- Presence of any of the following comorbidities: ① Severe or uncontrolled cardiovascular disease: New York Heart Association (NYHA) Class II or higher chronic heart failure, uncontrolled hypertension (systolic BP >150 mmHg and/or diastolic BP >90 mmHg despite stable medication), etc. ② Severe respiratory disorders: asthma requiring inhaled/systemic glucocorticoids, active chronic obstructive pulmonary disease, etc. ③ Confirmed neurological diseases (epilepsy, dementia, etc.) or Grade ≥2 peripheral sensory/motor neuropathy. ④ Uncontrolled diabetes mellitus (fasting blood glucose ≥10 mmol/L under stable treatment). ⑤ Severe chronic or active infections requiring ≥1 consecutive week of systemic antibacterial, antifungal or antiviral therapy (including tuberculosis). ⑥ Active HIV infection (HIV antibody positive); untreated active HBV (HBsAg/HBcAg positive with HBV-DNA above institutional upper limit of normal) or active HCV infection (HCV antibody positive with HCV-RNA above institutional upper limit of normal).
- Untreated active brain metastases (including symptomatic brain or leptomeningeal metastases). Participants with brain metastases are eligible only if brain lesions are stable on imaging performed ≥4 weeks prior to first study dose, no new neurological symptoms or baseline symptom relapse, and no systemic steroid administration for ≥14 days before study treatment initiation, with no evidence of new or enlarged metastatic lesions.
- Medical history as follows: ① Major abdominal/thoracic surgery within 28 days prior to first study dose, or planned major surgery during the study period (diagnostic puncture and infusion port implantation excluded). ② Severe cardiovascular/cerebrovascular events (myocardial infarction, unstable angina, cerebrovascular accident) within 6 months prior to enrollment; clinically silent lacunar infarcts are permitted.
- History of deep vein thrombosis or pulmonary embolism within 3 months prior to enrollment.
- Inability to swallow or untreated malabsorption syndrome.
- Receipt of any investigational product within 1 month prior to enrollment.
- Any other condition judged by the investigator to render the participant unsuitable for study participation.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:非随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:Chort 1
Cisplatin + Albumin-bound Paclitaxel (Ⅱ) + Capecitabine + Gemcitabine, q2w, Treatment will continue until disease progression or intolerable toxicity.
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Cisplatin: 30 mg/m² , d1
Albumin-bound Paclitaxel (Ⅱ): 150 mg/m² , d1
Albumin-bound Paclitaxel (Ⅱ): 100/125 mg/m² , d1, d8
Capecitabine 625 mg/m²,po,bid, d1-14
Capecitabine 1660 mg/(m² • d), d1-14
Gemcitabine 800 mg/m², d1
Gemcitabine 1000 mg/m², d1, d8
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实验性的:Chort 2
Cisplatin + Albumin-bound Paclitaxel (Ⅱ) + Capecitabine + Gemcitabine, q2w, with a maximum of 12 treatment cycles.
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Cisplatin: 30 mg/m² , d1
Albumin-bound Paclitaxel (Ⅱ): 150 mg/m² , d1
Albumin-bound Paclitaxel (Ⅱ): 100/125 mg/m² , d1, d8
Capecitabine 625 mg/m²,po,bid, d1-14
Capecitabine 1660 mg/(m² • d), d1-14
Gemcitabine 800 mg/m², d1
Gemcitabine 1000 mg/m², d1, d8
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实验性的:Chort 3
Albumin-bound Paclitaxel (Ⅱ) + Capecitabine + Gemcitabine, q3w, for a total treatment duration of up to 6 months.
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Albumin-bound Paclitaxel (Ⅱ): 150 mg/m² , d1
Albumin-bound Paclitaxel (Ⅱ): 100/125 mg/m² , d1, d8
Capecitabine 625 mg/m²,po,bid, d1-14
Capecitabine 1660 mg/(m² • d), d1-14
Gemcitabine 800 mg/m², d1
Gemcitabine 1000 mg/m², d1, d8
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
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Progression-Free Survival (PFS)
大体时间:Time from subject's first study drug administration to first documented disease progression (per RECIST v1.1) or death from any cause, whichever occurs first, assessed up to 5.5 months.
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Time from subject's first study drug administration to first documented disease progression (per RECIST v1.1) or death from any cause, whichever occurs first, assessed up to 5.5 months.
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1-Year Event-Free Survival Rate (1y-EFS Rate)
大体时间:12 months after signing informed consent, until first EFS event or loss to follow-up.
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12 months after signing informed consent, until first EFS event or loss to follow-up.
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Recommended Phase 2 Dose (RP2D)
大体时间:After all participants in each dose cohort complete the 21-day DLT observation period.
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After all participants in each dose cohort complete the 21-day DLT observation period.
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Disease-Free Survival (DFS)
大体时间:From informed consent signature to tumor recurrence or all-cause death (whichever occurs first), assessed up to 20 months.
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From informed consent signature to tumor recurrence or all-cause death (whichever occurs first), assessed up to 20 months.
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次要结果测量
结果测量 |
大体时间 |
|---|---|
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Objective Response Rate (ORR)
大体时间:Tumor response assessment every 8 weeks (±7 days) after first study drug administration until disease progression, death or end-of-follow-up, assessed up to 5.5 months.
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Tumor response assessment every 8 weeks (±7 days) after first study drug administration until disease progression, death or end-of-follow-up, assessed up to 5.5 months.
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Maximum Tolerated Dose (MTD)
大体时间:After DLT observation completion and RP2D determination for all dose cohorts, assessed up to 1 months.
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After DLT observation completion and RP2D determination for all dose cohorts, assessed up to 1 months.
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R0 Resection Rate
大体时间:After neoadjuvant therapy completion, at pathological report of surgical specimen, assessed up to 7 months.
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After neoadjuvant therapy completion, at pathological report of surgical specimen, assessed up to 7 months.
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Incidence of Adverse Events
大体时间:From the time of informed consent signature through 30 days after last study drug administration.
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From the time of informed consent signature through 30 days after last study drug administration.
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Disease Control Rate (DCR)
大体时间:Tumor response assessment every 8 weeks (±7 days) after first study drug administration until disease progression, death or end-of-follow-up, assessed up to 5.5 months..
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Tumor response assessment every 8 weeks (±7 days) after first study drug administration until disease progression, death or end-of-follow-up, assessed up to 5.5 months..
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Overall Survival (OS)
大体时间:Time from subject's first study drug administration to death from any cause, assessed up to 40 months.
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Time from subject's first study drug administration to death from any cause, assessed up to 40 months.
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Dose-Limiting Toxicity (DLT)
大体时间:After all participants in each dose cohort complete the 21-day DLT observation period.
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After all participants in each dose cohort complete the 21-day DLT observation period.
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Event-Free Survival (EFS)
大体时间:From informed consent signature to first local recurrence, distant metastasis, tumor progression, second malignancy or all-cause death (whichever occurs first), assessed up to 16 months.
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From informed consent signature to first local recurrence, distant metastasis, tumor progression, second malignancy or all-cause death (whichever occurs first), assessed up to 16 months.
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Major Pathological Response (MPR) Rate
大体时间:Upon completion of pathological diagnosis of resected surgical specimen, assessed up to 7 months.
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Upon completion of pathological diagnosis of resected surgical specimen, assessed up to 7 months.
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Pathological Complete Response (pCR) Rate
大体时间:Upon completion of pathological diagnosis of resected surgical specimen, assessed up to 7 months.
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Upon completion of pathological diagnosis of resected surgical specimen, assessed up to 7 months.
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Duration of Response (DOR)
大体时间:Time from first documented CR or PR to subsequent disease progression or death from any cause, whichever occurs first, until end-of-follow-up, assessed up to 6 months.
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Time from first documented CR or PR to subsequent disease progression or death from any cause, whichever occurs first, until end-of-follow-up, assessed up to 6 months.
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- CSPC-XBZ-PC-K03
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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