Pirtobrutinib+Pola-R-CHP for Newly Diagnosed Non-GCB DLBCL
2026年8月4日 更新者:Lu Xuzhang、Changzhou No.2 People's Hospital
A Prospective, Multicenter Clinical Study of Pirtobrutinib Combined With Polatuzumab Vedotin, Rituximab, Cyclophosphamide, Doxorubicin and Prednisone (Pola-R-CHP) for Newly Diagnosed Non-GCB Diffuse Large B-Cell Lymphoma (DLBCL)
This is a single-arm, open-label, multicenter clinical study evaluating the efficacy and safety of pirtobrutinib combined with Pola-R-CHP in previously untreated Non-GCB DLBCL.
PET/CT assessment will be performed after 3 cycles of combination therapy.
Patients achieving CR/PR will continue treatment for another 3 cycles, while those with PD/SD will be discontinued from the study.
Patients achieving CR/PR after 6 cycles of treatment will undergo follow-up with PET/CT or contrast-enhanced CT every 3 months during the first year and every 6 months thereafter, until disease progression, death, withdrawal of informed consent, or study completion, whichever occurs first.
研究概览
研究类型
介入性
注册 (估计的)
48
阶段
- 阶段2
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Jianyong Li, PhD
- 邮箱:lijianyonglm@126.com
学习地点
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Jiangsu
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Nanjing、Jiangsu、中国
- Jiangsu Province Hospital The First Affiliated Hospital with Nanjing Medical University
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接触:
- Jianyong Li, PhD
- 邮箱:lijianyonglm@126.com
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-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Histologically confirmed Non-GCB DLBCL (per 2016 WHO diagnostic criteria);
- Whole-body PET/CT performed within 28 days prior to study enrollment demonstrating at least one measurable lesion (per 2014 Lugano criteria);
- Age 18-65 years, with expected survival >3 months;
- No prior anti-lymphoma treatment;
- Signed written informed consent and ability to comply with protocol-required visits and procedures;
- ECOG performance status 0-2;
Adequate organ and bone marrow function, defined as follows:
- Hematology: Absolute neutrophil count (ANC) ≥1×10⁹/L, platelet count (PLT) ≥50×10⁹/L, hemoglobin (HGB) ≥8.0 g/dL; no granulocyte colony-stimulating factor, platelet transfusion, or red blood cell transfusion within 7 days prior to testing;
- Hepatic function: Total bilirubin (TBIL) ≤1.5×upper limit of normal (ULN); Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5×ULN;
- Renal function: Serum creatinine (Cr) ≤1.5×ULN or creatinine clearance (CCR) ≥50 mL/min;
- Cardiac function: NYHA Class III or below; left ventricular ejection fraction ≥50% by echocardiography;
- Coagulation: International normalized ratio (INR) ≤1.5×ULN, activated partial thromboplastin time (APTT) ≤ULN +10s, and prothrombin time (PT) ≤ULN +3s;
- Women of childbearing potential or male subjects with partners of childbearing potential must use effective contraception throughout the treatment period and for 90 days after the last dose.
Exclusion Criteria:
- Central nervous system involvement;
- History of hypersensitivity to the study drug, drugs of the same class, or excipients;
- Concurrent malignancy requiring treatment or intervention;
- Major surgery within 4 weeks prior to treatment (excluding vascular access catheter placement or biopsy);
- Presence of any life-threatening disease, medical condition, or organ system dysfunction that, in the investigator's opinion, may affect patient safety or compliance with study procedures;
- Uncontrolled cardiac symptoms or disease, including: i. NYHA Class II or higher heart failure; ii. Unstable angina; iii. Myocardial infarction within 1 year; iv. Clinically significant supraventricular or ventricular arrhythmias requiring treatment or intervention;
- Active bleeding;
- Active, uncontrolled systemic bacterial, viral, fungal, or parasitic infection (excluding onychomycosis), or other clinically significant active disease process that, in the investigator's opinion, renders the patient unsuitable for clinical trial participation;
- Known history of human immunodeficiency virus (HIV) infection and/or acquired immunodeficiency syndrome;
- Exclusion of patients with active chronic hepatitis B or active hepatitis C. Patients with positive hepatitis B surface antigen, hepatitis B core antibody, or hepatitis C virus antibody at screening must undergo further HBV-DNA and HCV-RNA testing. Patients with stable hepatitis B (HBV-DNA <2500 copies/mL or 500 IU/mL) on antiviral therapy and cured hepatitis C patients (below the limit of detection) may be enrolled;
- Definitive history of neurological or psychiatric disorder, including epilepsy or dementia;
- Pregnant or lactating women;
- Receipt of other investigational agents within 1 month prior to first dose;
- Any other factors that, in the investigator's opinion, may affect the evaluation of efficacy or safety in this study.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 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:Pirtobrutinib+Pola-R-CHP for newly diagnosed non GCB DLBCL
This is a single-arm, open-label, multicenter clinical study evaluating the efficacy and safety of pirtobrutinib combined with Pola-R-CHP in previously untreated Non-GCB DLBCL.
PET/CT assessment will be performed after 3 cycles of combination therapy.
Patients achieving CR/PR will continue treatment for another 3 cycles, while those with PD/SD will be discontinued from the study.
Patients achieving CR/PR after 6 cycles of treatment will undergo follow-up with PET/CT or contrast-enhanced CT every 3 months during the first year and every 6 months thereafter, until disease progression, death, withdrawal of informed consent, or study completion, whichever occurs first.
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Pirtobrutinib 200 mg once daily Polatuzumab vedotin 1.8 mg/kg intravenously on Day 1 Rituximab 375 mg/m² on Day 1 Cyclophosphamide 750 mg/m² on Day 1 Doxorubicin 50 mg/m² on Day 1 Prednisone 100 mg on Days 1 to 5 Each cycle lasts 21 days.
PET/CT evaluation is conducted after 3 treatment cycles.
Subjects who attain CR or PR will receive an additional 3 cycles of therapy.
Subjects with PD or SD will be withdrawn from the study.
Subjects who do not achieve CR or PR upon completion of 6 cycles will be withdrawn from the study.
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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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2-year progression-free survival (PFS) rate
大体时间:2 years
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2 years
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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) after 6 cycles of induction therapy
大体时间:week 18,at the end of 6 cycles of induction therapy(each cycle is 21 days)
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week 18,at the end of 6 cycles of induction therapy(each cycle is 21 days)
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Complete Response Rate (CRR) after 6 cycles of induction therapy
大体时间:week 18, at the end of 6 cycles of induction therapy(each cycle is 21 days)
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week 18, at the end of 6 cycles of induction therapy(each cycle is 21 days)
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Overall Survival(OS)
大体时间:up to 4 years
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up to 4 years
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Number of participants with treatment-related adverse events (TRAEs) as assessed by CTCAE v5.0
大体时间:up to 4 years
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up to 4 years
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年7月31日
初级完成 (估计的)
2028年7月31日
研究完成 (估计的)
2030年7月31日
研究注册日期
首次提交
2026年7月30日
首先提交符合 QC 标准的
2026年7月30日
首次发布 (实际的)
2026年8月4日
研究记录更新
最后更新发布 (实际的)
2026年8月6日
上次提交的符合 QC 标准的更新
2026年8月4日
最后验证
2026年7月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.