A Multicenter, Prospective, Open-Label, Randomized Controlled Clinical Study of Orelabrutinib Combined With Obinutuzumab and Lenalidomide Versus Obinutuzumab Plus Chemotherapy for Treatment-Naive Follicular Lymphoma
研究概览
地位
条件
研究类型
注册 (估计的)
阶段
- 第三阶段
联系人和位置
学习联系方式
- 姓名:Peng-Peng Xu
- 电话号码:+862164370045 Ext. 610707
- 邮箱:pengpeng_xu@126.com
学习地点
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Shanghai Municipality
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Shanghai、Shanghai Municipality、中国、20025
- Ruijin Hosiptal
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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:
- Subjects with histopathologically confirmed follicular lymphoma (FL) Grade 1-3A;
- Subjects who have never received prior anti-lymphoma therapy;
- Age ≥ 18 years old;
- Eastern Cooperative Oncology Group (ECOG) performance status score of 0-2;
- Adequate bone marrow, hepatic and renal function, defined as:
1)Absolute neutrophil count (ANC) > 1,000/μL; platelet count > 50,000/mm³; hemoglobin > 80 g/dL; 2)Alanine transaminase (ALT) and aspartate transaminase (AST) < 3 × upper limit of normal (ULN); 3)Total serum bilirubin < 1.5 × ULN (patients with Gilbert syndrome are eligible); serum creatinine < 2 × ULN OR creatinine clearance > 50 mL/min; 6、Tumor tissue available for testing (fresh tissue preferred; archived paraffin-embedded tissue is acceptable); 7、Women of childbearing potential with a negative pregnancy test prior to Day 1 of treatment, who agree to use effective contraception throughout the study period and for at least 1 year after completion of study treatment; 8、Written informed consent obtained from the subject or their legal authorized representative prior to any study-specific examinations or procedures.
Exclusion Criteria:
- Uncontrolled cardiovascular and cerebrovascular diseases, coagulation disorders, connective tissue diseases, severe infectious diseases, etc.
Abnormal laboratory parameters at screening (unless attributed to follicular lymphoma):
- Absolute neutrophil count < 1.5 × 10⁹/L
- Platelet count < 80 × 10⁹/L; if bone marrow involvement is present, platelet count < 50 × 10⁹/L
- Alanine transaminase (ALT) or aspartate transaminase (AST) > 2 × upper limit of normal (ULN); alkaline phosphatase (AKP) or bilirubin > 1.5 × ULN
- Serum creatinine > 1.5 × ULN OR estimated glomerular filtration rate (eGFR) < 40 mL/min/1.73 m² (calculated via the Cockcroft-Gault equation or Modification of Diet in Renal Disease [MDRD] equation)
- Human immunodeficiency virus (HIV)-positive subjects.
- Left ventricular ejection fraction (LVEF) < 50%.
- HBV screening requirements: Subjects with positive hepatitis B surface antigen (HBsAg) must undergo HBV DNA testing; those with HBV DNA < 10³ IU/mL are eligible for enrollment. Subjects with negative HBsAg but positive hepatitis B core antibody (HBcAb) (regardless of hepatitis B surface antibody [HBsAb] status) must also undergo HBV DNA testing; those with HBV DNA < 10³ IU/mL are eligible for enrollment.
- Receiving concurrent anti-tumor therapy (for lymphoma or other malignancies).
- Subjects with psychiatric disorders, or those with known/suspected poor compliance to the study protocol.
- Requiring continuous treatment with strong or moderate CYP3A inhibitors or CYP3A inducers (see Appendix 3). Subjects who have taken strong/moderate CYP3A inhibitors or inducers within 7 days prior to the first dose of study drug (or within less than 5 half-lives of such medications) are excluded.
- History of stroke or intracranial hemorrhage within 6 months before the first dose of study drug.
- Inability to swallow capsules, or presence of diseases that significantly impair gastrointestinal function, such as malabsorption syndrome, bariatric surgery, inflammatory bowel disease, partial or complete intestinal obstruction.
Other uncontrolled concomitant medical conditions deemed by the investigator to interfere with study participation. Any life-threatening disease, medical condition or organ dysfunction that may compromise subject safety, interfere with the absorption or metabolism of oral targeted agents, or expose study outcomes to excessive risk, as judged by the investigator.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配: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:RO2
Patients in the study group will receive six cycles of the RO2 regimen, with each cycle repeated every 21 days. Routine efficacy assessments will be performed upon completion of each cycle during treatment. PET-CT scanning will be used for efficacy evaluation after three cycles of therapy. Patients with stable disease (SD) or progressive disease (PD) will discontinue study treatment, and the investigator will determine the salvage therapy regimen. Patients achieving a complete response (CR) or partial response (PR) will continue the original regimen for cycles 4 to 6. After completion of six cycles of treatment, PET-CT will be conducted for efficacy reassessment. Patients with CR or PR will finish induction therapy and enter the maintenance phase. The study group will receive obinutuzumab maintenance therapy once every three months for a total of two years, combined with lenalidomide maintenance administered for 10 days per month over six months. |
来那度胺 PO 将按照各自臂中指定的时间表进行管理。
Orelabrutinib PO 将按照各自手臂中指定的时间表进行管理。
Obinutuzumab IV infusion will be administered as per the schedule specified in the respective arm.
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有源比较器:O-Chemo
Patients in the study group will receive six cycles of the O-chemo regimen, with each cycle repeated every 21 days. Routine efficacy assessments will be performed upon completion of each cycle during treatment. PET-CT scanning will be used for efficacy evaluation after three cycles of therapy. Patients with stable disease (SD) or progressive disease (PD) will discontinue study treatment, and the investigator will determine the salvage therapy regimen. Patients achieving a complete response (CR) or partial response (PR) will continue the original regimen for cycles 4 to 6. After completion of six cycles of treatment, PET-CT will be conducted for efficacy reassessment. Patients with CR or PR will finish induction therapy and enter the maintenance phase. The study group will receive obinutuzumab maintenance therapy once every three months for a total of two years. |
环磷酰胺 IV 输注将按照各组指定的时间表进行。
多柔比星 IV 输注将按照各组指定的时间表进行。
泼尼松 PO 将按照各自手臂中指定的时间表进行管理。
Obinutuzumab IV infusion will be administered as per the schedule specified in the respective arm.
Vincristine infusion will be administered as per the schedule specified in the respective arm.
Bendamustine infusion will be administered as per the schedule specified in the respective arm.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Progression-free survival
大体时间:From enrollment to the first occurrence of disease progression or relapse, or death from any cause, whichever occurs earlier (a maximum of 6 years)
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PFS, defined as the time from diagnosis to the first occurrence of disease progression or relapse using the 2014 Lugano Response Criteria or death due to any cause, whichever occurs first; as determined by the investigator
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From enrollment to the first occurrence of disease progression or relapse, or death from any cause, whichever occurs earlier (a maximum of 6 years)
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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完全回复率
大体时间:治疗结束访视(第 6 周期第 1 天最后一次给药后 6-8 周 [周期长度 = 21 天]
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FDG-PET 治疗结束时的 CR 率定义为根据 2014 年卢加诺反应标准,治疗结束时达到 CR 的参与者比例;由研究者和 IRC(分别)确定
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治疗结束访视(第 6 周期第 1 天最后一次给药后 6-8 周 [周期长度 = 21 天]
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Objective response rate
大体时间:End of treatment visit (6-8 weeks after last dose on Day 1 of Cycle 6 [Cycle length=21 days]
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ORR at treatment completion or discontinuation defined as the proportion of participants with CR or partial response (PR) at the end of treatment according to the 2014 Lugano Response Criteria; as determined by the investigator and IRC(separately)
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End of treatment visit (6-8 weeks after last dose on Day 1 of Cycle 6 [Cycle length=21 days]
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Overall survival
大体时间:up to approximately 6 years
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OS defined as the time from diagnosis to death from any cause
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up to approximately 6 years
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Number of Participants With Treatment-Related Adverse Events as Assessed by CTCAE v6.0
大体时间:From enrollment to study completion, a maximum of 6 years
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Number of Participants With Treatment-Related Adverse Events as Assessed by CTCAE v6.0
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From enrollment to study completion, a maximum of 6 years
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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
关键字
其他相关的 MeSH 术语
- 肿瘤
- 免疫系统疾病
- 组织学类型的肿瘤
- 淋巴系统疾病
- 淋巴增生性疾病
- 免疫增生性疾病
- 淋巴瘤,非霍奇金
- 淋巴瘤
- 半身和淋巴疾病
- 淋巴瘤,滤泡性
- 有机化学品
- 杂环化合物,1形
- 杂环化合物
- 苯甲酰唑
- 杂环化合物,2环
- 杂环化合物,融合环
- 碳氢化合物
- 碳氢化合物,循环
- 碳水化合物
- 酸,无环
- 羧酸
- 生物碱
- 多环芳烃
- 碳氢化合物,芳香族
- 多环化合物
- 糖苷
- 哌啶
- 吲哚
- 怀孕
- 怀孕
- 类固醇
- 融合环化合物
- 磷酰胺芥末
- 氮芥末化合物
- 芥末化合物
- 碳氢化合物,卤素
- 磷酰胺
- 有机磷化合物
- 妊娠二培养子
- VINCA生物碱
- Secologanin色素生物碱
- 吲哚生物碱
- 吲哚衍生物
- 吲哚王
- 蒽环类动物
- 萘烯
- 氨基糖苷
- 丁酸酯
- Daunorubicin
- 邻苯二甲胺
- 邻苯二甲酸
- 酸,碳环
- 哌啶酮
- 等词
- 来那度胺
- 盐酸苯达莫司汀
- 强的松
- 环磷酰胺
- 阿霉素
- 长春新碱
- obinutuzumab
- Olelabrutinib
其他研究编号
- Future
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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