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Study of PD-1 Antibody and Bevacizumab in the Treatment of High-risk GTN After Combined Chemotherapy

Phase II Single-arm Clinical Study of PD-1 Antibody and Bevacizumab in the Treatment of Relapsed or Refractory High-risk Gestational Trophoblasitc Neoplasia After Second-line or Above Combined Chemotherapy

Gestational trophoblastic Neoplasia(GTN) is a kind of malignant tumor in women of childbearing age. It is easy to metastasized through the blood system in the early stage, so it is a relatively malignant tumor. The tumor is highly sensitive to chemotherapy, and low-risk patients have good prognosis, with survival rate and cure rate approaching 100%, but high-risk patients are prone to drug resistance, or relapse after remission. For relapsed, refractory, high-risk GTN, multiple remedies have been reported in the literature, but the remission rate is only 75-80%. For relapsed or refractory high-risk GTN, multiple remedies have been reported in the literature, but the remission rate is only 75-80%.

Currently, targeted therapy and immunotherapy are widely used in various refractory solid tumors. For GTN, there are also a number of related studies. In this study, PD-1 inhibitors combined with bevacizumab were used to treat refractory high-risk GTN with relapse or drug resistance after receiving previous second-line or above multidrug combination therapy, to study the efficacy and safety of the treatment regimen.

研究概览

详细说明

In this study, PD-1 inhibitors combined with bevacizumab were used to treat refractory high-risk trophoblastic tumor (GTN) with relapse or drug resistance after receiving previous two-line or above multidrug combination therapy, and the efficacy and safety of the two drugs were evaluated.

Patients who meet the requirements will sign the informed consent and be enrolled voluntarily. This project is a single-arm study without a control group. Twenty patients are expected to be enrolled, and there are 4 centers competing for enrollment.

All patients received at least two-line multidrug combination therapy, and some patients may have undergone or planned surgery and/or radiation therapy. Through the HCG value and measurable changes in the size of the lesions, we can understand the changes of the disease. The primary endpoints were PFS and ORR Whenever, for whatever reason, the subject does not complete the clinical trial observation, is considered to be an abscission case. When the subject falls off, the researcher must fill in the reason for the fall off in the CRF, and contact the subject as much as possible, complete the items that can be evaluated, and record the time of the last medication to prepare for the analysis of its efficacy and safety. The CRF should be kept for future reference

研究类型

介入性

注册 (预期的)

20

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:Xing Xie, phD
  • 电话号码:+8613606705128
  • 邮箱:panzimin@163.com

研究联系人备份

学习地点

    • Zhejiang
      • Hangzhou、Zhejiang、中国、310000
        • 招聘中
        • Women's Hospital School Of Medicine Zhejiang University
        • 接触:
          • Xing Xie, phD

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

18年 至 75年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

女性

描述

Inclusion Criteria:

  1. Signed Informed Consent
  2. Clinically diagnosed as recurrent or drug-resistant trophoblastic tumor
  3. After treatment with at least two or more multidrug chemotherapy regimens
  4. Survival is expected to exceed 3 months
  5. Age ≥18 years, age ≤75 years
  6. Karnofsky score ≥60分,ECOG score ≤2分
  7. No serious complications
  8. Take effective contraceptives during treatment
  9. Patients can be followed up as required
  10. Blood test within 3 days: ANC≥1.5×109/L, PT ≥100×109/L, Hb≥90g/L, BIL ≤ 1.5 times of the high limit of normal value, ALT/ALST ≤ 1.5 times of the high limit of normal value, BUN and Cr≤ normal value
  11. Coagulation function, thyroid function and myocardial enzyme in the normal range

Exclusion Criteria:

  1. Previously, he had received anti-PD-1, anti-PD-L1, bevacizumab and other drugs;
  2. Within 2 weeks before the first administration, he had received anticancer Chinese patent medicine or immunomodulatory drugs;
  3. Within 2 years before the first administration, he had received active autoimmune disease requiring systemic treatment;
  4. Were receiving systemic glucocorticoid therapy or any other form of immunosuppressive therapy within 7 days prior to first administration;
  5. Clinically uncontrollable pleural effusion/peritoneal effusion is present;
  6. Allergic to PD-1 monoantibody, bevacizumab and other active ingredients or excipients;
  7. Failure to fully recover from toxicity and/or complications;
  8. History of HIV infection, untreated active hepatitis B, and active HCV infection subjects;
  9. Live vaccine was administered within 30 days prior to the first dose;
  10. Patients with serious or uncontrollable medical conditions who are not suitable for chemotherapy;
  11. Participating in clinical trials of other drugs at the same time or 4 weeks before the first administration。

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
实验性的:Double medicine combined
participants received 200mg of PD-1 inhibitors combined 15mg of bevacizumab per square body surface area intravenously every 3 weeks
Both drugs are given intravenously
其他名称:
  • 注射用卡瑞利珠单抗

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
PFS
大体时间:From date of randomization until the date of first documented progression or death from any cause, whichever occurred first, or last follow-up for patients alive without progression, assessed up to approximately 24 months
PFS is defined as the time from randomization to the first occurrence of PD, as determined by the investigator using RECIST v1.1, or death from any cause during the study, whichever occurs first.
From date of randomization until the date of first documented progression or death from any cause, whichever occurred first, or last follow-up for patients alive without progression, assessed up to approximately 24 months

次要结果测量

结果测量
措施说明
大体时间
ORR
大体时间:From date of randomization until PD or death from any cause, assessed up to 24 months
ORR is defined as the rate of CR or PR.Partial response (PR) is defined as a reduction of HCG by 50% or more from the starting value in continuous measurements; Complete response (CR) is defined as HCG normalization of continuous measurements at least two weeks intervals.
From date of randomization until PD or death from any cause, assessed up to 24 months

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。

调查人员

  • 首席研究员:Xing Xie, doctor、Women's Hospital School Of Medicine Zhejiang University

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

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 (实际的)

2021年4月15日

初级完成 (预期的)

2024年4月15日

研究完成 (预期的)

2026年4月15日

研究注册日期

首次提交

2021年3月21日

首先提交符合 QC 标准的

2021年3月22日

首次发布 (实际的)

2021年3月23日

研究记录更新

最后更新发布 (实际的)

2022年6月3日

上次提交的符合 QC 标准的更新

2022年6月2日

最后验证

2022年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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.

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