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Trial of Surufatinib Combined With Toripalimab in the Treatment of Peritoneal Metastatic Carcinoma of Gastrointestinal or Primary Peritoneal Cancer

2021年8月27日 更新者:Shen Lin、Peking University

A Phase Ⅱ, Single-arm Study to Evaluate the Efficacy and Safety of Surufatinib Combined With Toripalimab in Peritoneal Metastatic Carcinoma of Gastrointestinal or Primary Peritoneal Cancer

This is a phase II, single arm, open-label, single-center study to evaluate the efficacy and safety of Surufatinib combined with Toripalimab in patients with peritoneal metastatic carcinoma of gastrointestinal or primary peritoneal cancer.

研究概览

详细说明

The study population is about 72 patients with advanced peritoneal metastatic carcinoma of gastrointestinal or primary peritoneal cancer, who fails or cannot tolerate standard therapies. Surufatinib 250 mg once a day (QD) will be orally administrated and Toripalimab 240mg will be intravenously administered every 3 weeks up to documented disease progression, development of unacceptable toxicity, participant request, or withdrawal of consent. For Toripalimab, the upper time limit for treatment is 2 years. The primary objective is overall survival (OS) of Surufatinib combined with Toripalimab in patients with advanced solid advanced peritoneal metastatic carcinoma of gastrointestinal or primary peritoneal cancer.

研究类型

介入性

注册 (预期的)

72

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

学习地点

    • Beijing
      • Beijing、Beijing、中国、100142
        • 招聘中
        • Beijing Cancer Hospital
        • 接触:
          • Lin Shen, MD
          • 电话号码:86-10-88196561

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 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Histologically or cytologically confirmed advanced peritoneal metastatic carcinoma of gastrointestinal or primary peritoneal cancer
  2. Failed after standard treatment
  3. Have evaluable lesions, including those that are not measurable
  4. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1;
  5. Adequately understand the study and voluntarily sign the Informed Consent Form;
  6. ≥18 years old;
  7. Lab tests within 7 days before first dose:

1) Absolute neutrophil count (ANC) ≥1.5×109/L, platelet count ≥100×109/L, and hemoglobin ≥100g/L; 2) Serum total bilirubin ≤1.5 times the upper limit of normal (ULN); 3) Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels ≤2.5 times the ULN; 4) Patients without anticoagulant therapy: International Normalized Ratio (INR) ≤1.5 ULN and activated partial thromboplastin time (APTT) ≤1.5 ULN. If patients received anticoagulant therapy: INR ≤2 ULN and APTT was within the normal range 14 days before treatment; 5) Serum total bilirubin <1.5 times the upper limit of normal (ULN); 6) Urine protein < 2+; if ≥2+, 24-hour urine protein <1 g; 8. Male or females patients with reproductive potential must agree to use an effective contraceptive method, for example, double-barrier device, condom, oral or injected birth control medication or intrauterine device, during the study and within 90 days after study treatment discontinuation. All female patients are considered to be fertile, unless the patient had natural menopause or artificial menopause or sterilization (such as hysterectomy, bilateral oophorectomy or ovarian irradiation).

Exclusion Criteria:

  1. Prior system treatment with antiPD1/PDL1/PDL2/CTLA-4 antibody or Sulfatinib;
  2. Previous intraperitoneal treatment with immunologic agents;
  3. Patients with digestive tract obstruction or uncontrolled active bleeding from the primary tumor;
  4. Patients with any active autoimmune disease or a documented history of autoimmune disease: Patients with hypothyroidism but receiving a stable dose of thyroid hormone replacement therapy were included in the study, and subjects with stable type 1 diabetes were able to control their blood sugar;
  5. Pulmonary fibrosis, interstitial pneumonia, pneumoconiosis, radiation pneumonitis, drug-associated pneumonia, severe impaired lung function, etc;
  6. Prior major surgery within past 4 weeks and had not fully recovered from previous surgery;
  7. Active bleeding or abnormal coagulation, Prone to bleeding or receiving thrombolytic or anticoagulant therapy;
  8. Hypertension that is not controlled by the drug, and is defined as: SBP≥140 mmHg and/or DBP≥90 mmHg;
  9. Prior antitumor therapy (including chemotherapy, immunotherapy, biological treatment, Targeted therapy, etc) , or have not recovered from toxicities since the last treatment;
  10. Pregnant or nursing;
  11. previously received allogeneic stem cell or parenchymal organ transplantation;
  12. Any significant clinical or laboratory abnormality that the investigator considers to influence the safety evaluators;
  13. History of uncorrected serum electrolyte disturbances such as potassium, calcium, or magnesium;
  14. Known human immunodeficiency virus (HIV) infection;
  15. Active hepatitis B virus (HBV) and hepatitis C virus (HCV) infected persons;
  16. A history of other malignancies within 5 years prior to inclusion, except for cervical carcinoma in situ, basal or squamous cell skin cancer, localized prostate cancer treated with radical surgery, and ductal carcinoma in situ treated with radical surgery;
  17. Prior treatment with corticosteroids (dose > 10 mg/day prednisone or other hormones) or other immunosuppressive agents within 2 weeks, nasal or inhalation in allowed (dose > 10 mg/day prednisone or other hormones);
  18. Severe, uncontrolled medical condition that would affect patients' compliance or obscure the interpretation of toxicity determination or adverse events, including active severe infection, uncontrolled diabetes, angiocardiopathy (heart failure > class II NYHA, LVEF <50%, myocardial infarction, unstable arrhythmia or unstable angina within past 6 months, cerebral infarction within past 3 months) or pulmonary disease ( interstitial pneumonia, obstructive pulmonary disease or symptomatic bronchospasm);
  19. History with tuberculosis who are receiving or have received anti-TB treatment within 1 year;
  20. Active infection;
  21. Receiving another experimental drug or participating in a clinical study for another therapeutic purpose within the first 28 days prior to treatment initiation;
  22. Any other disease, metabolic disorder, abnormal results of a physical examination or laboratory examination, and reasonably suspected disease or condition that may contraindication the use of the investigational drug, or affect the reliability of the study results, or place the patient at high risk for treatment complications, or affect patient compliance.

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:Surufatinib 250mg/Toripalimab 240mg
Surufatinib at a dose of 250mg Qd, with humanized anti-PD-1 monoclonal antibody(Toripalimab) injected intravenously 240mg per 3 weeks until disease progresses or unacceptable tolerability occurs.
Surufatinib 250mg will be taken orally once daily continuously through a 21-day cycle of study treatment. Toripalimab 240mg will be intravenously administered on Day 1 of each cycle.
其他名称:
  • HMPL-012/JS001

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
Overall Survival (OS)
大体时间:From date of first dose of study drug until withdrawal of consent or death (up to approximately 1 year)
Duration from the date of initial treatment with Surufatinib plus toripalimab to the date of death due to any cause.
From date of first dose of study drug until withdrawal of consent or death (up to approximately 1 year)

次要结果测量

结果测量
措施说明
大体时间
Progression-free Survival (PFS)
大体时间:From date of first dose of study drug until disease progression, withdrawal of consent, death, new anti-cancer therapy (up to approximately 1 year)
A duration from the date of initial treatment with Surufatinib combined with Toripalimab to disease progression or death of any cause.
From date of first dose of study drug until disease progression, withdrawal of consent, death, new anti-cancer therapy (up to approximately 1 year)
adverse events
大体时间:1 year
Adverse events assessments are computed and categorized according to the Common Toxicity Criteria of the National Cancer Institute, version 5.0
1 year

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 (实际的)

2021年7月14日

初级完成 (预期的)

2023年4月30日

研究完成 (预期的)

2023年7月30日

研究注册日期

首次提交

2021年8月24日

首先提交符合 QC 标准的

2021年8月27日

首次发布 (实际的)

2021年9月1日

研究记录更新

最后更新发布 (实际的)

2021年9月1日

上次提交的符合 QC 标准的更新

2021年8月27日

最后验证

2021年7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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