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A Clinical Study on Prophylactic RespOnse To hEtrombopag for Secondary Prevention in Anti-Cancer Therapy-induced Thrombocytopeniae (PROTECT)

2026年6月9日 更新者:Jian Zhang,MD、Fudan University

This study is a prospective clinical study enrolling breast cancer patients at high risk of chemotherapy-induced thrombocytopenia (CTIT). It aims to investigate the efficacy and safety of hetrombopag in the secondary prophylaxis of CTIT.

Breast cancer patients with histologically or cytologically confirmed disease were enrolled after signing the informed consent form and were randomly assigned in a 1:1:1 ratio to three Arms. Stratification factors for randomization included the number of prior antineoplastic treatment cycles (>2 cycles vs. ≤2 cycles).

Arm 1: No prophylactic use of hetrombopag Arm 2: Hetrombopag at an initial dose of 7.5 mg once daily, administered from Day 1 of the first chemotherapy cycle (C1D1) continuously until the end of the second chemotherapy cycle Arm 3: Hetrombopag at an initial dose of 7.5 mg once daily, administered from Day 1 (C1D1) to Day 14 (C1D14) of the first chemotherapy cycle; the dosage and administration schedule in the second chemotherapy cycle were identical to those in the first cycle; Treatment continued until patients completed the protocol-specified treatment and follow-up, experienced intolerable toxicity, withdrew informed consent, initiated alternative antitumor therapy, died, or met any other treatment discontinuation criteria specified in the protocol, whichever occurred first.

研究概览

研究类型

介入性

注册 (估计的)

126

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

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:

  1. Age ≥ 18 years;
  2. Patients with histopathologically confirmed breast cancer;
  3. Receiving or expected to receive chemotherapy-based antitumor therapy with a cycle length of ≥21 days, and anticipated to receive ≥2 cycles of therapy;
  4. ECOG performance status 0-2;
  5. Platelet count meeting **one** of the following criteria:

    1. Nadir platelet count < 50×10⁹/L in the previous antitumor treatment cycle;
    2. Nadir platelet count ≥ 50×10⁹/L but < 75×10⁹/L in the previous antitumor treatment cycle, accompanied by **high risk factors for bleeding***;
  6. Platelet count ≥ 100×10⁹/L at enrollment;
  7. Patients with breast cancer plus other malignancies are allowed, provided that the treatment plan is primarily for breast cancer;
  8. Adequate organ function:

    • Bone marrow: ANC ≥ 1.5×10⁹/L; hemoglobin ≥ 8 g/dL;

      • Hepatic and renal function: total bilirubin ≤ 1.5 × ULN; ALT, AST ≤ 2.5 × ULN (or ≤ 5 × ULN in the presence of liver metastasis); serum creatinine ≤ 1.5 × ULN or creatinine clearance > 60 mL/min (Cockcroft-Gault formula);

        • Coagulation: activated partial thromboplastin time (APTT) and international normalized ratio (INR) ≤ 1.5 × ULN;
  9. Female subjects of childbearing potential must have a negative serum pregnancy test within 7 days prior to the first dose, not be breastfeeding, and agree to use effective contraception during the study and for 7 days after the last dose of study drug.

    Male subjects with female partners of childbearing potential must be surgically sterile or agree to use effective contraception during the study and for 7 days after the last dose of study drug; sperm donation is prohibited during the study;

  10. Life expectancy ≥ 3 months;
  11. Voluntarily participate in the study, sign the informed consent form, have good compliance, and be willing to comply with follow-up procedures.

    • High risk factors for bleeding History of bleeding; prior treatment with platinum agents, gemcitabine, cytarabine, anthracyclines, PARP inhibitors (e.g., niraparib), etc.; combination of targeted agents and chemotherapeutic agents known to increase the risk of thrombocytopenia; history of radiotherapy or ongoing radiotherapy, especially to long bones and flat bones (e.g., pelvis, sternum).

Exclusion Criteria:

  1. Presence of hematological disorders, including but not limited to leukemia, primary immune thrombocytopenia, myeloproliferative neoplasms, multiple myeloma, and myelodysplastic syndromes;
  2. Uncontrolled active infection;
  3. History of arterial or venous thrombosis;
  4. Patients with bleeding tendency, or evidence of inherited bleeding diathesis or coagulation disorders;
  5. Pregnant or breastfeeding women, or female patients of childbearing potential not using effective contraception;
  6. Participation in another clinical trial of thrombopoietic agents within 4 weeks prior to enrollment;
  7. Presence of uncontrolled neurological or psychiatric disorders, poor compliance, or inability to cooperate and report treatment-related reactions;
  8. Bone marrow involvement;
  9. Administration of rhTPO or rhIL-11 within 7 days prior to enrollment;
  10. Hypersensitivity to the study drug(s).

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: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
无干预:No prophylactic use of hetrombopag
实验性的:Continuous Hetrombopag for 2 Cycles
Hetrombopag at an initial dose of 7.5 mg once daily, administered from Day 1 of the first chemotherapy cycle (C1D1) continuously until the end of the second chemotherapy cycle
Hetrombopag at an initial dose of 7.5 mg once daily, administered from Day 1 of the first chemotherapy cycle (C1D1) continuously until the end of the second chemotherapy cycle
实验性的:Cyclic 14-day Hetrombopag for 2 Cycles
Hetrombopag at an initial dose of 7.5 mg once daily, administered from Day 1 (C1D1) to Day 14 (C1D14) of the first chemotherapy cycle; the dosage and administration schedule in the second chemotherapy cycle were identical to those in the first cycle
Hetrombopag at an initial dose of 7.5 mg once daily, administered from Day 1 (C1D1) to Day 14 (C1D14) of the first chemotherapy cycle

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Incidence of grade ≥2 thrombocytopenia (PLT < 75×10⁹/L)
大体时间:At the end of Cycle 2 (each cycle ≥21 days)
At the end of Cycle 2 (each cycle ≥21 days)

次要结果测量

结果测量
大体时间
Duration of grade ≥2 thrombocytopenia (PLT < 75×10⁹/L)
大体时间:At the end of Cycle 2 (each cycle ≥21 days)
At the end of Cycle 2 (each cycle ≥21 days)
Incidence and duration of grade ≥3 thrombocytopenia (PLT < 50×10⁹/L)
大体时间:At the end of Cycle 2 (each cycle ≥21 days)
At the end of Cycle 2 (each cycle ≥21 days)
Proportion of patients who successfully completed two chemotherapy cycles without thrombocytopenia-related modifications to subsequent antineoplastic therapy
大体时间:At the end of Cycle 2 (each cycle ≥21 days)
At the end of Cycle 2 (each cycle ≥21 days)
Proportion of patients without rescue therapy for thrombocytopenia (e.g., platelet transfusion, interleukin-11, recombinant human thrombopoietin)
大体时间:At the end of Cycle 2 (each cycle ≥21 days)
At the end of Cycle 2 (each cycle ≥21 days)
Nadir and peak platelet counts
大体时间:At the end of Cycle 2 (each cycle ≥21 days)
At the end of Cycle 2 (each cycle ≥21 days)
Incidence of adverse events
大体时间:From enrollment to 21 days after the last dose of study drug
From enrollment to 21 days after the last dose of study drug

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。

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 (估计的)

2026年5月28日

初级完成 (估计的)

2028年2月29日

研究完成 (估计的)

2028年3月31日

研究注册日期

首次提交

2026年5月23日

首先提交符合 QC 标准的

2026年6月9日

首次发布 (实际的)

2026年6月15日

研究记录更新

最后更新发布 (实际的)

2026年6月15日

上次提交的符合 QC 标准的更新

2026年6月9日

最后验证

2026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

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