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

9 de junio de 2026 actualizado por: 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.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Estimado)

126

Fase

  • Fase 2

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Jian Zhang
  • Número de teléfono: +8618017312991
  • Correo electrónico: syner2000@163.com

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

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).

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Sin intervención: No prophylactic use of hetrombopag
Experimental: 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
Experimental: 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

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Incidence of grade ≥2 thrombocytopenia (PLT < 75×10⁹/L)
Periodo de tiempo: At the end of Cycle 2 (each cycle ≥21 days)
At the end of Cycle 2 (each cycle ≥21 days)

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Duration of grade ≥2 thrombocytopenia (PLT < 75×10⁹/L)
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: At the end of Cycle 2 (each cycle ≥21 days)
At the end of Cycle 2 (each cycle ≥21 days)
Incidence of adverse events
Periodo de tiempo: From enrollment to 21 days after the last dose of study drug
From enrollment to 21 days after the last dose of study drug

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

28 de mayo de 2026

Finalización primaria (Estimado)

29 de febrero de 2028

Finalización del estudio (Estimado)

31 de marzo de 2028

Fechas de registro del estudio

Enviado por primera vez

23 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

9 de junio de 2026

Publicado por primera vez (Actual)

15 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

15 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

9 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

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