To evaluate the clinical application value in bone marrow protection of Trilaciclib in the neoadjuvant treatment of stage II/III classic osteosarcoma in combination with pirarubicin and lobaplatin.
Classic osteosarcoma is the most common primary bone malignancy. At present, osteosarcoma is usually treated with preoperative chemotherapy, surgical operation and postoperative chemotherapy. Treatment with preoperative chemotherapy is also known as neoadjuvant chemotherapy. Neoadjuvant chemotherapy has brought benefits to patients, but safety concerns are inevitable. Myelosuppression is a major factor affecting the compliance of patients treated by chemotherapy. Patients with chemotherapy-induced myelosuppression(CIM) have higher rates of infection, sepsis, bleeding, and fatigue, resulting in hospitalization, hematopoietic growth factor support, blood transfusions (red blood cells and/or platelets) and even death. In addition, CIM often leads to dose reduction and delayed administration, which limits the therapeutic dose intensity and therefore affects the anti-tumor efficacy of chemotherapy. Currently, there are no approved treatments in osteosarcoma to prevent chemotherapy-induced cell damage. Although some treatments may help to address CIM when it occurs such as blood transfusions and growth factors, these treatments are pedigree specific, being used after hematopoietic stem progenitor cells damage and could bring additional toxicity. Trilaciclib is a highly effective, selective and temporarily reversible inhibitor of CDK4/6. The proliferation of bone marrow hematopoietic stem cells depends on CDK4/6 activity. Bone marrow hematopoietic stem cells are blocked in the G1 phase of the cell cycle after exposure to Trilaciclib before chemotherapy is given. Therefore, this study is conducted to evaluate the clinical application value in bone marrow protection of Trilaciclib in the neoadjuvant treatment of stage II/III classic osteosarcoma in combination with pirarubicin and lobaplatin.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Enrollment
50
Trilaciclib: 240mg/m2, IV, within 4 hours before each chemotherapy agent infused.
Pirarubicin: 60 mg/m2,IV,d1-2
LobaplLatin: 40 mg/m2,,IV,d1
Peking University People's Hospital
Beijing, Beijing Municipality, China
RECRUITINGIncidence of grade 3/4 neutropenia
Incidence of grade 3/4 neutropenia up to 30 days
Time frame: up to 30 days
Duration of grade 3/4 neutropenia
Duration of grade 3/4 neutropenia up to 30 days
Time frame: up to 30 days
Incidence of grade 3/4 thrombocytopenia
Incidence of grade 3/4 thrombocytopenia up to 30 days
Time frame: up to 30 days
Incidence of grade 3 or 4 anemia
Incidence of grade 3 or 4 anemia up to 30 days
Time frame: up to 30 days
Incidence of febrile neutropenia
Incidence of febrile neutropenia up to 30 days
Time frame: up to 30 days
Usage of granulocyte colony-stimulating factor (G-CSF)
Utilization rate of granulocyte colony-stimulating factor (G-CSF) up to 30 days
Time frame: up to 30 days
Usage of Thrombopoietin (TPO)
Utilization rate of Thrombopoietin (TPO) up to 30 days
Time frame: up to 30 days
Usage of Erythropoietin (ESA)
Utilization rate of Erythropoietin (ESA) up to 30 days
Time frame: up to 30 days
Incidence of platelet transfusion
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Incidence of platelet transfusion up to 30 days
Time frame: up to 30 days
Incidence of red blood cell transfusion
Incidence of red blood cell transfusion up to 30 days
Time frame: up to 30 days
Usage of ferralia
Utilization rate of ferralia up to 30 days
Time frame: up to 30 days
chemotherapy dose reduction of any cause
chemotherapy dose reduction rate of any cause up to 30 days
Time frame: up to 30 days
AE adverse event adverse event adverse event
adverse event
Time frame: up to 30 days
SAE
serious adverse event serious adverse event serious adverse event Serious Adverse Event
Time frame: up to 30 days
Termination of treatment caused by AE/SAE
Termination of treatment rate caused by AE/SAE
Time frame: up to 30 days