Bone marrow suppression after chemoradiotherapy
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Voluntary participation and written informed consent; 2. Age 18-80 years, regardless of gender; 3. Patients with a confirmed diagnosis of malignant tumor by histopathology or cytology; 4. Normal blood count, liver and kidney function, and electrocardiogram before radiotherapy/chemotherapy, with no symptoms of infection or fever; 5. Patients with indications for radiotherapy/chemotherapy and intended treatment; 6. Patients with no major organ damage and an estimated survival time of more than 3 months; 7. Patients with a KPS score = 70.
Exclusion criteria
Exclusion criteria: 1. Patients with underlying lung inflammation, or serious heart, liver, or kidney diseases, or those with severe infections; 2. Patients with mental illness or a history of severe mental illness; 3. Patients with myelodysplastic syndrome or primary hematologic disease; 4. Patients who have previously received other treatments similar to those in this study that may affect the observed outcomes; 5. Pregnant or breastfeeding women, or women who refuse contraception during the treatment observation period; 6. Patients with a history of severe allergies or specific physical conditions; 7. Patients with drug abuse or alcohol addiction; 8. Patients currently participating in other clinical trials; 9. Patients with allergies to the main ingredients of the investigational drug.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood Routine; | — |
Secondary
| Measure | Time frame |
|---|---|
| Erythropoietin;Thrombopoietin;Granulocyte colony-stimulating factor; | — |
Countries
China
Contacts
Gansu Provincial Hospital of Traditional Chinese Medicine