Chemotherapy-induced Thrombocytopenia in Patients With Lymphoma and lung cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Male or female patients at the age of 18 to 75 years old; 2) Histologically or cytologically diagnosed Lymphoma and lung cancer cases; 3) Platele counts is less than or equal to 75*10^9/L during screening chemotherapy cycle, or appears the risk of clinically significant CIT: previous bleeding episodes in last 3 months; baseline platelets less than 75*10^9/L; those patients receiving platinumbased, Cytarabine, anthracycline-based, gemcitabine-based regimen; bone marrow metastases; ECOG PS >=2; received prior radiotherapy (Especially the long bones, flat bones); 4) With understanding ability and voluntarily sign informed consent form; 5) Be able to comply with the study and follow-up process.
Exclusion criteria
Exclusion criteria: 1) Breast-feeding or pregnant women; 2) Platelet count over 400*10^9/L; 3) patients who had severe allergic history on biological preparation; 4) Septicemia, Disseminated intravascular coagulation (DIC), Hypersplenism, ITP, Stem cell transplantation, Leukemia, Bone marrow dysplasia or any other illness sickness that can exacerbate thrombocytopenia appeared in the previous cycles of chemotherapy; 5) The investigator think that the child should not participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| blood routine examination; | — |
Countries
China