Skip to content

Prospective, Non-Interventional, Multi-Centre Trial of recombinant human thrombopoietin (rhTPO) in the Treatment of Chemotherapy-induced Thrombocytopenia in Patients With Lymphoma and lung cancer

Prospective, Non-Interventional, Multi-Centre Trial of recombinant human thrombopoietin (rhTPO) in the Treatment of Chemotherapy-induced Thrombocytopenia in Patients With Lymphoma and lung cancer

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-15006803
Enrollment
Unknown
Registered
2015-07-24
Start date
2015-07-21
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chemotherapy-induced Thrombocytopenia in Patients With Lymphoma and lung cancer

Interventions

rhTPO:Patients will receive 3 periods equally chemotherapy, It is clear to assess the dose and schedule of treatment with rhTPO from Package insert and Expert consensus on diagnosis and treatment of

Sponsors

Jiangsu Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

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

MeasureTime frame
blood routine examination;

Countries

China

Contacts

Public ContactJifeng Feng
fjif@medmail.com.cn+86 010 8489 2211

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026