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Efficacy of prophylactic TPO on TCP reduction in high-intensity chemotherapy of malignant ymphoma

Efficacy of prophylactic TPO on TCP reduction in high-intensity chemotherapy of malignant ymphoma

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018737
Enrollment
Unknown
Registered
2018-10-07
Start date
2018-10-15
Completion date
Unknown
Last updated
2018-10-10

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

Conditions

lymphoma

Interventions

A:rhTPO 15000U injectioninjection at Day -2\-1\and day 2-7, total 8 doses.
B:rhTPO 15000U injection everyday for 8 doses after chemotherapy

Sponsors

Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients with lymphoma confirmed by histopathology and who was relapsed or progress after first-line treatment; 2. Aged 18 to 65 years; 3. ECOG performance status of 0,1or2; 4. At least one measurable lesion is present; 5. Life expectancy of >3 months; 6. Adequate hepatic function: ALT =3G/L, absolute neutrophil count >=1.5G/L, hemoglobin>=100g/L, and platelet count >=75G/L; 7. LVEF>=45% by echocardiography; 8. Cardiac function was classified as grade I, II; 9. Signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Lymphoma invades the central nervous system; 2. History of severe allergic or anaphylactic reactions to any drugs including the protocol; 3. Evidence of significant, uncontrolled concomitant diseases that could affect compliance with the protocol or interpretation of results, including significant cardiovascular disease, uncontrolled diabetes mellitus, pulmonary disease or severe hepatic and renal dysfunction; 4. serious infections; 5. History of other malignancy; 6. Mental disorder; 7. All patients of reproductive potential refuse to use adequate methods of contraception during the treatment period; 8. Patients were not suitable for this study concluded by researchers.

Design outcomes

Primary

MeasureTime frame
Platelet minimum;

Secondary

MeasureTime frame
Thrombocytopenia duration;Platelet transfusion volume;incidence of level III thrombocytopenia;incidence of level IV thrombocytopenia;Cost associated with thrombocytopenia;

Countries

China

Contacts

Public ContactLiling Zhang

Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

xhzlwg@163.com+86 15871725926

Outcome results

None listed

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