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High-dose Etoposide Could Discriminate Patients With Refractory/Relapsed Lymphoma Benefit From APBSCT

Y

Yang Jun

Status

Completed

Conditions

Lymphoma

Treatments

Drug: high-dose etoposide

Study type

Observational

Funder types

Other

Identifiers

NCT03130582
2015KY143

Details and patient eligibility

About

patients with refractory /relapsed lymphoma received high-dose etoposide for hematopoietic stem cell (HSC) mobilization.All patients received high-dose etoposide 20-25 mg/kg/d intravenously for two consecutive days followed by rhG-CSF10ug/kg/day subcutaneously at 48 hours after chemotherapy; rhG-CSF was continued until the end of harvesting for HSCs/HPCs. Peripheral blood counts were performed daily for all patients following the initiating of rhG-CSF. Leukapheresis was performed when peripheral blood white blood count exceeded 4×109/L with blood cell The harvested cells reached at least 2*108/kg for mononuclear cells and/or 2*106/kg for CD34+ cells with once to twice leukapheresis. The final product was kept frozen in liquid nitrogen.Auto-PBSCT

Enrollment

88 patients

Sex

All

Ages

16 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • relapsed/refractory lymphoma ,siut APBSCT

Exclusion criteria

  • bone marrow without involvement by lymphoma cells

Trial design

88 participants in 2 patient groups

Disease status at mobilization PR
Treatment:
Drug: high-dose etoposide
Disease status at mobilization PD
Treatment:
Drug: high-dose etoposide

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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