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

NCT ID: NCT03130582

Last Updated: 2017-04-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

88 participants

Study Classification

OBSERVATIONAL

Study Start Date

2005-11-30

Study Completion Date

2016-12-31

Brief Summary

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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

Detailed Description

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Conditions

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Lymphoma

Keywords

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high-dose etoposide,autologous peripheral blood stem cell transplantation

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Disease status at mobilization PR

high-dose etoposide

Intervention Type DRUG

an epipodophyllotoxin, is one of the most common chemotherapy agents for lymphoma without reciprocal resistance with other kinds of agents.

Disease status at mobilization PD

high-dose etoposide

Intervention Type DRUG

an epipodophyllotoxin, is one of the most common chemotherapy agents for lymphoma without reciprocal resistance with other kinds of agents.

Interventions

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high-dose etoposide

an epipodophyllotoxin, is one of the most common chemotherapy agents for lymphoma without reciprocal resistance with other kinds of agents.

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* relapsed/refractory lymphoma ,siut APBSCT

Exclusion Criteria

* bone marrow without involvement by lymphoma cells
Minimum Eligible Age

16 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Yang Jun

OTHER

Sponsor Role lead

Responsible Party

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Yang Jun

Principal Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Other Identifiers

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2015KY143

Identifier Type: -

Identifier Source: org_study_id