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Study of Standard and Individualized Treatment Model for Relapse and Refractory Lymphatic System Malignant Tumors

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02929615
Enrollment
50
Registered
2016-10-11
Start date
2015-06-30
Completion date
2018-03-31
Last updated
2016-10-12

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

Conditions

Lymphoma

Brief summary

The purpose of the study is to research the standard and individualized treatment model for relapse and refractory lymphatic system malignant tumors.

Interventions

OTHERHematopoietic stem cell transplantation

Sponsors

Peking University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Patients with relapse and refractory lymphoma and multiple myeloma. 2. At least 1 measurable lesions and its size≥15mm. 3. Patients ≤65 years,no limitations for both gender. 4. ECOG score is 0-1. 5. Life expectancy≥3 months. 6. LVEF≥ 55%; Peripheral blood: WBC ≥ 3.5×10(9)/L,neutrophil ≥1.5×10(9)/L, PLT≥75×109/L,Hb≥90g/L; Renal function: Cr≤2.0×UNL; Liver function: BIL≤2.0×UNL,ALT/AST≤2.5×UNL; 7. Written informed consent are acquired.

Exclusion criteria

1. Previously received stem cell transplantation. 2. Women with pregnant, lactating or not to take contraceptive measures. 3. Severe acute infection or suppurative and chronic infection that wound not healing. 4. Severe heart failure. 5. Suffering from mental disorders and poor compliance. 6. Other situations that investigators consider as contra-indication for this study.

Design outcomes

Primary

MeasureTime frame
overall response rate2 years after treatment
complete response2 years after treatment
progression-free survival2 years after treatment
overall survival2 years after treatment

Countries

China

Contacts

Primary ContactZhu Jun, archiater
Zhujun@csco.org010-88196596

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026