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Gemcitabine, Nab-paclitaxel, and Dexamethasone in Patients With Recurrent/refractory peripheral T cell lymphoma

Gemcitabine, Nab-paclitaxel, and Dexamethasone in Patients With Recurrent/refractory peripheral T cell lymphoma

Status
Recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800018710
Enrollment
Unknown
Registered
2018-10-04
Start date
2018-10-01
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

peripheral T cell lymphoma

Interventions

Case series:Receive Gemcitabine, Nab-paclitaxel, and Dexamethasone(GAD) chemotherapy

Sponsors

Sun Yat-sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Signed informed consen; aged 18-75 years; ECOG=0-2;pathological findings were peripheral T cell lymphoma; received chemotherapy or radiation with more than one regimen (anthracycline included), disease progression occurs at the end of chemotherapy (radiation) or during chemotherapy (radiation); There are measurable or/and evaluable lymphoma lesions; No serious organ dysfunction; Compliance with research and visit plans and other programme requirements; women of childbearing age with a negative pregnancy test.

Exclusion criteria

Exclusion criteria: Transformed lymphoma; Participated in other clinical trials in the last 3 months; There is a history of other malignancies secondary to lymphoma, or secondary lymphoma after chemotherapy or radiotherapy,or central invasion of lymphoma; Abnormal laboratory tests: ANC3ULN,Cr>2ULN;active infections, decompensated heart failure, dilated cardiomyopathy that require systemic antibiotic or antiviral therapy, coronary heart disease with depressed ST segment and myocardial infarction, severe organic disease and severe mental disease that have occurred in the last 6 months; Pregnant and lactating women;Treatment for lymphoma was performed within 30 days before enrollment.

Design outcomes

Primary

MeasureTime frame
objective response rate;

Secondary

MeasureTime frame
complete response rate;progression-free survival;overall survival;safety;

Countries

China

Contacts

Public ContactTongyu LIN

Sun Yat-sen University Cancer Center

tongyulin@hotmail.com+86 13926400320

Outcome results

None listed

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