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Effects of Gemcitabine, oxaliplatin and dexamethasone (GOD) as salvage treatment for elderly patients with refractory and relapsed peripheral T-cell lymphoma

Effects of Gemcitabine, oxaliplatin and dexamethasone (GOD) as salvage treatment for elderly patients with refractory and relapsed peripheral T-cell lymphoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-12002258
Enrollment
Unknown
Registered
2012-06-07
Start date
2004-04-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

relapsed or refractory peripheral T-cell lymphoma

Interventions

elderly patients with relapsed or refractory perip:Treated with Gemcitabine, oxaliplatin and dexamethasone (GOD) regimen

Sponsors

Shanghai Ninth People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. age >= 60 years and unsuitable for high dose therapy; 2. histologically confirmed diagnosis of peripheral T-cell lymphoma; 3. relapsed or refractory disease; 4. Eastern Cooperative Oncology Group performance status (ECOG PS) 0-2, expected life time >= 3 months; 5. signed informed consent.

Exclusion criteria

Exclusion criteria: 1. liver dysfunction:serum transaminases or bilirubin >= 2 times upper limit of normal value; 2. renal impairment: serum creatinine clearance <30 ml/min; 3. heart failure: left ventricular ejection fraction <0.45; 4. bone marrow suppression :absolute neutrophil count (ANC) <=1000/ul, hemoglobin level <=10 g/dl and platelets <=100000/ul; 5. uncontrolled infection; 6. positive human immunodeficiency virus tests.

Design outcomes

Primary

MeasureTime frame
response rate;toxicity evaluation;

Secondary

MeasureTime frame
overall survival;event-free survival;

Countries

China

Contacts

Public ContactZhu Qi
zhuqi70@hotmail.com+86 13764188348

Outcome results

None listed

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