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Clinical study on maintain treatment of chidamide in peripheral T cell lymphoma after autologous peripheral hematopoietic stem cell transplantation

Clinical study on maintain treatment of chidamide in peripheral T cell lymphoma after autologous peripheral hematopoietic stem cell transplantation: a randomized, single center, single arm, open study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800014269
Enrollment
Unknown
Registered
2018-01-02
Start date
2018-01-01
Completion date
Unknown
Last updated
2018-01-08

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:maintain treatment of chidamide

Sponsors

Department of Hematology, Xinqiao Hospital, Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Newly diagnosed peripheral T-cell lymphomas(PTCL), except ALK+ anaplastic large cell lymphoma(ALK+ALCL);The patients achieved = partial remission(PR) after 6 cycles of ECHOP, and then received autologous peripheral blood stem cell transplantation(APBSCT); Hematopoietic reconstitution is stable and the primary disease is stable,30-45d after APBSCT. And meet the following criteria: 1.Aged60, Estimated lifetime>3 months 2.No sever organ dysfunction (1) Cr55%; (4) Hb>9g/dL, Bilirubin<2.0mg/dl; 3. Voluntary participants, informed consent.

Exclusion criteria

Exclusion criteria: 1. Severe cardiac, renal or hepatic dysfunction; 2. Patients have other malignant cancer and must receive treatment; 3. Patients cant understand or follow study protocol due to clinical symptoms of brain dysfunction or serious mental illness; 4. Patients cant guarantee to accomplish treatment plan and follow-up; 5. Patients with severe acute hypersensitive reaction; 6. Uncontrolled active infection; 7. Patients who have been enrolled in other clinical trial; 8. Patients arent suitable for this clinical trial according to investigators judgement.

Design outcomes

Primary

MeasureTime frame
recurrence rate;

Secondary

MeasureTime frame
leukopenia;anemia;thrombocytopenia;gastrointestinal reaction;liver damage;renal damage;

Countries

China

Contacts

Public ContactXi Zhang

Department of Hematology, Xinqiao Hospital, Third Military Medical University

zhangxxi@sina.com+86 13808310064

Outcome results

None listed

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