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The efficientcy of thalidomide plus cyclophosphamide and dexamethasone following by thalidomide and prednisone maintaince therapy for the newly diagnosed Waldenstr?m macroglobulinemia - a Prospective Multicentre Phase III Trial from China

The efficientcy of thalidomide plus cyclophosphamide and dexamethasone following by thalidomide and prednisone maintaince therapy for the newly diagnosed Waldenstr?m macroglobulinemia - a Prospective Multicentre Phase III Trial from China

Status
Recruiting
Phases
Phase 3
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OIC-16008402
Enrollment
Unknown
Registered
2016-05-01
Start date
2016-05-01
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

lymphoplasmacytic lymphoma / Waldenstrom macroglobulinemia

Interventions

Sponsors

Institute of Hematology Blood Disease Hospital, Chinese Academy of Medical Sciences Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years; 2. diagnosed with LPL/WM; 3. Untreated or mild treated without standard regimens,especially untreated with rituximab and/or bortizomib; 4. symptom patients; 5. with life-expectary more than 3 months.

Exclusion criteria

Exclusion criteria: 1. diagnosed with other malignancies outside B-NHL within one year(including active centre neural system lymphoma); 2. Transformed lymphoma; 3. liver or renal funcation lesion unrelated to lymphoma; 4. serious complications such as uncontroled diabetes,gastric ulcer or other serious angiocardiopathy determined by the physician; 5. HIV positive or active HBV infection or other uncontroled systematic infection; 6. clincial central nervous dysfunction; 7. serious surgery within 30 days; 8. pregnancy or baby nursing period or uncontracept child-bearing period woman; 9. allergy to the trail drugs.

Design outcomes

Primary

MeasureTime frame
overall response rate;

Secondary

MeasureTime frame
complete remission rate;

Countries

China

Contacts

Public ContactShuhua Yi

Institute of Hematology Blood Disease Hospital, Chinese Academy of Medical Sciences Peking Union Medical College

shuhuayilove@163.com+86 15900265415

Outcome results

None listed

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