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Tolerability and efficiency of induction and consolidation therapy with ATO, AA, bortezomib and dexamethasone (ABCD) in newly diagnosed myeloma patients-comparison with bortezomib/dexamethasone regimen

Tolerability and efficiency of induction and consolidation therapy with ATO, AA, bortezomib and dexamethasone (ABCD) in newly diagnosed myeloma patients-comparison with bortezomib/dexamethasone regimen

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018811
Enrollment
Unknown
Registered
2018-10-10
Start date
2019-01-01
Completion date
Unknown
Last updated
2018-10-15

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

Conditions

Multiple Myeloma

Interventions

ABCD group:ABCDChemotherapy

Sponsors

Huadong Hospital Affiliated To Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Blood, urine immunofixation electrophoresis, bone marrow examination and cytogenetics, CRAB symptoms, SLiM symptoms, diagnosis of active multiple myeloma under the IMWG standard (symptomatic myeloma); 2) The ECOG score is 0 to 3; 3) Liver function is sound (BUN = 1.5 times the reference value, SGPT = 2 times the reference value); 4) Women of childbearing age are required to undergo a pregnancy test before receiving treatment and must agree to take effective contraceptive measures during treatment; 5) Subjects must sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1) has been diagnosed as hematological tumor; 2) Those who have participated in other clinical trials within 30 days; 3) pregnant and breast-feeding patients; 4) Have received any treatment for this tumor in the past 3 years, but remove superficial bladder cancer, basal cells or squamous cell carcinoma of the skin, cervical intraepithelial neoplasia (CIN) or prostate intraepithelial neoplasia (PIN)); 5) Active viral or bacterial infections that are not controlled by appropriate anti-infective treatment; 6) The serological response of HIV or active hepatitis C virus is known to be positive; 7) suffering from mental illness or other conditions that do not meet the requirements of research treatment and monitoring; 8) bone marrow evacuation; 9) Those who are known to be allergic to any of the ingredients in the protocol; He has received bortezomib or has received a hematopoietic stem cell transplant in the past year.

Design outcomes

Primary

MeasureTime frame
Total effectiveness of induction therapy;OS;PFS;

Countries

China

Contacts

Public ContactXie Yanhui

Huadong Hospital Affiliated To Fudan University

yanhuixie@163.com+86 13321957387

Outcome results

None listed

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