Skip to content

The efficacy and safety of magnesium isoglycyrrhizinate in preventing novel antitumor drug-related liver injury in patients with malignant hematological diseases: A multicenter, retrospective study

The efficacy and safety of magnesium isoglycyrrhizinate in preventing novel antitumor drug-related liver injury in patients with malignant hematological diseases: A multicenter, retrospective study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500100629
Enrollment
Unknown
Registered
2025-04-11
Start date
2024-05-15
Completion date
Unknown
Last updated
2025-04-14

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

Conditions

Hematologic Malignancy

Interventions

Control group: conventional anti-tumor therapy without any preventive liver protection treatment:None
Observation group: conventional anti-tumor therapy + magnesium isoglycyrrhizinate preventive liver protection therapy:None

Sponsors

China Academy of Medical Sciences Blood Disease Hospital (China Academy of Medical Sciences Hematology Institute)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients with hematological malignancies (including but not limited to lymphoma, myeloma, leukemia); 2. Age >= 18 years; 3. Patients with at least one new anti-tumor drug in the anti-tumor treatment regimen *; 4. The use of magnesium isoglycyrrhizinate to prevent liver injury treatment time is the first course of anti-tumor therapy on the day or before (magnesium isoglycyrrhizinate dose >= 150 mg/day, and medication duration >= 5 days); 5.TBiL <= 1.0 × ULN; ALT, AST <= 1.0 × ULN; ALP <= 1.0 × ULN before magnesium isoglycyrrhizinate prophylaxis;

Exclusion criteria

Exclusion criteria: 1.Patients using other types of hepatoprotective drugs except magnesium isoglycyrrhizinate (such as polyene phosphatidylcholine, reduced glutathione and tiopronin, etc.); 2. Patients with combined liver local radiotherapy; 3. Patients combined with cellular immunotherapy *; 4. Patients with hepatitis B or hepatitis C virus in a replicative state and requiring antiviral therapy; 5. Patients who lack key clinical data information such as liver function indicators and cannot make clinical judgment on the diagnosis of liver injury related to anti-tumor drugs; * Cellular immunotherapy includes cytokine-induced killer cell therapy, dendritic cell therapy, DC + CIK cell therapy, natural killer cell therapy, and DC ~ T cell therapy.

Design outcomes

Primary

MeasureTime frame
Incidence and severity of liver injury within 21 days, 30 days and 60 days of magnesium isoglycyrrhizinate prophylaxis;

Secondary

MeasureTime frame
Safety;

Countries

China

Contacts

Public ContactErlie Jiang

China Academy of Medical Sciences Blood Disease Hospital (China Academy of Medical Sciences Hematology Institute)

jiangerlie@ihcams.ac.cn+86 132 3303 4461

Outcome results

None listed

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