Iron chelation therapy for myelodysplastic syndrome: a systematic review and meta-analysis
Iron chelation therapy for myelodysplastic syndrome: a systematic review and meta-analysis
Liu et al., 2020 | Clin Exp Med | Meta Analysis
Citation
Liu Hailing, Yang Nan, ... Zhang Wanggang. Iron chelation therapy for myelodysplastic syndrome: a systematic review and meta-analysis. Clin Exp Med. 2020-Feb;20(1):1-9. doi:10.1007/s10238-019-00592-5
Abstract
Iron overload remains a concern in myelodysplastic syndrome (MDS) patients especially those requiring recurrent blood transfusions. Whether iron chelating therapy (ICT) is beneficial to the long-term survival of myelodysplastic syndrome is still a controversial issue. Therefore, we conducted a systematic review and meta-analysis to clarify the relationship between ICT and long-term survival in patients with MDS. A total of 14 studies involving 7242 participants were identified; the outcomes revealed that for patients with MDS, ICT resulted in a lower risk of mortality compared to those with no ICT (HR 0.57; 95% CI 0.44-0.70; P < 0.001); what is more, ICT led to a lower risk of leukemia transformation (HR 0.70; 95% CI 0.52-0.93; P = 0.016). Results of subgroup analyses based on adequate ICT or any ICT, low/int-1 IPSS or unclassified IPSS and study types indicated that the ICT had a beneficial role in all these groups of patients.
Key Findings
Results of subgroup analyses based on adequate ICT or any ICT, low/int-1 IPSS or unclassified IPSS and study types indicated that the ICT had a beneficial role in all these groups of patients.
Outcomes Measured
- Requires manual extraction
Population
| Field | Value |
|---|---|
| Population | mds |
| Sample Size | 7242 |
| Age Range | See abstract |
| Condition | See abstract |
MeSH Terms
- Chelation Therapy
- Humans
- Iron
- Iron Overload
- Myelodysplastic Syndromes
- Survival Analysis
- Treatment Outcome
Evidence Classification
- Level: Meta Analysis
- Publication Types: Journal Article, Meta-Analysis, Systematic Review
- Vertical: iron
Provenance
- PMID: 31712933
- DOI: 10.1007/s10238-019-00592-5
- PMCID: Not in PMC
- Verified: 2026-04-09 via PubMed E-utilities API
Source extracted via PubMed E-utilities API on 2026-04-09