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Meta-Analysis
. 2017 Feb 3;12(2):e0171608.
doi: 10.1371/journal.pone.0171608. eCollection 2017.

Prognostic significance of SETBP1 mutations in myelodysplastic syndromes, chronic myelomonocytic leukemia, and chronic neutrophilic leukemia: A meta-analysis

Affiliations
Meta-Analysis

Prognostic significance of SETBP1 mutations in myelodysplastic syndromes, chronic myelomonocytic leukemia, and chronic neutrophilic leukemia: A meta-analysis

Li-Hong Shou et al. PLoS One. .

Abstract

Objectives: This meta-analysis investigates the prognostic effect of SET binding protein 1 (SETBP1) mutations in patients with myelodysplastic syndromes (MDS), chronic myelomonocytic leukemia (CMML), or chronic neutrophilic leukemia (CNL).

Methods: Eligible studies from Pubmed, Embase, and Web of Science were searched from database inception through April 2016. Hazard ratios (HRs) and 95% confidence interval (CI) of overall survival (OS) were pooled to calculate the prognostic significance of SETBP1 mutation in patients.

Results: A total of 12 studies with 2321 patients were included in this meta-analysis; 4 studies for MDS, 5 studies for CMML, and 3 studies for CNL. Pooled results suggested that MDS and CMML patients with SETBP1 mutations had a significantly poorer prognosis when compared with patients with wild-type SETBP1 (MDS: HR = 1.808, 95% CI (1.218-2.685), P = 0.001; CMML: HR = 2.223, 95% CI (1.493-3.308), P<0.001). SETBP1 mutations in CNL patients however, showed no significant effect on the overall survival (HR = 1.773, 95% CI (0.877-3.582), P = 0.111). The Begg's and Egger's tests did not show significant publication bias in any groups.

Conclusions: Current evidence shows that SETBP1 mutation is associated with a poor prognosis in patients with MDS and CMML, but not in patients with CNL.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Flow chart of study selection.
Fig 2
Fig 2. Forest plot of the HR and 95% CI for OS in MDS patients.
Fig 3
Fig 3. Sensitivity analysis for all included MDS studies.
Fig 4
Fig 4. Begg’s funnel plot of the prognostic significance of SETBP1 mutation in MDS patients.
Fig 5
Fig 5. Forest plot of the HR and 95% CI for OS in CMML patients.
Fig 6
Fig 6. Sensitivity analysis for all included CMML studies.
Fig 7
Fig 7. Begg’s funnel plot of the prognostic significance of SETBP1 mutation in CMML patients.
Fig 8
Fig 8. Forest plot of the HR and 95% CI for OS in CNL patients.
Fig 9
Fig 9. Sensitivity analysis for all included CNL studies.
Fig 10
Fig 10. Begg’s funnel plot of the prognostic significance of SETBP1 mutation in CNL patients.

References

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