Abstract
Background: Matched donor (MD) allogeneic hematopoietic stem cell transplantation (allo-HSCT) is currently the preferred choice of treatment for Philadelphia chromosome-positive acute lymphoblastic leukemia (Phþ ALL) patients who have achieved complete remission. This systematic review and meta-analysis was conducted to investigate the effects of allo-HSCTs from different donor types for Phþ ALL patients who received tyrosine kinase inhibitors (TKIs). Methods: Studies in EMBASE and MEDLINE between inception and December 2020 were identified using search terms related to “Phþ ALL” and “HSCT.” Eligible studies were studies with Phþ ALL patients who received a TKI and allo-HSCT. The primary outcomes of interestdthe overall survival (OS) or relapse-free survival (RFS)dneeded to be reported. The ManteleHaenszel method was used to combine the effect estimates and associated 95% confidence intervals (CIs) of each donor type. Results: Fourteen cohort studies were identified for the meta-analysis. Haploidentical (HID)-HSCT for Phþ ALL patients resulted in a superior RFS to MD-HSCT, with a pooled odds ratio (OR) of 1.57 (95% CI, 1.05e2.32; I2 ¼ 0%). However, HID-HSCT and MD-HSCT had comparable OS. Furthermore, HID-HSCT group had a significantly lower relapse rate than MD-HSCT group. On the other hand, the risks of graft-versus-host disease (GvHD) were higher for HID-HSCT and pooled OR of chronic GvHD rate. The OS and RFS of matched sibling-HSCT, matched unrelated-HSCT, and cord blood-HSCT were comparable with those of HID-HSCT. Conclusion: This systematic review and meta-analysis showed that HID-HSCT is as effective as MD-HSCT in Phþ ALL patients.
| Original language | English |
|---|---|
| Pages (from-to) | 197-208 |
| Number of pages | 12 |
| Journal | Hematology/ Oncology and Stem Cell Therapy |
| Volume | 16 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 2023 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Acute lymphoblastic leukemia
- Allogeneic stem cell transplantation
- BCR-ABL
- Haploidentical donor
- Ph ALL
- Philadelphia chromosome
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