Table 2.
Indications of HSCT for CML in the Current Era.
Indication | Summary |
---|---|
Cost-effectiveness in low-income countries | Financial barriers hinder access to TKIs in developing countries, making HSCT a more feasible and cost-effective option. |
Children and young adults | HSCT demonstrates favorable outcomes and may be preferred over lifelong TKI therapy for pediatric and young adult patients. |
Aiming for TFR in CML | Achieving treatment-free remission is a goal; however, HSCT remains the only curative therapy for long-term remission. |
Intolerance and resistance of TKIs | HSCT is recommended for patients resistant or intolerant to TKIs, providing better long-term survival opportunities. |
Blast crisis | HSCT is vital for patients in blast crisis, achieving long-term remission and improved survival rates. |
Advanced accelerated-phase CML | HSCT offers better outcomes than TKIs, particularly in late accelerated-phase cases. |
T315I mutation in CML | Ponatinib is effective for T315I-positive chronic-phase CML, but HSCT should be considered for Ponatinib resistance and advanced stages of CML. |
Concurrent myelodysplastic syndromes | HSCT can lead to complete remission of both myeloid and lymphoid malignancies, providing a potential, curative option. |
Caption: Summary of indications for HSCT in CML based on different clinical scenarios and disease stages. HSCT offers curative potential, better outcomes, and cost-effectiveness in specific patient populations. Abbreviations: TKIs, tyrosine kinase inhibitors; HSCT, hematopoietic stem cell transplantation; TFR, treatment-free remission; CCyR, complete cytogenetic response; OS, overall survival; LFS, leukemia-free survival; EFS, event-free survival; CMR, complete molecular remission; MDS, myelodysplastic syndrome.