Clinical factors | |
 Decreased performance status | |
 Increased number of comorbidities | |
 Decreased organ function | |
 Polypharmacy | |
 Frequent dose reductions, delays, or omission | |
 Higher risk of adverse events (infections, neurotoxicity, secondary malignancies) | |
Biological factors | |
 Increased incidence of adverse-risk karyotype (e.g., low hypodiploidy/near-triploidy, t(9;22), t(4;11), complex cytogenetics) | |
 Lower incidence of favorable-risk karyotype (hyperdiploidy, t(12;21), ETV6-RUNX1) | |
 Higher incidence of adverse risk molecular signatures (Philadelphia chromosome-like, TP53 mutation) | |
Social factors | |
 Inadequate caregiver and/or social support | |
 Transportation/travel difficulties to tertiary centers | |
Other factors | |
 Perceived lack of benefit of receiving anti-leukemia therapy rather than supportive/hospice care |