Table 1.

Considerations that influence the decision to initiate maintenance therapy after allogeneic HCT

FactorConsiderations
Underlying disease Higher rates of relapse for high-risk disease characteristics (elevated blast count, specific cytogenetic or molecular abnormalities) compared with the absence of high-risk disease factors 
Disease status at transplant Higher rates of relapse in acute leukemia when measurable disease detectable at transplant compared with undetectable disease 
Intensity of the conditioning regimen Higher rates of relapse with reduced intensity conditioning therapy compared with myeloablative conditioning 
Post-HCT complications Slow hematopoietic recovery or ongoing toxicities (GVHD, infection, organ dysfunction) limit ability to initiate maintenance therapies 
Characteristics of therapeutic agent Therapeutic agent must address underlying disease biology (targeted agents for identified mutations or hypomethylating agent-based approached for myeloid neoplasms) and have favorable toxicity profile in post-HCT setting 
FactorConsiderations
Underlying disease Higher rates of relapse for high-risk disease characteristics (elevated blast count, specific cytogenetic or molecular abnormalities) compared with the absence of high-risk disease factors 
Disease status at transplant Higher rates of relapse in acute leukemia when measurable disease detectable at transplant compared with undetectable disease 
Intensity of the conditioning regimen Higher rates of relapse with reduced intensity conditioning therapy compared with myeloablative conditioning 
Post-HCT complications Slow hematopoietic recovery or ongoing toxicities (GVHD, infection, organ dysfunction) limit ability to initiate maintenance therapies 
Characteristics of therapeutic agent Therapeutic agent must address underlying disease biology (targeted agents for identified mutations or hypomethylating agent-based approached for myeloid neoplasms) and have favorable toxicity profile in post-HCT setting 

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