Table 3.

Comparison between non–HCT-OP and HCT-OP

Non–HCT-OPHCT-OP
Patient population  
Rarely reported in children Any allogeneic HCT recipient 
Can be cryptogenic or associated with other processes (infection, drug toxicity, or radiation) Isolated occurrence without other GVHD in other organs is rare
Associated with GVHD of other organs, especially mouth and skin 
Diagnosis  
Lung biopsy is pursued to confirm diagnosis or rule out secondary causes Lung biopsy is reserved for selective cases given the high risk of postprocedural complications 
Lower lung zone preference No zonal preference 
Recurrence can present with migratory opacities or different radiographic features as to index event Recurrence tends to occur at the same location with similar radiographic features as to index event 
Treatment  
Spontaneous resolution can be observed Spontaneous resolution is rare 
Extended period of corticosteroid for 6-12 mo may be necessary Extended corticosteroid course >6-12 mo is often required 
Prognosis  
Relapse rate of 13%-58%7  Relapse rate of 30%-50% 
Mortality is <10%; death often unrelated to OP Higher death rate from respiratory failure12  
Excellent prognosis, with 5-y survival >90%1  Prognosis is less favorable20  
Corticosteroid-sparing agents   
Mycophenolate mofetil, azithromycin, cyclosporine, rituximab Mycophenolate mofetil, ruxolitinib, cyclosporine 
Non–HCT-OPHCT-OP
Patient population  
Rarely reported in children Any allogeneic HCT recipient 
Can be cryptogenic or associated with other processes (infection, drug toxicity, or radiation) Isolated occurrence without other GVHD in other organs is rare
Associated with GVHD of other organs, especially mouth and skin 
Diagnosis  
Lung biopsy is pursued to confirm diagnosis or rule out secondary causes Lung biopsy is reserved for selective cases given the high risk of postprocedural complications 
Lower lung zone preference No zonal preference 
Recurrence can present with migratory opacities or different radiographic features as to index event Recurrence tends to occur at the same location with similar radiographic features as to index event 
Treatment  
Spontaneous resolution can be observed Spontaneous resolution is rare 
Extended period of corticosteroid for 6-12 mo may be necessary Extended corticosteroid course >6-12 mo is often required 
Prognosis  
Relapse rate of 13%-58%7  Relapse rate of 30%-50% 
Mortality is <10%; death often unrelated to OP Higher death rate from respiratory failure12  
Excellent prognosis, with 5-y survival >90%1  Prognosis is less favorable20  
Corticosteroid-sparing agents   
Mycophenolate mofetil, azithromycin, cyclosporine, rituximab Mycophenolate mofetil, ruxolitinib, cyclosporine 

Refer to Table 4 for detail.

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