Table 1.

Patient and disease characteristics


Data

No.
Number of patients studied   56  
Patient age, y, range (median)   10-66 (43)  
Patient sex, M/F   28/28  
Disease duration, mo, range (median)   3-312 (33)  
Primary diagnosis  
   IMF   33  
   ET with myelofibrosis   10  
   P vera with myelofibrosis   5  
   Myelofibrosis with increased blasts*  5  
   Other  3  
Degree of marrow fibrosis  
   1 (mild)   21  
   2 (moderate)   17  
   3 (severe)   18  
Dupriez classification at transplantation§  
   Good   25  
   Intermediate   17  
   Poor   13  
Platelet count at transplantation  
   100 × 109/L or higher   40  
   Less than 100 × 109/L   15  
Prior splenectomy  
   Yes/no
 
20/36
 

Data

No.
Number of patients studied   56  
Patient age, y, range (median)   10-66 (43)  
Patient sex, M/F   28/28  
Disease duration, mo, range (median)   3-312 (33)  
Primary diagnosis  
   IMF   33  
   ET with myelofibrosis   10  
   P vera with myelofibrosis   5  
   Myelofibrosis with increased blasts*  5  
   Other  3  
Degree of marrow fibrosis  
   1 (mild)   21  
   2 (moderate)   17  
   3 (severe)   18  
Dupriez classification at transplantation§  
   Good   25  
   Intermediate   17  
   Poor   13  
Platelet count at transplantation  
   100 × 109/L or higher   40  
   Less than 100 × 109/L   15  
Prior splenectomy  
   Yes/no
 
20/36
 

IMF indicates idiopathic myelofibrosis; ET, essential thrombocythemia; and P vera, polycythemia vera.

*

All 5 patients had IMF

One patient had IMF that evolved to CML. There were 2 patients who had evidence of NHL in lymph nodes, suggesting the synchronous occurrence of 2 malignancies

According to Guardiola et al.13 

§

Data were incomplete for one patient

Counts were not available for one patient

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