Title : Plasma protein C is a useful clinical marker for hepatic veno-occlusive disease (VOD) in stem cell transplantation - Iguchi_2010_Pediatr.Blood.Cancer_54_437 |
Author(s) : Iguchi A , Kobayashi R , Kaneda M , Kobayashi K |
Ref : Pediatr Blood Cancer , 54 :437 , 2010 |
Abstract :
BACKGROUND: Hepatic veno-occlusive disease (VOD) is one of the most serious complications in stem cell transplantation (SCT). Although plasma protein C activity decreases in VOD after SCT, the timeframe of plasma protein C activity decreases during SCT is not known. PROCEDURE: We examined levels of plasma protein C serially during the course of SCT to determine the critical level and risk factors for VOD. RESULTS: Of 151 children who received SCT, 12 of them (7.9%) developed VOD. The mean minimum protein C activity in patients with VOD was significantly lower compared to that in patients without VOD (P < 0.0001). Receiver operating characteristic curve analysis revealed that the critical plasma protein C activity (cut-off point) for VOD was identified to be 34.5% with high sensitivity (100%) and specificity (83.3%), and the reduction of plasma protein C below the cut-off level (day +6.50 +/- 2.43) was observed mostly prior to the onset of VOD (day +7.33 +/- 2.64). The patients receiving melphalan in conditioning were found to be at high risk for VOD (P = 0.003). Among the melphalan containing regimens, melphalan + carboplatin + etoposide was a significant risk factor for depression of plasma protein C (P = 0.037). CONCLUSION: Plasma protein C level was a useful parameter of VOD after SCT, and activity below 34.5% was critical for VOD. The use of melphalan in conditioning causes a high risk for VOD. |
PubMedSearch : Iguchi_2010_Pediatr.Blood.Cancer_54_437 |
PubMedID: 19911420 |
Iguchi A, Kobayashi R, Kaneda M, Kobayashi K (2010)
Plasma protein C is a useful clinical marker for hepatic veno-occlusive disease (VOD) in stem cell transplantation
Pediatr Blood Cancer
54 :437
Iguchi A, Kobayashi R, Kaneda M, Kobayashi K (2010)
Pediatr Blood Cancer
54 :437