TY - JOUR
T1 - Prediction of infectious complications by the combination of plasma procalcitonin level and localized infection before allogeneic hematopoietic cell transplantation
AU - Sato, M.
AU - Nakasone, H.
AU - Terasako-Saito, K.
AU - Sakamoto, K.
AU - Yamazaki, R.
AU - Tanaka, Y.
AU - Akahoshi, Y.
AU - Nakano, H.
AU - Ugai, T.
AU - Wada, H.
AU - Yamasaki, R.
AU - Ishihara, Y.
AU - Kawamura, K.
AU - Ashizawa, M.
AU - Kimura, S. I.
AU - Kikuchi, M.
AU - Tanihara, A.
AU - Kanda, J.
AU - Kako, S.
AU - Nishida, J.
AU - Kanda, Y.
PY - 2014/4
Y1 - 2014/4
N2 - We previously reported that the baseline C-reactive protein level did not predict infectious events after hematopoietic cell transplantation (HCT). Procalcitonin (PCT) has recently emerged as a powerful biomarker for the early diagnosis of bacterial infection. We evaluated the ability of the baseline PCT level to predict early infectious events after HCT in 79 recipients who received HCT between 2008 and 2012. The high-PCT group (≥0.07 ng/mL, n=27) frequently experienced documented infection (DI) (21.2% vs 44.4% at day 30, P=0.038) and bloodstream infection (BSI) (15.4% vs 37.0% at day 30, P=0.035). In a multivariate analysis, however, the baseline PCT level was not significantly associated with DI (HR 2.01, P=0.089) or BSI (HR 2.28, P=0.084). Localized infection, such as anal canal problems, before the start of conditioning was seen in 26 patients. When we stratified the patients according to the presence of elevated PCT and localized infection, the group with elevated PCT and localized infection (n=17) was significantly associated with increased DI (HR 3.40, P=0.0074) and BSI (HR 3.59 P=0.0078) after HCT. A larger prospective observation is warranted to confirm the impact of the baseline PCT level and clinical features on the outcome of HCT.
AB - We previously reported that the baseline C-reactive protein level did not predict infectious events after hematopoietic cell transplantation (HCT). Procalcitonin (PCT) has recently emerged as a powerful biomarker for the early diagnosis of bacterial infection. We evaluated the ability of the baseline PCT level to predict early infectious events after HCT in 79 recipients who received HCT between 2008 and 2012. The high-PCT group (≥0.07 ng/mL, n=27) frequently experienced documented infection (DI) (21.2% vs 44.4% at day 30, P=0.038) and bloodstream infection (BSI) (15.4% vs 37.0% at day 30, P=0.035). In a multivariate analysis, however, the baseline PCT level was not significantly associated with DI (HR 2.01, P=0.089) or BSI (HR 2.28, P=0.084). Localized infection, such as anal canal problems, before the start of conditioning was seen in 26 patients. When we stratified the patients according to the presence of elevated PCT and localized infection, the group with elevated PCT and localized infection (n=17) was significantly associated with increased DI (HR 3.40, P=0.0074) and BSI (HR 3.59 P=0.0078) after HCT. A larger prospective observation is warranted to confirm the impact of the baseline PCT level and clinical features on the outcome of HCT.
KW - Allogeneic hematopoietic cell transplantation
KW - Infectious events
KW - Procalcitonin
KW - Transplant-related complications
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U2 - 10.1038/bmt.2013.217
DO - 10.1038/bmt.2013.217
M3 - Article
C2 - 24419514
AN - SCOPUS:84897530021
SN - 0268-3369
VL - 49
SP - 553
EP - 560
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 4
ER -