4.6 Article

Non-infectious causes of elevated procalcitonin and C-reactive protein serum levels in pediatric patients with hematologic and oncologic disorders

Journal

SUPPORTIVE CARE IN CANCER
Volume 16, Issue 9, Pages 1035-1040

Publisher

SPRINGER
DOI: 10.1007/s00520-007-0381-1

Keywords

procalcitonin; CRP; T-cell antibodies; interleukin-2; granulocyte transfusion; GvHD

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Background Procalcitonin (PCT) is considered a sensitive and specific diagnostic and prognostic marker of systemic bacterial infection, but its value is questionable in certain clinical conditions, particularly in hemato-oncological patients. Materials and methods We analyzed PCT and C-reactive protein (CRP) levels in 56 patients of a pediatric hematology-oncology unit during 110 consecutive non-infectious febrile episodes related to administration of T-cell antibodies (group A; n=22), alemtuzumab (monoclonal CD52 antibody, CAMPATH-1H/group B; n=8), interleukin-2 (IL-2/group C; n=41), prophylactic donor granulocyte transfusions (group D; n=9), or to acute graft-versus-host disease (aGvHD/group E; n=10) and compared the results with 20 episodes of Gram-negative sepsis (group F). Main results In the majority of the non-infectious episodes PCT and CRP increased to serum levels statistically indistinguishable from Gram-negative sepsis. Median peak levels of PCT (normal < 0.5 ng/ml)/CRP (normal < 8 mg/l) for groups A-F were 4.34/59.0 (A), 10.14/93.5 (B), 1.11/175.0 (C), 1.43/164 (D), 0.96/34.0 (E), and 8.14 ng/ml /126.0 mg/l (F). Highest single levels were observed in groups A and F. Conclusions PCT and CRP are of limited value as diagnostic markers of sepsis during T-cell-directed immunomodulatory treatment, granulocyte support, or acute GvHD.

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