TY - JOUR
T1 - SEIFEM 2017
T2 - from real life to an agreement on the use of granulocyte transfusions and colony-stimulating factors for prophylaxis and treatment of infectious complications in patients with hematologic malignant disorders
AU - SEIFEM group (Sorveglianza Epidemiologica Infezioni Fungine in Ematologia)
AU - Busca, Alessandro
AU - Cesaro, Simone
AU - Teofili, Luciana
AU - Delia, Mario
AU - Cattaneo, Chiara
AU - Criscuolo, Marianna
AU - Marchesi, Francesco
AU - Fracchiolla, Nicola Stefano
AU - Valentini, Caterina Giovanna
AU - Farina, Francesca
AU - Di Blasi, Roberta
AU - Prezioso, Lucia
AU - Spolzino, Angelica
AU - Candoni, Anna
AU - Del Principe, Maria Ilaria
AU - Verga, Luisa
AU - Nosari, Annamaria
AU - Aversa, Franco
AU - Pagano, Livio
PY - 2018/2
Y1 - 2018/2
N2 - INTRODUCTION: The rapid spread of severe infections mainly due to resistant pathogens, justifies the search for therapies aiming to restore immune functions severely compromised in patients with hematologic malignancies. Areas covered: The present review summarizes the current knowledge on the role of granulocyte transfusions and colony-stimulating factors as treatment strategy for hematologic patients with serious infectious complications. In addition, a survey among 21 hematologic centers, to evaluate the clinical practice for the use of G-CSF originator and biosimilars was performed. Expert commentary: Granulocyte transfusions with a target dose of at least 1.5-3 × 108 cells/kg, may be considered as an approach to bridge the gap between marrow suppression and recovery of granulocytes. G-CSF shortens the period of neutropenia, the hospitalization, the use of antibiotics and the rate of febrile neutropenia (FN) in adult and pediatric patients with non-Hodgkin lymphoma, and in adults with acute myeloid leukemia where these advantages nevertheless, did not translate into a clinical benefit. G-CSF biosimilar showed equivalence or non-inferiority to filgrastim. There are no data supporting the use of GM-CSF, eltrombopag and erythropoietin for preventing or treating infectious complications in patients with hematologic disorders.
AB - INTRODUCTION: The rapid spread of severe infections mainly due to resistant pathogens, justifies the search for therapies aiming to restore immune functions severely compromised in patients with hematologic malignancies. Areas covered: The present review summarizes the current knowledge on the role of granulocyte transfusions and colony-stimulating factors as treatment strategy for hematologic patients with serious infectious complications. In addition, a survey among 21 hematologic centers, to evaluate the clinical practice for the use of G-CSF originator and biosimilars was performed. Expert commentary: Granulocyte transfusions with a target dose of at least 1.5-3 × 108 cells/kg, may be considered as an approach to bridge the gap between marrow suppression and recovery of granulocytes. G-CSF shortens the period of neutropenia, the hospitalization, the use of antibiotics and the rate of febrile neutropenia (FN) in adult and pediatric patients with non-Hodgkin lymphoma, and in adults with acute myeloid leukemia where these advantages nevertheless, did not translate into a clinical benefit. G-CSF biosimilar showed equivalence or non-inferiority to filgrastim. There are no data supporting the use of GM-CSF, eltrombopag and erythropoietin for preventing or treating infectious complications in patients with hematologic disorders.
KW - Adolescent
KW - Adult
KW - Anti-Bacterial Agents/therapeutic use
KW - Child
KW - Child, Preschool
KW - Colony-Stimulating Factors/therapeutic use
KW - Female
KW - Granulocytes
KW - Hematologic Neoplasms/complications
KW - Humans
KW - Infection/etiology
KW - Leukemia, Myeloid, Acute/complications
KW - Leukocyte Transfusion
KW - Lymphoma, Non-Hodgkin/complications
KW - Male
KW - Neutropenia/complications
U2 - 10.1080/17474086.2018.1420472
DO - 10.1080/17474086.2018.1420472
M3 - Article
C2 - 29285951
VL - 11
SP - 155
EP - 168
JO - Expert Review of Hematology
JF - Expert Review of Hematology
SN - 1747-4086
IS - 2
ER -