Simone Cesaro

Dr. Simone Cesaro

Azienda Ospedaliera Universitaria Integrata Verona, Verona, Veneto, Italy
+1
orcid

Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
7 May 2020 in New England Journal of Medicine
Verified
Journal Article
Closed access
FLFranco Locatelli
Franco Locatelli
MJMichael B. Jordan
Michael B. Jordan
CACarl Allen
Carl Allen
Simone CesaroSimone Cesaro
Simone Cesaro
CRCarmelo Rizzari
Carmelo Rizzari
CMCristina de Min
Cristina de Min
Primary hemophagocytic lymphohistiocytosis is a rare syndrome characterized by immune dysregulation and hyperinflammation. It typically manifests in infancy and is associated with high mortality.

22 February 2016 in Bone Marrow Transplantation
Verified
Journal Article
Open access
PDF file
JPJakob R Passweg
Jakob R Passweg
HBH Baldomero
H Baldomero
PBP Bader
P Bader
CBC Bonini
C Bonini
Simone CesaroSimone Cesaro
Simone Cesaro
MMM Mohty
M Mohty
A record number of 40 829 hematopoietic stem cell transplantation (HSCT) in 36 469 patients (15 765 allogeneic (43%), 20 704 autologous (57%)) were reported by 656 centers in 47 countries to the 2014 survey. Trends include: continued growth in transplant activity, more so in Eastern European countries than in the west; a continued increase in the use of haploidentical family donors (by 25%) and slower growth for unrelated donor HSCT. The use of cord blood as a stem cell source has decreased again in 2014. Main indications for HSCT were leukemias: 11 853 (33%; 96% allogeneic); lymphoid neoplasias; 20 802 (57%; 11% allogeneic); solid tumors; 1458 (4%; 3% allogeneic) and non-malignant disorders; 2203 (6%; 88% allogeneic). Changes in transplant activity include more allogeneic HSCT for AML in CR1, myeloproliferative neoplasm (MPN) and aplastic anemia and decreasing use in CLL; and more autologous HSCT for plasma cell disorders and in particular for amyloidosis. In addition, data on numbers of teams doing alternative donor transplants, allogeneic after autologous HSCT, autologous cord blood transplants are presented.

1 July 2014 in The Lancet Oncology
Verified
Journal Article
Closed access
Andreas Hermann GrollAndreas Hermann Groll
Andreas Hermann Groll
ECElio Castagnola
Elio Castagnola
Simone CesaroSimone Cesaro
Simone Cesaro
JDJean-Hugues Dalle
Jean-Hugues Dalle
DEDan Engelhard
Dan Engelhard
TLThomas Lehrnbecher
Thomas Lehrnbecher

27 August 2019 in Bone Marrow Transplantation
Verified
Journal Article
Open access
PDF file
FEFor The Infectious Diseases Working Party Ebmt
For The Infectious Diseases Working Party Ebmt
JSJan Styczyński
Jan Styczyński
GTGloria Tridello
Gloria Tridello
LKLinda Koster
Linda Koster
SISimona Iacobelli
Simona Iacobelli
AGAlois Gratwohl
Alois Gratwohl
Information on incidence, and factors associated with mortality is a prerequisite to improve outcome after hematopoietic stem cell transplantation (HSCT). Therefore, 55′668 deaths in 114′491 patients with HSCT (83.7% allogeneic) for leukemia were investigated in a landmark analysis for causes of death at day 30 (very early), day 100 (early), at 1 year (intermediate) and at 5 years (late). Mortality from all causes decreased from cohort 1 (1980–2001) to cohort 2 (2002–2015) in all post-transplant phases after autologous HSCT. After allogeneic HSCT, mortality from infections, GVHD, and toxicity decreased up to 1 year, increased at 5 years; deaths from relapse increased in all post-transplant phases. Infections of unknown origin were the main cause of infectious deaths. Lethal bacterial and fungal infections decreased from cohort 1 to cohort 2, not unknown or mixed infections. Infectious deaths were associated with patient-, disease-, donor type, stem cell source, center, and country- related factors. Their impact varied over the post-transplant phases. Transplant centres have successfully managed to reduce death after HSCT in the early and intermediate post-transplant phases, and have identified risk factors. Late post-transplant care could be improved by focus on groups at risk and better identification of infections of “unknown origin”.

1 April 2012 in The Lancet
Verified
Journal Article
Closed access
SCSelim Corbacioglu
Selim Corbacioglu
Simone CesaroSimone Cesaro
Simone Cesaro
MFMaura Faraci
Maura Faraci
DVDominique Valteau-Couanet
Dominique Valteau-Couanet
BGBernd Gruhn
Bernd Gruhn
GDGiorgio Dini
Giorgio Dini

31 July 2017 in Bone Marrow Transplantation
Verified
Journal Article
Open access
PDF file
SCS Corbacioglu
S Corbacioglu
ECE Carreras
E Carreras
MAM Ansari
M Ansari
ABA Balduzzi
A Balduzzi
Simone CesaroSimone Cesaro
Simone Cesaro
PBP Bader
P Bader
The advances in hematopoietic cell transplantation (HCT) over the last decade have led to a transplant-related mortality below 15%. Hepatic sinusoidal obstruction syndrome/veno-occlusive disease (SOS/VOD) is a life-threatening complication of HCT that belongs to a group of diseases increasingly identified as transplant-related, systemic endothelial diseases. In most cases, SOS/VOD resolves within weeks; however, severe SOS/VOD results in multi-organ dysfunction/failure with a mortality rate >80%. A timely diagnosis of SOS/VOD is of critical importance, given the availability of therapeutic options with favorable tolerability. Current diagnostic criteria are used for adults and children. However, over the last decade it has become clear that SOS/VOD is significantly different between the age groups in terms of incidence, genetic predisposition, clinical presentation, prevention, treatment and outcome. Improved understanding of SOS/VOD and the availability of effective treatment questions the use of the Baltimore and Seattle criteria for diagnosing SOS/VOD in children. The aim of this position paper is to propose new diagnostic and severity criteria for SOS/VOD in children on behalf of the European Society for Blood and Marrow Transplantation.