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. 2021 Jun 23;13(13):3142. doi: 10.3390/cancers13133142
AH Anaplastic histology
AHWT Anaplastic histology Wilms tumor
AIEOP Associazione Italiana Ematologia Oncologia Pediatrica
COG-RTC Children’s Oncology Group Renal Tumor Committee
CT Computed tomography
Cy Cyclophosphamide
DA Diffuse anaplasia
Dox Doxorubicin
EFS Event-free survival
ERN PaedCan European Reference Network–Paediatric Cancer
ExPO-r-Net European Expert Paediatric Oncology Reference Network for Diagnostics and Treatment
FA Focal anaplasia
FHWT Favorable histology Wilms tumor
GFAOP French African Pediatric Oncology Group
GPOH Gesellschaft für pädiatrische Onkologie und Hämatologie
HR High risk
IMRT Intensity Modulated RadioTherapy
IR Intermediate risk
JWiTS Japan Wilms Tumor Study
LOH Loss of heterozygosity
LOI Loss of imprinting
LR Low risk
miRNAPGs microRNA processing genes
MIS Minimally invasive surgery
MVA Multivariable analysis
N Number of patients
NA Not applicable
n.s. Not significant
NSS Nephron-sparing surgery
NWTSG National Wilms Tumor Study Group
OS Overall survival
PODC Pediatric Oncology in Developing Countries
Ref Reference
RFS Recurrence-free survival
SIOP-RTSG International Society of Pediatric Oncology Renal Tumor Study Group
UKCCLG United Kingdom Children’s Cancer and Leukaemia Group
UVA Univariable analysis
VA Vincristin, Actinomycin-D
VAD Vincristin, Actinomycin-D and Doxorubicin
VLRWT Very low risk Wilms tumor
WAGR Wilms tumor, aniridia, genitourinary anomalies, and range of developmental delays
WT Wilms tumor