TY - JOUR
T1 - Progression of localised Wilms' tumour during preoperative chemotherapy is an independent prognostic factor
T2 - A report from the SIOP 93-01 nephroblastoma trial and study
AU - Øra, Ingrid
AU - van Tinteren, Harm
AU - Bergeron, Christophe
AU - de Kraker, Jan
N1 - Funding Information:
This study was supported by grants from the Stichting Kindergeneeskundig Kankeronderzoek and the Swedish Children Cancer Foundation.
PY - 2007/1
Y1 - 2007/1
N2 - The SIOP nephroblastoma clinical trials have previously demonstrated that preoperative chemotherapy is advantageous for patients with nephroblastoma (Wilms' tumour). However, some primary tumours increase in size during preoperative chemotherapy, and to investigate the clinical relevance of this progression we studied the patient cohort with increasing tumours included in the SIOP 93-01 study (June 1993 to June 2000). Patients were considered eligible if they had a confirmed localised Wilms' tumour that had been measured in at least two dimensions at diagnosis and before surgery. Tumour response to preoperative chemotherapy was defined according to criteria set by the World Health Organisation (WHO). Patient characteristics in the different response groups were compared and related to event-free survival and overall survival. Patient records were studied regarding compliance with protocol. Tumour progression during preoperative chemotherapy was observed in 57 of 1090 patients (5%) with localised Wilms' tumours. In those cases, the tumours were significantly smaller at diagnosis and were more often stage III (p = 0.05) and associated with high risk histopathology (p = 0.03). After adjustment for stage and risk group, progression was proved to be correlated with poorer event-free and overall survival (hazard ratio 1.9, p = 0.026 and 3.2, p = 0.002 respectively). In summary, progression of localised Wilms' tumours is rarely seen in patients during preoperative chemotherapy. However, independent of stage distribution and histopathological risk group, those whose tumours do increase in size have poorer event-free and overall survival.
AB - The SIOP nephroblastoma clinical trials have previously demonstrated that preoperative chemotherapy is advantageous for patients with nephroblastoma (Wilms' tumour). However, some primary tumours increase in size during preoperative chemotherapy, and to investigate the clinical relevance of this progression we studied the patient cohort with increasing tumours included in the SIOP 93-01 study (June 1993 to June 2000). Patients were considered eligible if they had a confirmed localised Wilms' tumour that had been measured in at least two dimensions at diagnosis and before surgery. Tumour response to preoperative chemotherapy was defined according to criteria set by the World Health Organisation (WHO). Patient characteristics in the different response groups were compared and related to event-free survival and overall survival. Patient records were studied regarding compliance with protocol. Tumour progression during preoperative chemotherapy was observed in 57 of 1090 patients (5%) with localised Wilms' tumours. In those cases, the tumours were significantly smaller at diagnosis and were more often stage III (p = 0.05) and associated with high risk histopathology (p = 0.03). After adjustment for stage and risk group, progression was proved to be correlated with poorer event-free and overall survival (hazard ratio 1.9, p = 0.026 and 3.2, p = 0.002 respectively). In summary, progression of localised Wilms' tumours is rarely seen in patients during preoperative chemotherapy. However, independent of stage distribution and histopathological risk group, those whose tumours do increase in size have poorer event-free and overall survival.
KW - Clinical tumour response
KW - Event-free survival
KW - Histopathological risk group
KW - Nephroblastoma
KW - Overall survival
KW - Preoperative chemotherapy
KW - Prognostic factor
KW - Tumour response evaluation
KW - Wilms' tumour
UR - http://www.scopus.com/inward/record.url?scp=33845976672&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2006.08.033
DO - 10.1016/j.ejca.2006.08.033
M3 - Article
C2 - 17084075
AN - SCOPUS:33845976672
SN - 0959-8049
VL - 43
SP - 131
EP - 136
JO - European Journal of Cancer
JF - European Journal of Cancer
IS - 1
ER -