Outcomes of non-anaplastic stage III and 'inoperable' Wilms tumour treated in the UKW3 trial.


Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
02 2019
Historique:
received: 05 02 2018
revised: 21 10 2018
accepted: 23 10 2018
entrez: 19 2 2019
pubmed: 19 2 2019
medline: 20 12 2019
Statut: ppublish

Résumé

To describe the outcome of patients with stage III Wilms tumours (WT) treated in the UKW3 trial. Patients with a pathologically confirmed stage III non-anaplastic WT at nephrectomy (Group A) or with an 'inoperable' tumour at diagnosis managed by biopsy and pre-operative chemotherapy (Actinomycin D-Vincristine-Doxorubicin) but stage I or II at subsequent nephrectomy (Group B) were included. The 4-year overall (OS)/event free survival (EFS) for Group A (n = 117) patients was 90%(95%CI:83-94)/81%(CI:73-87) and for Group B (n = 32) 94%(CI:77-98)/88%(CI:70-95). The 4-year OS/EFS of patients with pathological stage III WT according to whether they received flank/abdominal radiotherapy (95 patients) or not (37 patients, 22 from UKW3 pooled with 17 patients from UKW2) were 91%(CI:83-95)/82%(CI:73-89), and 84%(CI:67-92)/78%(CI:61-89), respectively. The 4-year OS/EFS for patients having one reason to be stage III versus two or three was 92%(CI:84-96)/83%(CI:73-90) and 85%(CI:70-93)/78%(CI:61-88), respectively. Our findings question the inclusion of biopsy or pre-operative chemotherapy as sole criterion for assigning a tumour stage III. Selected patients with pathological stage III WT can survive without radiotherapy. Whilst cautious interpretation is needed due to the post hoc nature of these analyses, further biological studies may better characterise those who could benefit from reduced therapy.

Sections du résumé

BACKGROUND AND PURPOSE
To describe the outcome of patients with stage III Wilms tumours (WT) treated in the UKW3 trial.
MATERIAL AND METHODS
Patients with a pathologically confirmed stage III non-anaplastic WT at nephrectomy (Group A) or with an 'inoperable' tumour at diagnosis managed by biopsy and pre-operative chemotherapy (Actinomycin D-Vincristine-Doxorubicin) but stage I or II at subsequent nephrectomy (Group B) were included.
RESULTS
The 4-year overall (OS)/event free survival (EFS) for Group A (n = 117) patients was 90%(95%CI:83-94)/81%(CI:73-87) and for Group B (n = 32) 94%(CI:77-98)/88%(CI:70-95). The 4-year OS/EFS of patients with pathological stage III WT according to whether they received flank/abdominal radiotherapy (95 patients) or not (37 patients, 22 from UKW3 pooled with 17 patients from UKW2) were 91%(CI:83-95)/82%(CI:73-89), and 84%(CI:67-92)/78%(CI:61-89), respectively. The 4-year OS/EFS for patients having one reason to be stage III versus two or three was 92%(CI:84-96)/83%(CI:73-90) and 85%(CI:70-93)/78%(CI:61-88), respectively.
CONCLUSION
Our findings question the inclusion of biopsy or pre-operative chemotherapy as sole criterion for assigning a tumour stage III. Selected patients with pathological stage III WT can survive without radiotherapy. Whilst cautious interpretation is needed due to the post hoc nature of these analyses, further biological studies may better characterise those who could benefit from reduced therapy.

Identifiants

pubmed: 30773174
pii: S0167-8140(18)33550-3
doi: 10.1016/j.radonc.2018.10.026
pii:
doi:

Substances chimiques

Dactinomycin 1CC1JFE158
Vincristine 5J49Q6B70F
Doxorubicin 80168379AG

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-7

Subventions

Organisme : Cancer Research UK
ID : C1188/ A4614
Pays : United Kingdom

Informations de copyright

Copyright © 2018. Published by Elsevier B.V.

Auteurs

Sabine Irtan (S)

Cancer Section, Developmental Biology & Cancer Programme, UCL Great Ormond Street Institute of Child Health, University College London, UK.

Boo Messahel (B)

Pediatric Hematology-Oncology Department, Addenbrooke's Hospital, Cambridge University Hospitals, UK.

Veronica Moroz (V)

Cancer Research UK Clinical Trials Unit (CRCTU), School of Cancer Sciences, University of Birmingham, UK.

Roger E Taylor (RE)

Clinical Oncology, Swansea University, UK.

Richard Grundy (R)

Paediatric Oncology, Queen's Medical Centre, Nottingham, UK.

Anna Kelsey (A)

Department of Pathology, Royal Manchester Children's Hospital, UK.

Gordan Vujanic (G)

Department of Pathology, School of Medicine, Cardiff University, UK.

Kathy Pritchard-Jones (K)

Cancer Section, Developmental Biology & Cancer Programme, UCL Great Ormond Street Institute of Child Health, University College London, UK. Electronic address: k.pritchard-jones@ucl.ac.uk.

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Classifications MeSH