Treatment of stage I anaplastic Wilms' tumour: a report from the Children's Oncology Group AREN0321 study.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
09 2019
Historique:
received: 27 01 2019
revised: 30 03 2019
accepted: 22 05 2019
pubmed: 22 7 2019
medline: 9 6 2020
entrez: 21 7 2019
Statut: ppublish

Résumé

In the fifth National Wilms Tumor Study (NWTS-5), the 4-year event-free survival (EFS) and overall survival (OS) estimates for 29 patients with stage I focal (n = 10) or diffuse (n = 19) anaplastic Wilms' tumour (AWT) treated with vincristine and dactinomycin without flank radiation were 69.5% and 82.6%, respectively. The Children's Oncology Group AREN0321 study evaluated whether adding doxorubicin and flank radiation improves survival for these patients. Tumour histology and stage were confirmed by real-time central pathology, surgery and radiology review. The patients received 25 weeks of vincristine, dactinomycin and doxorubicin (cumulative dose 150 mg/m Eighteen patients with stage I AWT (8 focal and 10 diffuse) were enrolled on AREN0321. With a median follow-up of 4.6 years, the 4-year EFS and OS were 100%. One patient with diffuse AWT had pulmonary relapse 4.12 years after diagnosis. In the 112 patients with stage I AWT treated in NWTSs 1-5 and AREN0321, the EFS was significantly improved with doxorubicin treatment (p = 0.01; 4-year EFS: 97.2% [95% confidence interval {CI}: 91.3-100] vs. 77.5% [95% CI: 67.6-87.4]) but not by flank radiation (p = 0.15). Treatment of stage I AWT with vincristine, dactinomycin, doxorubicin and flank radiation in AREN0321 yielded excellent survival outcomes. Retrospective analysis of AREN0321 and NWTS patients suggests that doxorubicin had a greater contribution to the excellent outcomes than radiation.

Sections du résumé

BACKGROUND
In the fifth National Wilms Tumor Study (NWTS-5), the 4-year event-free survival (EFS) and overall survival (OS) estimates for 29 patients with stage I focal (n = 10) or diffuse (n = 19) anaplastic Wilms' tumour (AWT) treated with vincristine and dactinomycin without flank radiation were 69.5% and 82.6%, respectively. The Children's Oncology Group AREN0321 study evaluated whether adding doxorubicin and flank radiation improves survival for these patients.
PATIENTS AND METHODS
Tumour histology and stage were confirmed by real-time central pathology, surgery and radiology review. The patients received 25 weeks of vincristine, dactinomycin and doxorubicin (cumulative dose 150 mg/m
RESULTS
Eighteen patients with stage I AWT (8 focal and 10 diffuse) were enrolled on AREN0321. With a median follow-up of 4.6 years, the 4-year EFS and OS were 100%. One patient with diffuse AWT had pulmonary relapse 4.12 years after diagnosis. In the 112 patients with stage I AWT treated in NWTSs 1-5 and AREN0321, the EFS was significantly improved with doxorubicin treatment (p = 0.01; 4-year EFS: 97.2% [95% confidence interval {CI}: 91.3-100] vs. 77.5% [95% CI: 67.6-87.4]) but not by flank radiation (p = 0.15).
CONCLUSIONS
Treatment of stage I AWT with vincristine, dactinomycin, doxorubicin and flank radiation in AREN0321 yielded excellent survival outcomes. Retrospective analysis of AREN0321 and NWTS patients suggests that doxorubicin had a greater contribution to the excellent outcomes than radiation.

Identifiants

pubmed: 31325873
pii: S0959-8049(19)30361-2
doi: 10.1016/j.ejca.2019.05.033
pmc: PMC6690766
mid: NIHMS1535010
pii:
doi:

Substances chimiques

Dactinomycin 1CC1JFE158
Vincristine 5J49Q6B70F
Doxorubicin 80168379AG

Types de publication

Comparative Study Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

58-66

Subventions

Organisme : NCI NIH HHS
ID : U10 CA098413
Pays : United States
Organisme : NCI NIH HHS
ID : U24 CA114766
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA098543
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180899
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180886
Pays : United States

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

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Auteurs

Najat C Daw (NC)

Division of Pediatrics, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd Unit 87, Houston, TX 77030-4009, USA. Electronic address: ndaw@mdanderson.org.

Yueh-Yun Chi (YY)

Department of Biostatistics, University of Florida, 6011 NW 1st Place Suite 10, Gainesville, FL 32607, USA. Electronic address: ychi@cog.ufl.edu.

Yeonil Kim (Y)

Department of Biostatistics, University of Florida, 6011 NW 1st Place Suite 10, Gainesville, FL 32607, USA.

Elizabeth A Mullen (EA)

Department of Pediatric Hematology/Oncology, Dana-Farber/Harvard Cancer Center, Dana Farber Cancer Institute, 450 Brookline Ave. Office#: SW360A, Boston, MA 02215-5450, USA. Electronic address: elizabeth_mullen@dfci.harvard.edu.

John A Kalapurakal (JA)

Department of Radiation Oncology, Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern Memorial Hospital, 25i East Huron Street Suite#L178, Chicago, IL 60611, USA. Electronic address: j-kalapurakal@northwestern.edu.

Jing Tian (J)

Children's Oncology Group Data Center, Statistics Data Center, 6011 NW 1st Place Suite 10, Gainesville, FL 32607, USA. Electronic address: jtian@cog.ufl.edu.

Geetika Khanna (G)

Mallinckrodt Institute of Radiology, Washington University School of Medicine, 510 S. Kingshighway, Box 8131, St. Louis, MO 63110, USA. Electronic address: khannag@wustl.edu.

James I Geller (JI)

Division of Oncology, Cincinnati Children's Hospital Medical Center, University of Cincinnati, 3333 Burnet Avenue MLC 7015, Cincinnati, OH 45229, USA. Electronic address: james.geller@cchmc.org.

Elizabeth J Perlman (EJ)

Department of Pathology, Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, 225 East Chicago Avenue, Chicago, IL 60611, USA. Electronic address: eperlman@luriechildrens.org.

Peter F Ehrlich (PF)

Department of Pediatric Surgery, University of Michigan, 4-945 C.S. Mott Children's Hospital SPC 4211, 1500 E. Medical Center Drive, Ann Arbor, MI 48109-4211, USA. Electronic address: pehrlich@med.umich.edu.

Anne B Warwick (AB)

Department of Pediatrics, F. Edward Hébert School of Medicine, Uniformed Services University, 4301 Jones Bridge Road, Bethesda, MD 20814, USA. Electronic address: anne.warwick@usuhs.edu.

Paul E Grundy (PE)

Department of Pediatrics, University of Alberta Hospital, WMC 4E2.28, 8440-112 Street, Edmonton, Alberta T6G 2B7, Canada. Electronic address: paul.e.grundy@ahs.ca.

Conrad V Fernandez (CV)

Departments of Pediatrics and Bioethics, IWK Health Centre, Dalhousie University and the IWK Health Centre, 5850 University Avenue, Halifax, Nova Scotia B3K 6R8, Canada. Electronic address: conrad.fernandez@iwk.nshealth.ca.

Jeffrey S Dome (JS)

Division of Oncology, Children's National Medical Center, Center for Cancer and Blood Disorders, George Washington University School of Medicine and Health Sciences, 111 Michigan Avenue NW, Washington, DC 20010, USA. Electronic address: jdome@childrensnational.org.

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