Prognostic impact of lymph node involvement and loss of heterozygosity of 1p or 16q in stage III favorable histology Wilms tumor: A report from Children’s Oncology Group Studies AREN03B2 and AREN0532

Author:

Evageliou Nicholas1ORCID,Renfro Lindsay A.2,Geller James3ORCID,Perlman Elizabeth4,Kalapurakal John5,Paulino Arnold6ORCID,Dix David7,Eklund Meryle J.8,Murphy Andrew J.9ORCID,Romao Rodrigo L. P.10,Ehrlich Peter F.11ORCID,Varela Carly R.121314,Vallance Kelly15,Fernandez Conrad V.16,Dome Jeffrey S.1214,Mullen Elizabeth A.17

Affiliation:

1. Division of Oncology Children’s Hospital of Philadelphia Philadelphia Pennsylvania USA

2. Division of Biostatistics University of Southern California and Children’s Oncology Group Monrovia California USA

3. Division of Oncology Cincinnati Children’s Hospital Medical Center University of Cincinnati Cincinnati Ohio USA

4. Department of Pathology and Laboratory Medicine The Ann & Robert H. Lurie Children’s Hospital of Chicago Northwestern University Chicago Illinois USA

5. Department of Radiation Oncology Robert H. Lurie Cancer Center Northwestern University Chicago Illinois USA

6. Department of Radiation Oncology MD Anderson Cancer Center Houston Texas USA

7. Division of Oncology British Columbia Children’s Hospital Vancouver British Columbia Canada

8. Department of Radiology Medical University of South Carolina Charleston South Carolina USA

9. Department of Surgery St. Jude Children’s Research Hospital Memphis Tennessee USA

10. Departments of Surgery and Urology IWK Health Dalhousie University Halifax Nova Scotia Canada

11. Section of Pediatric Surgery Department of Surgery University of Michigan Ann Arbor Michigan USA

12. Division of Oncology Children’s National Hospital Washington District of Columbia USA

13. Divisions of Pediatric Hematology and Oncology Inova Fairfax Hospital Fairfax Virginia USA

14. Department of Pediatrics George Washington University School of Medicine and Health Sciences Washington District of Columbia USA

15. Division of Hematology and Oncology Cook Children’s Hospital Fort Worth Texas USA

16. Department of Pediatrics IWK Health Centre and Dalhousie University Halifax Nova Scotia Canada

17. Dana‐Farber/Boston Children's Blood Disorders and Cancer Center Boston Massachusetts USA

Abstract

AbstractIntroductionThe prognostic impact of positive lymph nodes (LN+) and/or singular loss of heterozygosity (LOH) of 1p or 16q were assessed in children with stage III favorable histology Wilms tumor (FHWT) enrolled on AREN0532 or AREN03B2 alone.Patients and MethodsA total of 635 stage III FHWT vincristine/dactinomycin/doxorubicin (DD4A)–treated patients met inclusion criteria. Event‐free survival (EFS) and overall survival are reported overall and by LN sampling, LN status, LOH 1p, LOH 16q, and a combination of LN status and singular LOH. Patients with unknown or positive combined LOH of 1p and 16q status and AREN03B2‐only patients with unknown outcomes or treatment other than DD4A were excluded.ResultsEFS did not differ by study, supporting pooling. Lack of LN sampling (hazard ratio [HR], 2.12; p = .0037), LN positivity (HR, 2.78; p = .0002), LOH 1p (HR, 2.18; p = .0067), and LOH 16q (HR, 1.72; p = .042) were associated with worse EFS. Compared with patients with both LN– and LOH–, those with negative nodes but positive LOH 1p or 16q and those with LN+ but LOH– for 1p or 16q had significantly worse EFS (HR, 3.05 and 3.57, respectively). Patients positive for both LN and LOH had the worst EFS (HR, 6.33; overall group factor, p < .0001).ConclusionFindings confirm LN+ status as an adverse prognostic factor amplified by presence of singular LOH 1p or 16q, supporting study of intensified therapy for patients with LN+ in combination with singular LOH in a prospective clinical trial.

Funder

National Cancer Institute

St. Baldrick's Foundation

Publisher

Wiley

Subject

Cancer Research,Oncology

Reference19 articles.

1. Loss of Heterozygosity for Chromosomes 1p and 16q Is an Adverse Prognostic Factor in Favorable-Histology Wilms Tumor: A Report From the National Wilms Tumor Study Group

2. Vallance K RefroL EvageliouN et al.Impact of biomarkers on outcome in stage I and II low risk favorable histology Wilms tumors. A report From the Children’s Oncology Group AREN03B2 Protocol. oral abstract SIOP World Congress Barcelona 2022.

3. Loss of heterozygosity on chromosome 16q increases relapse risk in Wilms’ tumor: a meta-analysis

4. Biomarkers for Wilms Tumor: A Systematic Review

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