Treatment and outcomes of clear cell sarcoma of the kidney: A report from the Children's Oncology Group studies AREN0321 and AREN03B2

Author:

Benedetti Daniel J.1ORCID,Renfro Lindsay A.23,Tfirn Ian3,Daw Najat C.4,Kalapurakal John A.5,Ehrlich Peter F.6ORCID,Khanna Geetika7,Perlman Elizabeth8,Warwick Anne9,Gow Kenneth W.10,Paulino Arnold C.11ORCID,Seibel Nita L.12ORCID,Grundy Paul13ORCID,Fernandez Conrad V.14,Geller James I.15ORCID,Mullen Elizabeth A.16,Dome Jeffrey S.17

Affiliation:

1. Division of Hematology/Oncology Department of Pediatrics Vanderbilt University Medical Center Nashville Tennessee USA

2. Division of Biostatistics University of Southern California Los Angeles California USA

3. Children’s Oncology Group Monrovia California USA

4. Division of Pediatrics The University of Texas MD Anderson Cancer Center Houston Texas USA

5. Department of Radiation Oncology Northwestern University Chicago Illinois USA

6. Section of Pediatric Surgery University of Michigan Ann Arbor Michigan USA

7. Department of Radiology and Imaging Sciences Emory University Children’s Healthcare of Atlanta Atlanta Georgia USA

8. Department of Pathology and Laboratory Medicine Ann and Robert H. Lurie Children's Hospital of Chicago Northwestern University Feinberg School of Medicine Chicago Illinois USA

9. Department of Pediatrics F. Edward Hébert School of Medicine Uniformed Services University Bethesda Maryland USA

10. Division of Pediatric General and Thoracic Surgery Seattle Children's Hospital University of Washington Seattle Washington USA

11. Department of Radiation Oncology The University of Texas MD Anderson Cancer Center Houston Texas USA

12. Division of Cancer Treatment and Diagnosis National Cancer Institute National Institutes of Health Bethesda Maryland USA

13. Division of Immunology, Hematology, Oncology, Palliative Care, and Environmental Interactions University of Alberta Edmonton Alberta Canada

14. Division of Pediatric Hematology/Oncology IWK Health Centre Dalhousie University Halifax Nova Scotia Canada

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

16. Department of Pediatric Hematology/Oncology Dana‐Farber Cancer Institute/Boston Children’s Hospital Boston Massachusetts USA

17. Division of Oncology and Department of Pediatrics Children's National Hospital and the George Washington University School of Medicine and Health Sciences Washington District of Columbia USA

Abstract

AbstractBackgroundOn the fifth National Wilms Tumor Study, treatment for clear cell sarcoma of the kidney (CCSK) included combined vincristine, doxorubicin, cyclophosphamide, and etoposide (regimen I) plus radiation therapy (RT), yielding 5‐year event‐free survival (EFS) rates of 100%, 88%, 73%, and 29% for patients who had with stage I, II, III, and IV disease, respectively. In the Children’s Oncology Group study AREN0321 of risk‐adapted therapy, RT was omitted for stage I disease if lymph nodes were sampled, and carboplatin was added for stage IV disease (regimen UH‐1). Patients who had stage II/III disease received regimen I with RT.MethodsFour‐year EFS was analyzed for patients enrolled on AREN0321 and on those enrolled on AREN03B2 who received AREN0321 stage‐appropriate chemotherapy.ResultsEighty‐two patients with CCSK enrolled on AREN0321, 50 enrolled on AREN03B2 only. The 4‐year EFS rate was 82.7% (95% confidence interval [CI], 74.8%–91.4%) for AREN0321 and 89.6% (95% CI, 81.3%–98.7%) for AREN03B2 only (p = .28). When combining studies, the 4‐year EFS rates for patients who had stage I (n = 10), II (n = 47), III (n = 65), and IV (n = 10) disease were 90% (95% CI, 73.2%–100.0%), 93.4% (95% CI, 86.4%–100.0%), 82.8% (95% CI, 74.1%–92.6%), and 58.3% (95% CI, 34%–100.0%), respectively. There were no local recurrences among seven patients with stage I disease who were treated without RT. One stage I recurrence occurred in the brain, which was the most common site of relapse overall. Among patients with local stage III tumors, neither initial procedure type, margin status, nor lymph node involvement were prognostic.ConclusionsPatients with stage I CCSK had excellent outcomes without local recurrences when treated without RT. Patients with stage IV disease appeared to benefit from a carboplatin‐containing regimen, although their outcomes remained unsatisfactory. Further research is needed to improve outcomes for patients with advanced‐stage disease (ClinicalTrials.gov identifiers NCT00335556 and NCT00898365).

Publisher

Wiley

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1. Current surgical approaches to pediatric renal tumors;Pediatric Blood & Cancer;2024-05-29

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