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Treatment and outcomes of clear cell sarcoma of the kidney: A report from the Children's Oncology Group studies AREN0321 and AREN03B2.
Benedetti, Daniel J; Renfro, Lindsay A; Tfirn, Ian; Daw, Najat C; Kalapurakal, John A; Ehrlich, Peter F; Khanna, Geetika; Perlman, Elizabeth; Warwick, Anne; Gow, Kenneth W; Paulino, Arnold C; Seibel, Nita L; Grundy, Paul; Fernandez, Conrad V; Geller, James I; Mullen, Elizabeth A; Dome, Jeffrey S.
Afiliação
  • Benedetti DJ; Division of Hematology/Oncology, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Renfro LA; Division of Biostatistics, University of Southern California, Los Angeles, California, USA.
  • Tfirn I; Children's Oncology Group, Monrovia, California, USA.
  • Daw NC; Children's Oncology Group, Monrovia, California, USA.
  • Kalapurakal JA; Division of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Ehrlich PF; Department of Radiation Oncology, Northwestern University, Chicago, Illinois, USA.
  • Khanna G; Section of Pediatric Surgery, University of Michigan, Ann Arbor, Michigan, USA.
  • Perlman E; Department of Radiology and Imaging Sciences, Emory University, Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
  • Warwick A; 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.
  • Gow KW; Department of Pediatrics, F. Edward Hébert School of Medicine, Uniformed Services University, Bethesda, Maryland, USA.
  • Paulino AC; Division of Pediatric General and Thoracic Surgery, Seattle Children's Hospital, University of Washington, Seattle, Washington, USA.
  • Seibel NL; Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Grundy P; Division of Cancer Treatment and Diagnosis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
  • Fernandez CV; Division of Immunology, Hematology, Oncology, Palliative Care, and Environmental Interactions, University of Alberta, Edmonton, Alberta, Canada.
  • Geller JI; Division of Pediatric Hematology/Oncology, IWK Health Centre, Dalhousie University, Halifax, Nova Scotia, Canada.
  • Mullen EA; Division of Oncology, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio, USA.
  • Dome JS; Department of Pediatric Hematology/Oncology, Dana-Farber Cancer Institute/Boston Children's Hospital, Boston, Massachusetts, USA.
Cancer ; 130(13): 2361-2371, 2024 Jul 01.
Article em En | MEDLINE | ID: mdl-38396300
ABSTRACT

BACKGROUND:

On 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.

METHODS:

Four-year EFS was analyzed for patients enrolled on AREN0321 and on those enrolled on AREN03B2 who received AREN0321 stage-appropriate chemotherapy.

RESULTS:

Eighty-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.

CONCLUSIONS:

Patients 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).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vincristina / Protocolos de Quimioterapia Combinada Antineoplásica / Sarcoma de Células Claras / Neoplasias Renais Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vincristina / Protocolos de Quimioterapia Combinada Antineoplásica / Sarcoma de Células Claras / Neoplasias Renais Idioma: En Ano de publicação: 2024 Tipo de documento: Article