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1.
Ann Surg Oncol ; 20(11): 3384-90, 2013 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-23838914

RESUMO

BACKGROUND: Pediatric desmoid tumors (PDTs) represent a group of rare, distinct lesions. While sparse, available literature suggests that PDT are particularly aggressive and difficult to control when compared with their adult counterpart. METHODS: A retrospective review identified 39 patients who underwent treatment of PDT at St. Jude Children's Research Hospital over a 12-year period. Clinicopathologic and treatment characteristics were analyzed to identify predictors of outcome. RESULT: A total of 39 patients were treated during the study period, with a total number of 67 resections. Median age was 12.2 years; 49 % of patients were male, and 51 % were female. Median tumor size was 9.8 cm. PDT most commonly arose in the extremities (40 %), thorax (23 %), head and neck (21 %), and trunk (16 %). Also, 18 % of resections had negative margins (R0), 48 % were microscopic positive (R1), and 30 % were macroscopic positive (R2). The 1- and 5-year recurrence-free survival (RFS) was 97.1 and 73.1 %, respectively. Factors associated with worse RFS were patient age >12 years (HR = 5.08, p = 0.038) and tumor size >5 cm (HR = 1.22, p = 0.0597). Margin status did not affect RFS. Selective use of radiation therapy appeared to improve RFS. CONCLUSIONS: Our study suggests that margin status alone at the time of extirpation is not a predictor of ultimate cure or likelihood of recurrence. Many patients received adjuvant therapy, with benefits suggested after analysis. For patients with PDT, surgical extirpation should not come at the expense of functional preservation, as overall survival is excellent.


Assuntos
Fibromatose Agressiva/mortalidade , Fibromatose Agressiva/cirurgia , Recidiva Local de Neoplasia/mortalidade , Recidiva Local de Neoplasia/cirurgia , Adolescente , Adulto , Criança , Pré-Escolar , Feminino , Fibromatose Agressiva/patologia , Seguimentos , Humanos , Lactente , Metástase Linfática , Masculino , Recidiva Local de Neoplasia/patologia , Estadiamento de Neoplasias , Prognóstico , Estudos Retrospectivos , Taxa de Sobrevida , Fatores de Tempo , Adulto Jovem
2.
Int J Radiat Oncol Biol Phys ; 101(4): 860-874, 2018 07 15.
Artigo em Inglês | MEDLINE | ID: mdl-29976498

RESUMO

PURPOSE: Our aim was to review the advances in radiation therapy for the management of pediatric cancers made by the Children's Oncology Group (COG) radiation oncology discipline since its inception in 2000. METHODS AND MATERIALS: The various radiation oncology disease site leaders reviewed the contributions and advances in pediatric oncology made through the work of the COG. They have presented outcomes of relevant studies and summarized current treatment policies developed by consensus from experts in the field. RESULTS: The indications and techniques for pediatric radiation therapy have evolved considerably over the years for virtually all pediatric tumor types, resulting in improved cure rates together with the potential for decreased treatment-related morbidity and mortality. CONCLUSIONS: The COG radiation oncology discipline has made significant contributions toward the treatment of childhood cancer. Our discipline is committed to continuing research to refine and modernize the use of radiation therapy in current and future protocols with the goal of further improving the cure rates and quality of life of children with cancer.


Assuntos
Neoplasias/radioterapia , Radioterapia (Especialidade)/organização & administração , Neoplasias Ósseas/radioterapia , Neoplasias do Sistema Nervoso Central/radioterapia , Criança , Doença de Hodgkin/radioterapia , Humanos , Cooperação Internacional , Neoplasias Renais/radioterapia , Leucemia/radioterapia , Neuroblastoma/radioterapia , Terapia com Prótons , Radioterapia (Especialidade)/educação , Radioterapia (Especialidade)/tendências , Doenças Raras/radioterapia , Sarcoma/radioterapia , Sarcoma de Ewing/radioterapia , Fatores de Tempo
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