Ewing Sarcoma/Primitive Neuroectodermal Tumor of the Chest Wall
2003; Lippincott Williams & Wilkins; Volume: 238; Issue: 4 Linguagem: Inglês
10.1097/01.sla.0000089857.45191.52
ISSN1528-1140
AutoresRobert C. Shamberger, Michael P. LaQuaglia, Mark C. Gebhardt, James R. Neff, Nancy J. Tarbell, Karen Marcus, Scott L. Sailer, Richard B. Womer, James S. Miser, Paul S. Dickman, Elizabeth J. Perlman, Meenakshi Devidas, Stephen B. Linda, Mark Krailo, Holcombe E. Grier, Linda Granowetter,
Tópico(s)Neuroblastoma Research and Treatments
ResumoIn Brief Objective: To establish outcome and optimal timing of local control for patients with nonmetastatic Ewing sarcoma/primitive neuroectodermal tumor (ES/PNET) of the chest wall. Methods: Patients ≤30 years of age with ES/PNET of the chest wall were entered in 2 consecutive protocols. Therapy included multiagent chemotherapy; local control was achieved by resection, radiotherapy, or both. We compared completeness of resection and disease-free survival in patients undergoing initial surgical resection versus those treated with neoadjuvant chemotherapy followed by resection, radiotherapy, or both. Patients with a positive surgical margin received radiotherapy. Results: Ninety-eight (11.3%) of 869 patients had primary tumors of the chest wall. Median follow-up was 3.47 years and 5-year event-free survival was 56% for the chest wall lesions. Ten of 20 (50%) initial resections resulted in negative margins compared with 41 of 53 (77%) negative margins with delayed resections after chemotherapy (P = 0.043). Event-free survival did not differ by timing of surgery (P = 0.69) or type of local control (P = 0.17). Initial chemotherapy decreased the percentage of patients needing radiation therapy. Seventeen of 24 patients (70.8%) with initial surgery received radiotherapy compared with 34 of 71 patients (47.9%) who started with chemotherapy (P = 0.061). If a delayed operation was performed, excluding those patients who received only radiotherapy for local control, only 25 of 62 patients needed radiotherapy (40.3%; P = 0.016). Conclusion: The likelihood of complete tumor resection with a negative microscopic margin and consequent avoidance of external beam radiation and its potential complications is increased with neoadjuvant chemotherapy and delayed resection of chest wall ES/PNET. The extent of resection and disease-free survival was assessed in patients with chest wall Ewing sarcoma/primitive neuroectodermal tumors treated in 2 consecutive studies. When compared with initial resection, neoadjuvant chemotherapy and delayed resection increased the likelihood of complete tumor resection with negative microscopic margins and avoidance of radiotherapy.
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