Primary mediastinal germ cell tumors in children and adolescents: Results of the German cooperative protocols MAKEI 83/86, 89, and 96

Citation
Dt. Schneider et al., Primary mediastinal germ cell tumors in children and adolescents: Results of the German cooperative protocols MAKEI 83/86, 89, and 96, J CL ONCOL, 18(4), 2000, pp. 832-839
Citations number
18
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
JOURNAL OF CLINICAL ONCOLOGY
ISSN journal
0732183X → ACNP
Volume
18
Issue
4
Year of publication
2000
Pages
832 - 839
Database
ISI
SICI code
0732-183X(200002)18:4<832:PMGCTI>2.0.ZU;2-A
Abstract
Purpose: To evaluate children and adolescents with primary mediastinal tera toma and malignant germ cell tumors (GCTs). Patients and Methods Forty-seven patients from the German nontesticular GCT studies were analyzed (median age, 2.5 years; range, neonate to 17 years). Teratoma (n = 21) were resected, and no adjuvant treatment was given. Mali gnant GCTs (n = 26) were treated with cisplatin-based chemotherapy and rese ction. Three of 26 patients underwent radiotherapy. Results: In all patients with teratoma, tumor markers were normal. Surgery of teratoma was complete in 17 of 21 patients and microscopically incomplet e in four of 21 patients, and we observed no relapse after a median follow- up of 29 months. In 23 of 26 patients with malignant GCTs, alpha-fetoprotei n and/or beta-human chorionic gonadotropin were elevated. Twelve of 26 pati ents received adjuvant chemotherapy after initial resection, which was comp lete in six of 12 patients, whereas delayed resection after preoperative ch emotherapy was complete in 10 of 11 patients (P = .03). Four of six patient s underwent second-look thoracotomy after incomplete primary surgery. Three of 26 patients did not undergo tumor resection, The final completeness of resection was the strongest prognostic indicator (event-free survival [EFS] , 0.94 +/- 0.06 v 0.42 +/- 0.33; P < .002). Local stage and distant metasta ses were not prognostically significant at the .05 level. For all malignant GCTs, the 5-year survival rate was 0.87 +/- 0.05 (median follow-up, 51 mon ths), with an EFS of 0.83 +/- 0.05. Conclusion: The prognosis of mediastinal teratoma is excellent after comple te or microscopically incomplete resection. In children with malignant GCT, the prognosis is favorable with a therapeutic strategy of delayed resectio n after preoperative chemotherapy. In most children, the diagnosis can be b ased on elevated tumor markers and imaging. Biopsy is indicated in nonsecre ting GCT. (C) 2000 by American Society of Clinical Oncology.