Results for patients with sarcoma not otherwise specified and other diagnoses than Ewing sarcoma treated according to the Euro-EWING 99 trial

被引:4
|
作者
Frank, Judith Amalie [1 ]
Ranft, Andreas [1 ]
Paulussen, Michael [2 ]
Juergens, Heribert [1 ]
Kruseova, Jarmila [3 ]
Bauer, Sebastian [4 ]
Niggli, Felix [5 ]
Reichardt, Peter [6 ]
Dirksen, Uta [1 ]
机构
[1] Westfalian Wilhelms Univ, Univ Hosp Muenster, Dept Pediat Hematol & Oncol, Munster, Germany
[2] Univ Witten Herdecke, Vest Kinder & Jugendklin, Datteln, Germany
[3] Univ Hosp Motol, Dept Pediat Hematol & Oncol, Prague, Czech Republic
[4] Univ Klinikum Essen, West German Canc Ctr, Sarcoma Ctr, Essen, Germany
[5] Univ Childrens Hosp Zurich, Dept Oncol, Zurich, Switzerland
[6] HELIOS Klinikum Berlin Buch, Dept Interdisciplinary Oncol, Berlin, Germany
关键词
bone; Ewing tumors; osteosarcoma; sarcomas; sarcoma NOS; soft tissue sarcoma; tumors; RHABDOMYOSARCOMA-STUDY-IV; FRANCAISE-DES-CANCERS; ROUND-CELL SARCOMAS; PROGNOSTIC-FACTORS; NONMETASTATIC RHABDOMYOSARCOMA; UNDIFFERENTIATED SARCOMAS; STANDARD CHEMOTHERAPY; INTERNATIONAL SOCIETY; SOFT-TISSUES; TUMORS;
D O I
10.1002/pbc.26524
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundEuro-EWING 99 trial of the European Ewing tumor Working Initiative of National Groups (EE99) was an international phase III study in patients with Ewing sarcoma. The German Society of Pediatric Oncology and Hematology (GPOH) data center registered and followed patients with other diagnoses than Ewing sarcoma who were treated according to the EE99 protocol in an additional non-Ewing database. ProcedureData of 27 patients with other diagnoses than Ewing sarcoma treated according to the EE99 protocol were analyzed. Patients had miscellaneous histologic diagnoses, the majority were diagnosed with sarcoma not otherwise specified (NOS) arising in bone and soft tissue (63%). ResultsThe median age at diagnosis was 16.9 years (range 4.5-41.4). Localized disease was diagnosed in 61.5% of the patients and 38.5% had distant metastases at time of primary diagnosis. The median follow-up time was 3.7 years (range 0.5-9.5). Patients with localized disease showed a 3-year event-free survival (EFS) of 68%, compared to 3-year EFS of 20% in patients with metastases (P = 0.042). Three-year EFS for patients with sarcoma NOS was 52%, patients with localized and metastatic disease showed 3-year EFS of 66 and 20%, respectively. ConclusionEFS in patients with other diagnoses than Ewing sarcoma treated according to EE99 was significantly higher in patients with localized than metastatic disease. Sarcomas of soft tissue and bone that cannot be classified to current diagnostic categories constitute a therapeutic challenge.
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页数:8
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