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颅面部骨肉瘤 德国-奥地利-瑞士骨肉瘤协作研究组的经验

Craniofacial osteosarcoma Experience of the cooperative German-Austrian-Swiss osteosarcoma study group.

作者信息

Jasnau Sven, Meyer Ulrich, Potratz Jenny, Jundt Gernot, Kevric Matthias, Joos Ulrich K, Jürgens Heribert, Bielack Stefan S

机构信息

Universitätsklinikum Münster, Klinik und Poliklinik für Kinder- und Jugendmedizin, Pädiatrische Hämatologie und Onkologie, Münster, Germany.

出版信息

Oral Oncol. 2008 Mar;44(3):286-94. doi: 10.1016/j.oraloncology.2007.03.001. Epub 2007 Apr 27.

Abstract

The aim of this retrospective analysis was to evaluate patient and tumor characteristics and treatment results and prognostic factors for patients with craniofacial osteosarcoma (CFOS). The COSS database was searched for patients with previously untreated, histologically confirmed craniofacial osteosarcoma with at least one follow-up examination. In a 28-year period extending from 1977 to 2004, 49 eligible patients were identified and their charts retrospectively analysed. The median age at diagnosis was 19.7 years (range: 4.6-57.2) with no gender predilection. Thirteen CFOS were second or even third primary malignancies. The jaws were the primary site in 27 patients (55% - mandible 15 (31%), maxilla 12 (24%)), while extragnathic bones were involved in 22 (45%). All 49 patients underwent surgery; in 37 (76%) combined with chemotherapy, in seven (14%) with chemotherapy and radiotherapy. Twenty-one patients (43%) received preoperative chemotherapy and the other 28 (57%) had primary surgery. A complete surgical remission was achieved in 32 patients, of whom 24 remained in local control. Actuarial five-year overall and event-free survival rates were 74% and 44%, respectively. Extragnathic site (p<.001) and documented postsurgical rest of the primary tumor (p<.001) were associated with inferior overall survival probabilities. All 24 patients who achieved and maintained local surgical control survived disease-free. Multidisciplinary treatment of CFOS within a multicenter setting resulted in long-term survival in well over two thirds of affected patients. Extragnathic sites and failure to achieve and maintain local surgical control emerged as strong negative prognostic factors.

摘要

这项回顾性分析的目的是评估颅面部骨肉瘤(CFOS)患者的患者和肿瘤特征、治疗结果及预后因素。在COSS数据库中搜索之前未经治疗、组织学确诊为颅面部骨肉瘤且至少接受过一次随访检查的患者。在1977年至2004年的28年期间,确定了49例符合条件的患者,并对其病历进行回顾性分析。诊断时的中位年龄为19.7岁(范围:4.6 - 57.2岁),无性别倾向。13例CFOS为第二或第三原发性恶性肿瘤。27例患者(55%)的原发部位在颌骨(下颌骨15例(31%),上颌骨12例(24%)),22例(45%)累及颌骨外骨骼。49例患者均接受了手术;37例(76%)联合化疗,7例(14%)联合化疗和放疗。21例患者(43%)接受了术前化疗,另外28例(57%)接受了初次手术。32例患者实现了手术完全缓解,其中24例保持局部控制。精算的五年总生存率和无事件生存率分别为74%和44%。颌骨外部位(p<0.001)和记录的原发肿瘤术后残留(p<0.001)与总体生存概率较低相关。所有实现并维持局部手术控制的24例患者均无病生存。在多中心环境下对CFOS进行多学科治疗,使超过三分之二的受影响患者获得长期生存。颌骨外部位以及未能实现并维持局部手术控制成为强有力的不良预后因素。

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