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骨肉瘤:德国骨肉瘤协作组(COSS)的经验

Osteosarcoma: the COSS experience.

作者信息

Bielack Stefan, Jürgens Herbert, Jundt Gernot, Kevric Matthias, Kühne Thomas, Reichardt Peter, Zoubek Andreas, Werner Mathias, Winkelmann Winfried, Kotz Rainer

机构信息

Pädiatrie 5 (Onkologie, Hämatologie,Immunologie), Klinikum Stuttgart, Zentrum für Kinder- und Jugendmedizin-Olgahospital, Bismarckstr. 8, D-70176, Stuttgart, Germany.

出版信息

Cancer Treat Res. 2009;152:289-308. doi: 10.1007/978-1-4419-0284-9_15.

Abstract

COSS, the interdisciplinary Cooperative German-Austrian-Swiss Osteosarcoma Study Group, was founded in 1977 and has since registered some 3,500 bone sarcoma patients from over 200 institutions. For the purpose of the Pediatric and Adolescent Osteosarcoma Conference in Houston, March 2008, the outcomes of 2,464 consecutive patients with high-grade central osteosarcoma, who had been diagnosed between 1980 and 2005 and had been treated on neoadjuvant COSS protocols, were reviewed. Intended treatment had included surgery and multidrug chemotherapy, with high-dose methotrexate, doxorubicin, cisplatin, and ifosfamide being used in most protocols. After a median follow-up of 7.31 years for 1,654 survivors, 5- and 10-year survival estimates were 0.748/0.695 for 2,017 patients with localized extremity tumors and 0.369/0.317 for 444 patients with axial tumors or/and primary metastases, respectively. Tumor response to preoperative chemotherapy was of independent prognostic significance. Over the years, there was a major shift from amputation towards limb-salvage. This development was least evident for patients below the age of 10. While survival expectancies improved from the first to the second half of the recruitment period, no further improvement was evident within the latter period. In the manuscript, the results described above are discussed based on the findings of the previous analyses of our group.

摘要

COSS,即跨学科的德奥瑞骨肉瘤合作研究组,成立于1977年,自那时起已登记了来自200多家机构的约3500例骨肉瘤患者。为了2008年3月在休斯敦召开的儿童和青少年骨肉瘤会议,回顾了1980年至2005年间诊断出的2464例连续的高级别中央型骨肉瘤患者的治疗结果,这些患者接受了新辅助COSS方案治疗。预期治疗包括手术和多药化疗,大多数方案中使用了大剂量甲氨蝶呤、阿霉素、顺铂和异环磷酰胺。1654名幸存者的中位随访时间为7.31年,2017例局限性肢体肿瘤患者的5年和10年生存率估计分别为0.748/0.695,444例轴向肿瘤或/和原发性转移患者的5年和10年生存率估计分别为0.369/0.317。肿瘤对术前化疗的反应具有独立的预后意义。多年来,治疗方式从截肢向保肢发生了重大转变。这种转变在10岁以下的患者中最不明显。虽然从招募期的前半段到后半段生存率有所提高,但在后半段期间没有明显进一步改善。在本手稿中,基于我们组先前分析的结果对上述结果进行了讨论。

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