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骨肉瘤:回顾过去,展望未来。美国的经验。

Osteosarcoma: review of the past, impact on the future. The American experience.

作者信息

Jaffe Norman

机构信息

Children's Cancer Hospital, University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Unit #87, Houston, TX 77030-4009, USA.

出版信息

Cancer Treat Res. 2009;152:239-62. doi: 10.1007/978-1-4419-0284-9_12.

Abstract

Major advances have been achieved in the treatment of osteosarcoma with the discovery of several chemotherapeutic agents that were active in the disease. These agents comprise high-dose methotrexate with leucovorin rescue, Adriamycin, cisplatin, ifosfamide and cyclophosphamide. The agents were integrated into various regimens and administered in an effort to destroy silent pulmonary micrometastases which are considered to be present in at least 80% of patients at the time of diagnosis. Their efficacy in achieving this goal was realized and their use was further extended to the application of preoperative (neoadjuvant) chemotherapy to destroy the primary tumor and achieve safe surgical resections. Disease free survival was escalated from <20% prior to the introduction of effective chemotherapy to 55-75% and overall survival to 85%. Further, the opportunity to perform limb salvage was expanded to 80% of patients. Of interest also was an attempt in one series to treat the primary tumor exclusively with chemotherapy, and abrogation of surgery. Adding to these advances, varieties of subsequently discovered agents are currently undergoing investigations in patients who have relapsed and/or failed conventional therapy. The agents include Gemcitabine, Docetaxel, novel antifolate compounds, and a liposome formulation of adriamycin (Doxil). A biological agent, muramyl tripeptide phosphatidyl ethanolamine (MTPPE) was also recently investigated in a 2x2 factorial design to determine its efficacy in combination with chemotherapy (methotrexate, cisplatin, Adriamycin and ifosfamide).In circumstances where the tumor was considered inoperable, chemotherapy and radiotherapy were advocated for local control. High dose methotrexate, Adriamycin and cisplatin and Gemcitabine interact with radiation therapy and potentiate its therapeutic effect. This combination is also particularly useful in palliation. Occasionally, the combination of radiation and chemotherapy may render a tumor suitable for surgical ablation. Samarium153, a radio active agent, is also used as palliative therapy for bone metastases.However, despite the advances achieved with the multidisciplinary application of chemotherapy, radiotherapy and surgical ablation of the primary tumor over the past 3(1/2) decades, the improved cure rate reported initially has not altered. Particularly vexing is the problem of rescuing patients who develop pulmonary metastases after receiving seemingly effective multidisciplinary treatment. Approximately 15-25% of such patients only are rendered free of disease with the reintroduction of chemotherapy and resection of metastases. Extrapulmonary metastases and multifocal osteosarcoma also constitute a major problem. The arsenal of available agents to treat such patients has not made any substantial impact in improving their survival. New chemotherapeutic agents are urgently required to improve treatment and outcome. Additional strategies to be considered are targeted tumor therapy, anti tumor angiogenesis, biotherapy and therapy based upon molecular profiles. This communication outlines sequential discoveries in the chemotherapeutic research of osteosarcoma in the United States of America. It also describes the principles regulating the therapeutic application of the regimens and considers the impact of their results on the conduct in the design of future investigations and treatment.

摘要

随着几种对骨肉瘤有效的化疗药物的发现,骨肉瘤治疗取得了重大进展。这些药物包括大剂量甲氨蝶呤加亚叶酸解救、阿霉素、顺铂、异环磷酰胺和环磷酰胺。这些药物被整合到各种治疗方案中,用于破坏隐匿性肺微转移灶,据认为在诊断时至少80%的患者体内存在这种微转移灶。它们在实现这一目标方面的疗效得到了认可,其应用进一步扩展到术前(新辅助)化疗,以破坏原发性肿瘤并实现安全的手术切除。无病生存率从有效化疗引入前的<20%提高到了55 - 75%,总生存率提高到了85%。此外,保肢手术的机会扩大到了80%的患者。同样值得关注的是,在一个系列研究中尝试仅用化疗治疗原发性肿瘤并取消手术。除了这些进展外,目前正在对复发和/或传统治疗失败的患者进行多种后续发现的药物的研究。这些药物包括吉西他滨、多西他赛、新型抗叶酸化合物以及阿霉素脂质体制剂(多美素)。一种生物制剂,胞壁酰三肽磷脂酰乙醇胺(MTPPE),最近也在一项2×2析因设计中进行了研究,以确定其与化疗(甲氨蝶呤、顺铂、阿霉素和异环磷酰胺)联合使用的疗效。在肿瘤被认为无法手术切除的情况下,主张采用化疗和放疗进行局部控制。大剂量甲氨蝶呤、阿霉素和顺铂以及吉西他滨与放射治疗相互作用并增强其治疗效果。这种联合在缓解症状方面也特别有用。偶尔,放疗和化疗的联合可能使肿瘤适合手术切除。钐153,一种放射性药物,也用作骨转移的姑息治疗。然而,尽管在过去3(1/2)十年中通过化疗、放疗和原发性肿瘤手术切除的多学科应用取得了进展,但最初报道的治愈率提高并未改变。特别棘手的问题是挽救那些在接受看似有效的多学科治疗后出现肺转移的患者。这类患者中只有约15 - 25%通过再次引入化疗和转移灶切除实现无病生存。肺外转移和多灶性骨肉瘤也构成一个主要问题。现有的治疗这类患者的药物库在改善他们的生存率方面没有产生任何实质性影响。迫切需要新的化疗药物来改善治疗和预后。需要考虑的其他策略包括靶向肿瘤治疗、抗肿瘤血管生成、生物治疗以及基于分子特征的治疗。本通讯概述了美国骨肉瘤化疗研究中的一系列发现。它还描述了治疗方案应用的原则,并考虑了其结果对未来研究设计和治疗实施的影响。

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