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肢体原发性非转移性小儿骨肉瘤治疗中的较高生存率。

Superior survival in treatment of primary nonmetastatic pediatric osteosarcoma of the extremity.

作者信息

Wilkins Ross M, Cullen John W, Odom Lorrie, Jamroz Brandt A, Cullen Patsy McGuire, Fink Kyle, Peck Sanford D, Stevens Sydney L, Kelly Cynthia M, Camozzi Anne B

机构信息

Institute for Limb Preservation at Presbyterian/St. Luke's Medical Center, Denver, Colorado 80210, USA.

出版信息

Ann Surg Oncol. 2003 Jun;10(5):498-507. doi: 10.1245/aso.2003.03.061.

Abstract

BACKGROUND

A protocol to treat osteosarcoma of the extremity was developed at two local institutions.

METHODS

The study involved a dose-intensified neoadjuvant protocol of intravenous doxorubicin and intra-arterial cisplatin administered repetitively until maximum angiographic response was noted. Definitive surgery was delayed until > or =90% reduction in tumor neovascularity was documented. Prospective assessment of serial arteriograms was highly accurate (94%) in predicting histological response and assisted in surgical planning. After resection, if patients were determined to be good responders (> or =90% tumor necrosis), they underwent a 4-month postoperative course with the same agents. Poor responders (<90% necrosis) were treated with alternative agents for 12 months from diagnosis. Forty-seven assessable patients with primary, high-grade, nonmetastatic osteosarcoma of the extremity were included in this analysis. The median age was 15 years (range, 7-21 years).

RESULTS

Patients underwent an average of four preoperative intra-arterial courses. Forty-three patients underwent limb-preservation procedures, and 41 had >90% tumor necrosis. With an average follow-up of 92 months (range, 20-178 months), 39 patients were continuously disease free, 3 died of disease, 1 died of other causes, and 4 have no evidence of disease 11 to 51 months after relapse (all pulmonary metastases). There were no local recurrences. Kaplan-Meier analysis demonstrated a 10-year overall survival of 92% and an event-free survival of 84%.

CONCLUSIONS

This study demonstrates excellent survival with a dose-intensified neoadjuvant protocol. Future endeavors should involve a multi-institutional randomized study comparing this approach with another multiagent intravenous neoadjuvant protocol.

摘要

背景

两家当地机构制定了一项治疗肢体骨肉瘤的方案。

方法

该研究采用了一种剂量强化的新辅助方案,即重复静脉注射阿霉素和动脉内注射顺铂,直至血管造影显示最大反应。确定性手术推迟至记录到肿瘤新生血管减少≥90%。对系列动脉造影进行前瞻性评估在预测组织学反应方面高度准确(94%),并有助于手术规划。切除术后,如果确定患者为良好反应者(肿瘤坏死≥90%),则术后4个月使用相同药物治疗。反应不佳者(坏死<90%)从诊断开始用其他药物治疗12个月。本分析纳入了47例可评估的原发性、高级别、非转移性肢体骨肉瘤患者。中位年龄为15岁(范围7 - 21岁)。

结果

患者平均接受了四次术前动脉内治疗疗程。43例患者接受了保肢手术,41例患者肿瘤坏死>90%。平均随访92个月(范围20 - 178个月),39例患者持续无病生存,3例死于疾病,1例死于其他原因,4例在复发(均为肺转移)后11至51个月无疾病证据。无局部复发。Kaplan - Meier分析显示10年总生存率为92%,无事件生存率为84%。

结论

本研究表明剂量强化新辅助方案具有出色的生存率。未来的努力应包括一项多机构随机研究,将该方法与另一种多药静脉新辅助方案进行比较。

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