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蒽环类药物联合顺铂化疗所致毒性与局限性肢体骨肉瘤患者生存改善相关:来自欧洲骨肉瘤协作组的报告。

Presence of chemotherapy-induced toxicity predicts improved survival in patients with localised extremity osteosarcoma treated with doxorubicin and cisplatin: a report from the European Osteosarcoma Intergroup.

机构信息

Department of Oncology, University College Hospital, London, UK.

出版信息

Eur J Cancer. 2012 Mar;48(5):703-12. doi: 10.1016/j.ejca.2011.09.012. Epub 2011 Oct 27.

Abstract

AIM

Chemotherapy-induced toxicity is an independent prognostic indicator in several cancers. We aimed to determine whether toxicity was related to survival and histological response in high-grade localised extremity osteosarcoma. We undertook a retrospective analysis of patients treated within three consecutive randomised controlled trials (RCTs) of the European Osteosarcoma Intergroup.

METHODS

Between 1982 and 2002, 533 patients were randomised to six cycles of doxorubicin 75 mg/m(2) and cisplatin 100 mg/m(2). Toxicity data were collected prospectively and graded according to the World Health Organisation (WHO) criteria. Standard univariate and multivariate models were constructed to examine the relationship between reported toxicity, survival, and histological response.

RESULTS

Five- and 10-year overall survival was 57% (95% confidence interval (CI) 52-61%) and 53% (49-58%), respectively. Grades 3-4 oral mucositis (hazard ratio (HR) 0.51, 95% CI 0.29-0.91), grades 1-2 nausea/vomiting (HR 0.37, 95% CI 0.16-0.85), grades 1-2 thrombocytopenia (HR 0.49, 95% CI 0.27-0.87), good histological response (HR 0.42, 95% CI 0.27-0.65), and distal tumour site (HR 0.45, 95% CI 0.28-0.71) were associated with improved survival in multivariate analysis. The only factors that were independently associated with histological response were older age (odds ratio (OR) 0.18, 95% CI 0.04-0.72) and chondroblastic tumour (OR 0.28, 95% CI 0.10-0.77), both being associated with a significantly lower chance of achieving a good response.

CONCLUSION

Chemotherapy-induced toxicity predicts survival in patients with localised extremity osteosarcoma. Investigation of the pharmacogenomic mechanisms of constitutional chemosensitivity underlying these observations will present opportunities for personalising treatment and could lead to improved outcomes.

摘要

目的

化疗引起的毒性是几种癌症的独立预后指标。我们旨在确定毒性是否与高级局部肢体骨肉瘤的生存和组织学反应有关。我们对欧洲骨肉瘤组连续三项随机对照试验(RCT)中治疗的患者进行了回顾性分析。

方法

1982 年至 2002 年间,533 名患者被随机分配至六周期阿霉素 75mg/m²和顺铂 100mg/m²。毒性数据是前瞻性收集的,并根据世界卫生组织(WHO)标准进行分级。构建了标准的单变量和多变量模型,以检查报告的毒性、生存和组织学反应之间的关系。

结果

5 年和 10 年总生存率分别为 57%(95%置信区间(CI)52-61%)和 53%(49-58%)。3-4 级口腔粘膜炎(危险比(HR)0.51,95%CI 0.29-0.91)、1-2 级恶心/呕吐(HR 0.37,95%CI 0.16-0.85)、1-2 级血小板减少症(HR 0.49,95%CI 0.27-0.87)、良好的组织学反应(HR 0.42,95%CI 0.27-0.65)和肿瘤部位较远端(HR 0.45,95%CI 0.28-0.71)与多变量分析中的生存改善相关。唯一与组织学反应独立相关的因素是年龄较大(比值比(OR)0.18,95%CI 0.04-0.72)和软骨母细胞瘤(OR 0.28,95%CI 0.10-0.77),两者均与实现良好反应的机会显著降低有关。

结论

局部肢体骨肉瘤患者的化疗诱导毒性可预测生存。对这些观察结果所涉及的体质化疗敏感性的遗传机制的研究将为治疗个体化提供机会,并可能改善预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca93/3657154/e6c2e08ad7bf/gr1.jpg

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