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

被引:46
作者
McTiernan, Anne [1 ]
Jinks, Rachel C. [2 ]
Sydes, Matthew R. [2 ]
Uscinska, Barbara [2 ]
Hook, Jane M. [2 ]
van Glabbeke, Martine [3 ]
Bramwell, Vivien [4 ]
Lewis, Ian J. [5 ]
Taminiau, Antonie H. M. [6 ]
Nooij, Marianne A. [7 ]
Hogendoorn, Pancras C. W. [8 ]
Gelderblom, Hans [7 ]
Whelan, Jeremy S. [1 ]
机构
[1] Univ Coll Hosp, Dept Oncol, London NW1 2PG, England
[2] Med Res Council Clin Trials Unit, Canc Grp, London, England
[3] European Org Res Treatment Canc Data Ctr, Soft Tissue & Bone Sarcoma Grp, Brussels, Belgium
[4] Tom Baker Canc Clin, Dept Med Oncol, Calgary, AB, Canada
[5] Alder Hey Childrens NHS Fdn Trust, Liverpool, Merseyside, England
[6] Leiden Univ, Med Ctr, Dept Orthopaed Surg, Leiden, Netherlands
[7] Leiden Univ, Med Ctr, Dept Clin Oncol, Leiden, Netherlands
[8] Leiden Univ, Med Ctr, Dept Pathol, Leiden, Netherlands
基金
英国医学研究理事会;
关键词
Osteosarcoma; Toxicity; Survival; Chemotherapy; EARLY LYMPHOCYTE RECOVERY; HIGH-DOSE METHOTREXATE; CELL LUNG-CANCER; HISTOLOGIC RESPONSE; INDUCED NEUTROPENIA; PROGNOSTIC-FACTORS; LYMPHOBLASTIC-LEUKEMIA; OPERABLE OSTEOSARCOMA; YOUNG-ADULTS; EFFICACY;
D O I
10.1016/j.ejca.2011.09.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
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. Crown Copyright (C) 2011 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:703 / 712
页数:10
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