Musculoskeletal Oncology Center, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510080, China.
Cancer Chemother Pharmacol. 2018 Aug;82(2):221-227. doi: 10.1007/s00280-018-3592-x. Epub 2018 May 28.
This study aimed to explore whether peak serum methotrexate concentration (C) correlated with adverse events, overall survival (OS) and event-free survival (EFS) in patients with primary extremity osteosarcoma.
Patients with extremity osteosarcoma who were treated at our center between 2005 and 2015 were retrospectively studied. All the patients were Enneking stage II and had received standard perioperative chemotherapy composed of high-dose methotrexate, doxorubicin, cisplatin and ifosfamide. C and treatment-associated toxicities of each cycle were recorded. OS and EFS were estimated and compared by Kaplan-Meier survival analysis, and Cox regression models were performed for univariate comparisons.
In total, 567 patients were followed for an average of 53 months (24-104 months). The estimated 3- and 5-year EFS were 71.7 and 63.1%, and the 3- and 5-year OS were 78.2 and 72.9%, respectively. C ranged from 527 to 2495 µmol/L with a mean value of 931 ± 106 µmol/L. No significant differences in EFS and OS (p = 0.18 and p = 0.28) were observed among patients with a mean C > 1500, > 1000, > 700 and < 700 µmol/L. However, patients with a mean C > 1500 µmol/L had significantly increased rates of grade 3-5 toxicity. In the univariate analysis, C was not a prognostic factor for EFS (p = 0.08) or OS (p = 0.16).
C did not correlate significantly with the oncologic prognosis of non-metastatic extremity osteosarcoma patients treated by multi-agent chemotherapy; however, C correlated closely with toxicities and complications. The persistent inclusion of methotrexate in classical multidisciplinary chemotherapy was questioned and should be examined in future trials.
本研究旨在探讨初诊肢体骨肉瘤患者的血清甲氨蝶呤峰浓度(C)与不良事件、总生存(OS)和无事件生存(EFS)是否相关。
回顾性分析 2005 年至 2015 年在我院治疗的肢体骨肉瘤患者。所有患者均为 Enneking Ⅱ期,接受大剂量甲氨蝶呤、多柔比星、顺铂和异环磷酰胺组成的标准围手术期化疗。记录每个周期的 C 和治疗相关毒性。采用 Kaplan-Meier 生存分析比较 OS 和 EFS,采用单因素 Cox 回归模型进行比较。
共 567 例患者平均随访 53 个月(24-104 个月)。估计 3 年和 5 年 EFS 分别为 71.7%和 63.1%,3 年和 5 年 OS 分别为 78.2%和 72.9%。C 范围为 527-2495μmol/L,平均为 931±106μmol/L。C 均值>1500、>1000、>700 和<700μmol/L 的患者 EFS 和 OS 无显著差异(p=0.18 和 p=0.28)。然而,C 均值>1500μmol/L 的患者的 3-5 级毒性发生率显著增加。单因素分析显示,C 不是 EFS(p=0.08)或 OS(p=0.16)的预后因素。
C 与多药化疗治疗非转移性肢体骨肉瘤患者的肿瘤预后无显著相关性;但 C 与毒性和并发症密切相关。经典多学科化疗中持续包含甲氨蝶呤受到质疑,应在未来的试验中进行检验。