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食管癌同步放化疗:影响骨髓毒性的因素

Concurrent chemoradiation for oesophageal cancer: factors influencing myelotoxicity.

作者信息

MacKean J, Burmeister B H, Lamb D S, Denham J W

机构信息

Radiation Oncology Department, Newcastle Mater Misericordiae Hospital, New South Wales, Australia.

出版信息

Australas Radiol. 1996 Nov;40(4):424-9. doi: 10.1111/j.1440-1673.1996.tb00440.x.

Abstract

Concurrent chemotherapy and radiation (CT/RT) for localized oesophageal cancer can cause life-threatening myelosuppression. This non-randomized study examines 95 patients from three Australasian centres treated on the Trans-Tasman Radiation Oncology "definitive' chemoradiation study. Duration of fluorouracil infusion and patient age were independently predictive of myelotoxicity after the first cycle of CT/RT. Overall rates of grade III and IV neutropaenia were 23% and of thrombocytopaenia 8% following the first cycle of chemotherapy. Five neutropaenic septic episodes followed the first cycle and six the second. All five patients recovered after the first cycle but there were four treatment-related deaths occurring after the second cycle of CT/RT. Recommendations are made concerning initial dosing, dose reductions and delays to minimize adverse patient outcomes from myelosuppression.

摘要

同步放化疗(CT/RT)治疗局部食管癌可导致危及生命的骨髓抑制。这项非随机研究对来自三个澳大拉西亚中心的95例患者进行了观察,这些患者参与了跨塔斯曼放射肿瘤学“确定性”放化疗研究。氟尿嘧啶输注时间和患者年龄是CT/RT第一个周期后骨髓毒性的独立预测因素。化疗第一个周期后,III级和IV级中性粒细胞减少的总体发生率分别为23%,血小板减少的发生率为8%。第一个周期后发生了5次中性粒细胞减少性败血症,第二个周期有6次。所有5例患者在第一个周期后康复,但在CT/RT第二个周期后有4例与治疗相关的死亡。文中就初始剂量、剂量减少和延迟给药提出了建议,以尽量减少骨髓抑制对患者产生的不良后果。

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