Jenkins Peter, Wallis Richard
Gloucestershire Oncology Centre, Cheltenham General Hospital, Cheltenham, GL53 7AN, UK.
J Oncol Pharm Pract. 2010 Dec;16(4):251-5. doi: 10.1177/1078155209351304. Epub 2009 Dec 4.
dose-rounding of chemotherapy is increasingly being used in oncology departments to improve the efficiency of outpatient clinics. There is, however, no published data on the effect of this strategy on drug toxicity.
we have analysed acute chemotherapy side effects in a cohort of 662 consecutive patients receiving adjuvant FEC (5-fluorouracil, epirubicin, cyclophosphamide) for breast cancer. A dose-rounding algorithm was used to deliver drug doses that were within 5% of the standard dose based on body surface area.
patients receiving a rounded dose of chemotherapy that was higher than that calculated from their body surface area were not at increased risk of acute haematological or non-haematological toxicity.
dose-rounding of adjuvant FEC within the range ± 5% is not associated with any difference in acute chemotherapy side effects. Longer term follow-up is required to determine whether patients receiving rounded doses below that calculated from their body surface area are at increased risk of relapse.
肿瘤科室越来越多地采用化疗剂量舍入法来提高门诊效率。然而,关于该策略对药物毒性影响的公开数据尚无报道。
我们分析了连续662例接受辅助性FEC(5-氟尿嘧啶、表柔比星、环磷酰胺)治疗乳腺癌患者的急性化疗副作用。采用剂量舍入算法给予基于体表面积在标准剂量±5%范围内的药物剂量。
接受高于根据其体表面积计算所得舍入剂量化疗的患者,急性血液学或非血液学毒性风险并未增加。
辅助性FEC在±5%范围内的剂量舍入与急性化疗副作用方面的差异无关。需要进行长期随访以确定接受低于根据其体表面积计算所得舍入剂量的患者复发风险是否增加。