Favre R, Monjanel S, Alfonsi M, Pradoura J P, Bagarry-Liegey D, Clement S, Imbert A M, Lena N, Colonna d'Istria J, Cano J P, Carcassonne Y
Cancer Chemother Pharmacol. 1982;9(3):156-60. doi: 10.1007/BF00257744.
Some of 66 patients with head and neck tumors were treated with high-dose methotrexate monochemotherapy. The use of a prospective mathematical model with pharmacokinetic surveillance proved to be reliable, practical, and useful. By this means chemotherapy could be individualized, with a resultant marked reduction in the frequency and severity of toxicity. The onset of clinical toxic manifestations was significantly correlated with a poor therapeutic response and poor prognosis. The patients were classified in to three groups according to poor, intermediate, and good pharmacokinetic parameters calculated after an intravenous identification dose of methotrexate. These group allocations had a very high prognostic value with regard to toxicity, and especially to the quality of therapeutic response to high-dose methotrexate. They are suggested as useful guidelines in the prescription of high-dose methotrexate chemotherapy.
66例头颈部肿瘤患者中部分接受了大剂量甲氨蝶呤单一化疗。采用具有药代动力学监测的前瞻性数学模型被证明是可靠、实用且有用的。通过这种方式,化疗可以个体化,从而使毒性的频率和严重程度显著降低。临床毒副反应的发生与治疗反应不佳和预后不良显著相关。根据静脉注射甲氨蝶呤识别剂量后计算出的药代动力学参数差、中等和良好,将患者分为三组。这些分组在毒性方面,尤其是对大剂量甲氨蝶呤治疗反应的质量方面具有很高的预后价值。它们被建议作为大剂量甲氨蝶呤化疗处方中的有用指导原则。