Ridolfi L, Barisone E, Vivalda M, Vivenza C, Brach Del Prever A, Leone L, Miniero R
Dipartimento di Scienze Pediatriche e dell'Adolescenza, Universitá degli Studi, Torino.
Minerva Pediatr. 1996 May;48(5):193-200.
We evaluated and compared hematologic, hepatic and renal cumulative toxicity of high dose methotrexate (HDMTX) repeated courses in two groups of pediatric patients: 22 patients affected by "non B" acute lymphoblastic leukemia (ALL) treated, in consolidation phase, with four courses of HDMTX 5 g/mq given intravenously over 24 hours infusion (for a total of 88 courses) according to the Italian Cooperative Protocols AIEOP LLA-88; 18 patients affected by non metastatic osteosarcoma of extremities (OST) treated, in preoperative and postoperative phases, with five courses of HDMTX 8 g/mq given intravenously over 6 hours infusion (for a total of 90 courses) according to CNR-NEO 2 protocol. Severe myelosuppression (neutropenia < 500/microliters and/or thrombocytopenia < 25000/microliters) was more frequently observed in ALL (7% of infusions) than in OST (3%). Hepatotoxicity (serum transaminase elevation > 350 IU/l) was significantly more frequent (p < 0.001) in OST (32% of courses) than ALL (6%). Nephrotoxicity was assimilable in the two groups and the elevation of serum creatinine was never higher than 1.9 mg/dl. We did not observe any increase of hematologic, hepatic and renal toxicity following the HDMTX courses repetition.
我们评估并比较了两组儿科患者高剂量甲氨蝶呤(HDMTX)重复疗程的血液学、肝脏和肾脏累积毒性:22例“非B”急性淋巴细胞白血病(ALL)患者,在巩固期,根据意大利合作方案AIEOP LLA - 88,接受4个疗程的HDMTX,剂量为5 g/m²,静脉输注24小时(共88个疗程);18例四肢非转移性骨肉瘤(OST)患者,在术前和术后阶段,根据CNR - NEO 2方案,接受5个疗程的HDMTX,剂量为8 g/m²,静脉输注6小时(共90个疗程)。严重骨髓抑制(中性粒细胞减少<500/微升和/或血小板减少<25000/微升)在ALL患者中(7%的输注)比在OST患者中(3%)更常见。肝毒性(血清转氨酶升高>350 IU/l)在OST患者中(32%的疗程)比ALL患者(6%)显著更常见(p<0.001)。两组的肾毒性相似,血清肌酐升高从未超过1.9 mg/dl。我们未观察到HDMTX疗程重复后血液学、肝脏和肾脏毒性有任何增加。