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在资源有限的中心,水化持续时间对儿童急性淋巴细胞白血病大剂量甲氨蝶呤诱导的肾毒性的影响:一项随机交叉研究。

Impact of pre-hydration duration on high-dose methotrexate induced nephrotoxicity in childhood acute lymphoblastic leukaemia in resource constraint centers: a randomized crossover study.

机构信息

Department of Pediatrics, Army Hospital Research and Referral, Delhi, 110010, India.

CMO, CH-CRPF, Nagpur, India.

出版信息

Cancer Chemother Pharmacol. 2023 Apr;91(4):331-336. doi: 10.1007/s00280-023-04525-8. Epub 2023 Mar 23.

Abstract

PURPOSE

Hydration before starting high-dose methotrexate (HD-MTX) ensures good renal perfusion and alkaline urinary pH. The duration of pre-hydration is not uniform across protocols. We compared 6-h versus 12-h of pre-hydration for HD-MTX therapy in childhood acute lymphoblastic leukaemia (ALL) at our centre where serial MTX level monitoring is not feasible.

METHODS

This randomised cross-over study consecutively enrolled children  < 12 years with ALL receiving HD-MTX. Children with pre-existing renal disease or those exposed to nephrotoxic drugs were excluded. Two groups receiving 6-h versus 12-h pre-hydration on alternate basis in same patient (each exposed to four cycles of 2-5 g/m of HD-MTX) were compared for HD-MTX induced nephrotoxicity (primary outcome) and other HD-MTX toxicities (HMT) as per common terminology criteria for adverse events (CTCAE-4.0). HD-MTX was administered over 24 h as per BFM-protocol-2009. Solitary MTX levels at 36-h (MTX36) were outsourced and leucovorin (LV) was started at 36 h at 15 mg/m/dose for 6-8 doses 6-hourly depending on MTX36. Hydration fluid was dextrose normal saline with sodium-bicarbonate and administered till last LV dose.

RESULTS

Total 136 HD-MTX cycles in 34 patients (age range 5-144 months) were evaluated. Nephrotoxicity [2/68 (2.9%) in 6-h versus 1/68 (1.5%) in 12-h] and HMT incidence was comparable in two pre-hydration groups. Median MTX36 levels were not affected by duration of hydration irrespective of administered dose of HD-MTX. Median serum creatinine at baseline, post-pre-hydration and at 36-h post start of HD-MTX were comparable.

CONCLUSION

Reduction of pre-hydration duration does not affect HD-MTX induced nephrotoxicity and MTX36 levels in children < 12 years.

摘要

目的

在开始大剂量甲氨蝶呤(HD-MTX)治疗前进行水化可确保良好的肾脏灌注和碱性尿液 pH 值。然而,不同方案中预水化的持续时间并不统一。我们比较了在本中心进行的儿童急性淋巴细胞白血病(ALL)HD-MTX 治疗中 6 小时与 12 小时预水化的效果,本中心无法进行 MTX 水平的连续监测。

方法

这是一项随机交叉研究,连续纳入接受 HD-MTX 治疗的 < 12 岁 ALL 儿童。患有先前存在的肾脏疾病或暴露于肾毒性药物的儿童被排除在外。两组患者在同一患者中交替接受 6 小时与 12 小时预水化(每位患者均接受 4 个 2-5 g/m 的 HD-MTX 周期),根据不良事件通用术语标准(CTCAE-4.0)比较 HD-MTX 诱导的肾毒性(主要结局)和其他 HD-MTX 毒性(HMT)。HD-MTX 按照 BFM-protocol-2009 方案在 24 小时内输注。36 小时时的单剂量 MTX 水平(MTX36)由外部机构检测,LV 在 36 小时时开始,剂量为 15 mg/m/剂量,每 6 小时一次,持续 6-8 次,具体取决于 MTX36。水化液为含有碳酸氢钠的葡萄糖生理盐水,直至最后一次 LV 剂量。

结果

在 34 名患者(年龄 5-144 个月)中评估了总共 136 个 HD-MTX 周期。6 小时预水化组和 12 小时预水化组的肾毒性[2/68(2.9%)与 1/68(1.5%)]和 HMT 发生率相当。无论 HD-MTX 的给药剂量如何,水化时间对 MTX36 水平均无影响。基线、预水化后和 HD-MTX 开始后 36 小时的血清肌酐中位数相似。

结论

在 < 12 岁的儿童中,缩短预水化时间不会影响 HD-MTX 诱导的肾毒性和 MTX36 水平。

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