Servicio de Oncología y Hematología Pediátricas, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Sección de Hematología y Hemoterapia, Hospital Universitario Infanta Sofía, Madrid, Spain.
J Oncol Pharm Pract. 2023 Jun;29(4):794-801. doi: 10.1177/10781552221079568. Epub 2022 Feb 11.
High-dose methotrexate (HDMTX) is administered for the treatment of some cancers. HDMTX is usually safe but may crystallize in renal tubules causing acute kidney injury (AKI). Consequently, MTX elimination is delayed, resulting in a severe and life-threatening condition. No studies have been published about the impact of MTX toxicity in Spain. This study aims to estimate the incidence and management of MTX delayed elimination and toxicity.
A two-round Delphi study was performed to reach consensus between 10 medical experts on haemato-oncology and paediatric oncology with experience in the management of HDMTX treated patients from leading Spanish hospitals. An online questionnaire was developed based on national and international guidelines and previous evidence regarding HDMTX-related toxicity. Consensus was established at 80% agreement. Median and interquartile ranges were calculated, and incidence data were extrapolated to the Spanish general population.
Out of 1.475 patients estimated to receive HDMTX treatment annually in Spain, 27.5% present MTX delayed elimination and 11.6% develop HDMTX-induced AKI (35.4% with severe systemic toxicities (>grade 3) and 18.8% develop chronic renal disease). Mortality is estimated in 4.2%. Immuno-enzymatic assay is used in most of the hospitals (90%) for MTX serum level monitoring. All experts use increased supportive care and high leucovorin as first-line treatment. Available treatments in experts' hospitals in case toxicity persists are haemodialysis (90% of hospitals), glucarpidase (60%) and hemofiltration (50%). Most prevalent non-renal systemic toxicities are haematologic and mucositis (21-40% of patients). Patients with HDMTX-induced AKI require from intensive care (5% of patients), more than 3 sessions and 4 days of dialysis, and about 8.5 days of hospitalization (non-ICU patients) and 12 days in case of patients requiring ICU.
These results are the first evidence regarding HDMTX-induced AKI in Spain. Incidence and mortality results are in line with previous studies. Clinical management is based on preventive measures and the treatment depend on the availability in the hospital. The need for effective, safe and rapid treatment for the reduction of MTX toxic levels and the improvement of monitoring methods were noted by experts as urgent needs. Further observational studies to validate these results would be needed.
高剂量甲氨蝶呤(HDMTX)用于治疗某些癌症。HDMTX 通常是安全的,但可能会在肾小管中结晶,导致急性肾损伤(AKI)。因此,MTX 的消除会延迟,导致严重且危及生命的情况。目前尚未有关于西班牙 MTX 毒性影响的研究。本研究旨在估计 MTX 延迟消除和毒性的发生率和管理。
我们对 10 名来自西班牙领先医院的血液肿瘤学和儿科肿瘤学专家进行了两轮德尔菲研究,以就经验丰富的 HDMTX 治疗患者的 MTX 毒性达成共识。根据国家和国际指南以及以前关于 HDMTX 相关毒性的证据,制定了一份在线问卷。以 80%的一致性达成共识。计算中位数和四分位距,并将发病率数据外推至西班牙普通人群。
在西班牙,每年估计有 1475 名患者接受 HDMTX 治疗,其中 27.5%的患者出现 MTX 延迟消除,11.6%的患者发生 HDMTX 诱导的 AKI(35.4%的患者出现严重全身性毒性(>3 级),18.8%的患者发生慢性肾脏疾病)。死亡率估计为 4.2%。免疫酶联测定法用于大多数医院(90%)监测 MTX 血清水平。所有专家均采用增加支持性护理和高甲酰四氢叶酸作为一线治疗。在专家所在医院,如果毒性持续存在,可采用的治疗方法包括血液透析(90%的医院)、葡萄糖醛酸酶(60%)和血液滤过(50%)。最常见的非肾脏系统毒性是血液学和黏膜炎(21-40%的患者)。HDMTX 诱导的 AKI 患者需要入住重症监护病房(5%的患者),需要进行 3 次以上、4 天以上的透析,需要住院 8.5 天(非 ICU 患者),如果需要入住 ICU,则需要住院 12 天。
这些结果是西班牙首例关于 HDMTX 诱导 AKI 的证据。发病率和死亡率结果与之前的研究一致。临床管理基于预防措施,治疗取决于医院的可用性。专家指出,需要有效的、安全的、快速的治疗方法来降低 MTX 的毒性水平,并改进监测方法。需要进一步的观察性研究来验证这些结果。