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39.0°C 与 38.5°C 耳温作为中性粒细胞减少症癌症化疗患儿发热界限:一项多中心、整群随机、多次交叉、非劣效性试验。

39·0°C versus 38·5°C ear temperature as fever limit in children with neutropenia undergoing chemotherapy for cancer: a multicentre, cluster-randomised, multiple-crossover, non-inferiority trial.

机构信息

Pediatric Hematology and Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Pediatric Oncology, University Children's Hospital of Zürich, University of Zürich, Zürich, Switzerland.

出版信息

Lancet Child Adolesc Health. 2020 Jul;4(7):495-502. doi: 10.1016/S2352-4642(20)30092-4. Epub 2020 Jun 1.

Abstract

BACKGROUND

Fever in neutropenia is the most frequent complication of chemotherapy for cancer. The temperature limit defining fever used clinically varies. A higher limit can avoid unnecessary diagnoses in patients spontaneously recovering from fever. This trial primarily aimed to determine if a limit of 39·0°C ear temperature is non-inferior to 38·5°C regarding safety.

METHODS

This cluster-randomised, multiple crossover, non-blinded, non-inferiority trial was done in six Swiss Paediatric Oncology Group centres (clusters) in Switzerland. Patients (aged 1 to <18 years) with any malignancy and treated with myelosuppressive chemotherapy expected to last 2 months or more were repeatedly randomly assigned (1:1), at the cluster level, to either monthly 39·0°C or 38·5°C ear temperature limits for diagnosis of fever in neutropenia. Diagnosis below the randomised limit was allowed for clinical reasons. Such a diagnosis implied emergency hospitalisation, examinations (including blood culture), as-needed antipyretics, and empirical intravenous broad-spectrum antibiotics. The primary outcome was the rate of fever in neutropenia with safety relevant events (SRE) per chemotherapy year; we also assessed efficacy in terms of rate of fever in neutropenia. The non-inferiority margin was 1·33 for safety, and for effiacy, the superiority margin was 1·00. This trial is registered at ClinicalTrials.gov, number NCT02324231.

FINDINGS

269 patients were recruited between April 28, 2016, to Aug 27, 2018, until the trial was stopped for success after the second interim analysis. Patients were repeatedly randomly assigned, with 1210 (48%) of 2547 randomisation periods and 92 (47%) of 195 chemotherapy years randomised to 39·0°C. SREs were diagnosed in 72 (20%) of 360 fever in neutropenia episodes (zero deaths, 16 intensive care unit admissions, 22 cases of severe sepsis, and 56 cases of bacteraemia). In 92 chemotherapy years randomised to the 39·0°C fever limit, 151 episodes of fever with neutropenia were diagnosed (1·64 per year), including 22 (15%) with SRE (0·24 per year). In 103 chemotherapy years randomised to 38·5°C, 209 episodes were diagnosed (2·03 per year), including 50 (24%) with SRE (0·49 per year). The mixed Poisson regression rate ratio (RR) of fever in neutropenia with SRE in 39·0°C versus 38·5°C was 0·56 (95% upper confidence bound 0·72). The corresponding RR of fever in neutropenia was 0·83 (95% upper confidence bound 0·98).

INTERPRETATION

In children with neutropenia and chemotherapy for cancer, 39·0°C ear temperature was safe and seemed efficacious. For Switzerland and comparable settings, 39·0°C can be recommended as new evidence-based standard fever limit except for patients with acute myeloid leukaemia or haematopoietic stem cell transplantation.

FUNDING

Swiss Cancer League (KLS-3645-02-2015).

摘要

背景

中性粒细胞减少症并发发热是癌症化疗最常见的并发症。临床上用于定义发热的温度界限有所不同。较高的温度界限可以避免在患者从发热中自然恢复时进行不必要的诊断。本试验主要旨在确定耳温 39.0°C 的界限是否在安全性方面不劣于 38.5°C。

方法

这是一项在瑞士六家瑞士儿科肿瘤学组中心(集群)进行的集群随机、多次交叉、非盲、非劣效性试验。预计持续 2 个月或更长时间接受骨髓抑制性化疗的任何恶性肿瘤患者(年龄 1 至<18 岁),反复随机(1:1)按集群水平分配至每月 39.0°C 或 38.5°C 的耳温界限,以诊断中性粒细胞减少症发热。出于临床原因允许在随机界限以下进行诊断。这样的诊断意味着紧急住院、检查(包括血培养)、按需退热、经验性静脉内广谱抗生素。主要结局是每化疗年中性粒细胞减少症发热相关不良事件(SRE)的发生率;我们还评估了发热性中性粒细胞减少症的疗效。安全性的非劣效性边界为 1.33,疗效的优越性边界为 1.00。该试验在 ClinicalTrials.gov 上注册,编号为 NCT02324231。

结果

2016 年 4 月 28 日至 2018 年 8 月 27 日期间共招募了 269 名患者,在第二次中期分析后因成功而停止试验。患者反复随机分配,在 2547 次随机分配期的 1210 次(48%)和 92 次(47%)化疗年中,1210 次(48%)和 92 次(47%)随机分配到 39.0°C。在 360 次中性粒细胞减少性发热发作中诊断出 72 次(20%)发热相关不良事件(无死亡、16 例 ICU 入院、22 例严重脓毒症和 56 例菌血症)。在随机到 39.0°C 发热界限的 92 个化疗年中,诊断出 151 次发热伴中性粒细胞减少症(每年 1.64 次),其中 22 次(15%)伴有 SRE(每年 0.24 次)。在随机到 38.5°C 的 103 个化疗年中,诊断出 209 次发热伴中性粒细胞减少症(每年 2.03 次),其中 50 次(24%)伴有 SRE(每年 0.49 次)。39.0°C 与 38.5°C 相比,发热伴 SRE 的混合泊松回归率比(RR)为 0.56(95%置信上限为 0.72)。发热伴中性粒细胞减少症的相应 RR 为 0.83(95%置信上限为 0.98)。

解释

在患有中性粒细胞减少症和癌症化疗的儿童中,39.0°C 的耳温是安全的,似乎有效。对于瑞士和类似的环境,除了患有急性髓系白血病或造血干细胞移植的患者外,39.0°C 可被推荐为新的基于证据的发热界限。

资金

瑞士癌症协会(KLS-3645-02-2015)。

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