Bakhsh Sabirin, Khan Mansoor Ahmed, Alshamrani Majed, Mufti Roula, Naeem Anjum, AlMansour Mubarak, Alsaeed Ahmad, Alahmari Mousa, Aseeri Mohammed
Pharmaceutical Care Services, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Jeddah, SAU.
Medical Affairs, Johnson & Johnson Innovative Medicine, Riyadh, SAU.
Cureus. 2024 Sep 4;16(9):e68664. doi: 10.7759/cureus.68664. eCollection 2024 Sep.
Tumor lysis syndrome (TLS) is a critical and potentially fatal complication linked to specific types of cancer. Rasburicase stands as a crucial medication necessary for the prevention and treatment of hyperuricemia, a condition commonly associated with TLS. Due to a shortage of rasburicase during the COVID-19 pandemic, a fixed-dose strategy of 3 mg rasburicase was used in many adult cancer patients in our center.
The objective of this study was to assess the effectiveness of a fixed dose of 3 mg rasburicase in preventing and managing hyperuricemia associated with TLS in adult cancer patients.
We conducted a retrospective, observational cohort study between March 2020 and February 2022. The study included adult patients who received a fixed dose of 3 mg rasburicase. The primary outcome measure was the reduction in serum uric acid (UA) levels at 24 and 48 hours after treatment, with the aim of achieving and maintaining normal UA levels.
Seventeen patients in the treatment group and 20 patients in the prevention group were included. In the treatment group, 15 (88%) patients had normalization of serum UA, which is considered to be <7 mg/dL (median: 4.48 mg/dL) at 24 hours, and 16 (94%) patients had achieved normal UA at 48 hours (median: 2.78 mg/dL) after receiving the rasburicase dose. In the prevention group, all 20 (100%) patients achieved normal UA at 24 hours after receiving the rasburicase dose.
Based on these findings, a single fixed dose of 3 mg rasburicase is effective for preventing and managing hyperuricemia associated with TLS in high-risk patients.
肿瘤溶解综合征(TLS)是一种与特定类型癌症相关的严重且可能致命的并发症。拉布立酶是预防和治疗高尿酸血症(一种通常与TLS相关的病症)所需的关键药物。在新冠疫情期间,由于拉布立酶短缺,我们中心的许多成年癌症患者采用了3毫克拉布立酶的固定剂量策略。
本研究的目的是评估3毫克固定剂量的拉布立酶在预防和管理成年癌症患者中与TLS相关的高尿酸血症方面的有效性。
我们在2020年3月至2022年2月期间进行了一项回顾性观察队列研究。该研究纳入了接受3毫克固定剂量拉布立酶的成年患者。主要结局指标是治疗后24小时和48小时血清尿酸(UA)水平的降低,目标是达到并维持正常的UA水平。
治疗组纳入17例患者,预防组纳入20例患者。在治疗组中,15例(88%)患者在24小时时血清UA正常化,即<7毫克/分升(中位数:4.48毫克/分升),16例(94%)患者在接受拉布立酶剂量后48小时达到正常UA(中位数:2.78毫克/分升)。在预防组中,所有20例(100%)患者在接受拉布立酶剂量后24小时达到正常UA。
基于这些发现,单一固定剂量的3毫克拉布立酶对预防和管理高危患者中与TLS相关的高尿酸血症有效。