Tolerability Assessment of Tyrosine Kinase Inhibitors in Patients With Solid Tumor Malignancies and Hypoalbuminemia.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Sarvnaz Sadrameli, Sydney Bringgold, Elizabeth Dow-Hillgartner
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Abstract

Background: Hypoalbuminemia is common in patients with advanced solid tumor malignancies. However, despite the increased use of highly protein-bound tyrosine kinase inhibitors (TKIs) in cancer treatments, the tolerability of these agents in patients with hypoalbuminemia is not fully known.

Objective: Our aim is to assess whether patients on oral TKIs with hypoalbuminemia are at higher risk for experiencing medication-related adverse events, therefore requiring careful considerations.

Methods: This is a single-center, retrospective study including patients ≥18 years of age with a solid tumor malignancy who had taken at least one dose of oral TKIs with a protein binding of ≥90% between June 1, 2016, and June 1, 2021. The primary outcome was to compare time to TKI discontinuation due to adverse events between patients with and without hypoalbuminemia. Key secondary outcomes include TKI discontinuation and dose reduction rates, time to TKI dose reduction, and severity of adverse events.

Results: Out of 282 included patients, 134 (48%) patients had hypoalbuminemia and 148 (52%) had normal albumin levels. Compared with patients without hypoalbuminemia, patients with hypoalbuminemia had shorter median time on treatment at 2.8 months (95% CI = 2.3-4.5 months) versus 4.3 months (95% CI = 2.8-6.4 months; P = 0.003). In patients who had TKI discontinuation, dose reduction was associated with longer time on treatment in patients in the normal albumin group compared with patients in the hypoalbuminemia group or patients without dose reduction (P < 0.0001). Patients in the hypoalbuminemia group experienced significantly more grade 3/4 adverse events compared with those in the normal albumin group (73% vs 27%, P < 0.0001).

Conclusion and relevance: Hypoalbuminemia is a risk factor for both shorter time on treatment and more severe adverse events in patients with solid tumor malignancies taking highly protein-bound oral TKIs. This study highlights the need for closer monitoring of this patient population by health care providers.

酪氨酸激酶抑制剂在实体瘤恶性肿瘤和低白蛋白血症患者中的耐受性评估
背景:低白蛋白血症常见于晚期实体瘤恶性肿瘤患者。然而,尽管在癌症治疗中越来越多地使用高蛋白结合型酪氨酸激酶抑制剂(TKIs),但这些药物在低白蛋白血症患者中的耐受性尚不完全清楚:我们的目的是评估患有低白蛋白血症的口服 TKIs 患者发生药物相关不良事件的风险是否更高,因此需要慎重考虑:这是一项单中心回顾性研究,研究对象包括在 2016 年 6 月 1 日至 2021 年 6 月 1 日期间至少服用过一次蛋白结合率≥90% 的口服 TKIs、年龄≥18 岁的实体瘤恶性肿瘤患者。主要结果是比较有和没有低白蛋白血症的患者因不良事件而停用TKI的时间。主要次要结果包括TKI停药率和减量率、TKI减量时间以及不良事件的严重程度:在纳入的 282 例患者中,134 例(48%)患者有低白蛋白血症,148 例(52%)患者白蛋白水平正常。与没有低白蛋白血症的患者相比,低白蛋白血症患者的中位治疗时间更短,为 2.8 个月(95% CI = 2.3-4.5 个月)对 4.3 个月(95% CI = 2.8-6.4 个月;P = 0.003)。在停用TKI的患者中,与低白蛋白血症组或未减少剂量的患者相比,白蛋白正常组患者减少剂量与延长治疗时间有关(P < 0.0001)。与白蛋白正常组相比,低白蛋白血症组患者发生 3/4 级不良事件的比例明显更高(73% vs 27%,P < 0.0001):对于服用高蛋白结合型口服 TKIs 的实体瘤恶性肿瘤患者来说,低白蛋白血症是缩短治疗时间和增加严重不良事件的风险因素。这项研究强调了医疗服务提供者对这一患者群体进行更密切监测的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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