Department of Pharmacy, Nagoya City University Hospital, 1-Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya, Aichi, 467-8602, Japan.
Department of Hospital Pharmacy, Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1, Tanabe dori, Mizuho ku, Aichi, 467-8603, Nagoya, Japan.
BMC Cancer. 2020 Nov 17;20(1):1117. doi: 10.1186/s12885-020-07592-9.
Novel agents such as proteasome inhibitors have been developed for several years to treat multiple myeloma. Although multiple myeloma is a low-risk disease for developing tumor lysis syndrome (TLS), treatment with these novel therapies might increase TLS risk. Previous studies, mostly case reports or case series, have reported bortezomib-induced TLS in patients with multiple myeloma. This study aimed to investigate risk factors associated with TLS development in multiple myeloma patients.
We retrospectively investigated incidences of laboratory and clinical TLS (LTLS and CTLS, respectively) in patients who received primary therapy for treatment-naive, symptomatic multiple myeloma between May 2007 and January 2018. We used multivariate logistic regression analyses to evaluate the associations between TLS and several parameters previously reported to be associated with increased risk.
This study included 210 patients with multiple myeloma, of which ten (4.8%) had LTLS and seven (3.3%) had CTLS. The characteristics of the administered anticancer or prophylactic antihyperuricemic agents were similar between patients with and without TLS. Multivariate analyses revealed that TLS was most strongly associated with bortezomib-containing therapy (odds ratio = 3.40, P = 0.069), followed by male sex (odds ratio = 2.29, P = 0.153). In a subgroup analysis focused on men, treatment with bortezomib-containing therapy was significantly associated with increased risk of TLS (odds ratio = 8.51, P = 0.046).
In the present study, we investigated the risk factors associated with TLS development in 210 multiple myeloma patients, which, to the best of our knowledge, is the largest number of patients reported to date. Furthermore, this study is the first to evaluate TLS risk factors in MM by adjusting for the effects of potential confounding factors in patients' backgrounds. Consequently, we found that bortezomib-containing therapy increases the risk of TLS in male patients with multiple myeloma. TLS risk should be evaluated further in low-risk diseases such as multiple myeloma, since a significant number of novel therapies can achieve high antitumor responses.
新型药物如蛋白酶体抑制剂已被开发用于治疗多发性骨髓瘤多年。尽管多发性骨髓瘤发生肿瘤溶解综合征(TLS)的风险较低,但这些新型疗法的治疗可能会增加 TLS 的风险。之前的研究主要是病例报告或病例系列,报道了硼替佐米诱导的多发性骨髓瘤患者发生 TLS。本研究旨在探讨多发性骨髓瘤患者发生 TLS 的相关危险因素。
我们回顾性地调查了 2007 年 5 月至 2018 年 1 月期间接受初治、有症状的多发性骨髓瘤患者的原发性治疗的患者中实验室和临床 TLS(LTLS 和 CTLS)的发生率。我们使用多变量逻辑回归分析来评估 TLS 与之前报道的与风险增加相关的几个参数之间的关系。
本研究包括 210 例多发性骨髓瘤患者,其中 10 例(4.8%)发生 LTLS,7 例(3.3%)发生 CTLS。接受抗癌或预防性降尿酸药物的患者的特征在有 TLS 和无 TLS 的患者之间相似。多变量分析显示,TLS 与硼替佐米治疗密切相关(比值比=3.40,P=0.069),其次是男性(比值比=2.29,P=0.153)。在专注于男性的亚组分析中,硼替佐米治疗与 TLS 风险增加显著相关(比值比=8.51,P=0.046)。
在本研究中,我们调查了 210 例多发性骨髓瘤患者发生 TLS 的相关危险因素,据我们所知,这是迄今为止报告的最大患者人数。此外,这项研究首次通过调整患者背景中潜在混杂因素的影响来评估 MM 中的 TLS 危险因素。因此,我们发现硼替佐米治疗会增加男性多发性骨髓瘤患者发生 TLS 的风险。在多发性骨髓瘤等低风险疾病中,应进一步评估 TLS 风险,因为许多新型疗法可以实现高抗肿瘤反应。