Shely Ryan N, Ratliff Patrick D
Department of Pharmacy Services, Saint Joseph Hospital, Lexington, Kentucky.
Pharmacotherapy. 2014 May;34(5):e34-7. doi: 10.1002/phar.1397. Epub 2014 Jan 4.
Multiple myeloma is the second most common type of hematologic malignancy. It is a B-cell malignancy that affects the bone marrow and often results in thrombocytopenia as well as renal dysfunction. Treatment options range from oral and intravenous chemotherapy to bone marrow transplantation and supportive care. Carfilzomib was approved by the U.S. Food and Drug Administration in 2012 as a treatment option for patients with refractory multiple myeloma who have received at least two previous therapies and have demonstrated recent disease progression. According to the product labeling, the frequency of tumor lysis syndrome (TLS) is less than 1% in patients treated with carfilzomib. To our knowledge, no postmarketing events of TLS have been reported or published. We describe a 55-year-old man with relapsed multiple myeloma who developed a case of TLS that occurred after he received his first two doses of carfilzomib therapy on days 1 and 2; he also had chronic kidney disease secondary to his neoplastic disease. Beginning on day 4, his uric acid levels spiked to critical levels, prompting the use of rasburicase, which returned the levels to within normal limits. His phosphorus and creatinine levels increased during days 5 and 6. On day 8, the patient died, likely due to a combination of disease progression and the adverse effects of treatment. Use of the Naranjo adverse drug reaction probability scale indicated a probable relationship (score of 6) between the patient's development of TLS and carfilzomib therapy. The Hill criteria were used as a secondary measure to ensure causality, which also suggested a link between the patient's development of TLS and the administration of carfilzomib. This case report shows that even the most unlikely of adverse events may occur with medications, especially in the case of a new or recently approved medication. Caution must be taken when deciding to treat and when choosing hydration and premedications with regard to biologic and chemotherapeutic medications. In this case, additional hydration may have been considered. Although given the extent of the adverse reaction combined with the patient's underlying renal dysfunction, extra fluid may or may not have proven beneficial. The use of prophylactic rasburicase or allopurinol could have been considered, but these measures are not typically used with multiple myeloma due to the low incidence of TLS. All things considered, this unlikely adverse reaction may occur in certain patients. If other cases such as this occur, it may be advisable to use TLS prophylaxis in the future in certain patient populations, including those with renal dysfunction or worsening disease states.
多发性骨髓瘤是第二常见的血液系统恶性肿瘤。它是一种B细胞恶性肿瘤,会影响骨髓,常导致血小板减少以及肾功能障碍。治疗选择包括口服和静脉化疗、骨髓移植及支持治疗。卡非佐米于2012年获美国食品药品监督管理局批准,作为难治性多发性骨髓瘤患者的一种治疗选择,这些患者此前至少接受过两种治疗且近期病情有进展。根据药品标签,接受卡非佐米治疗的患者中肿瘤溶解综合征(TLS)的发生率低于1%。据我们所知,尚未有关于TLS的上市后事件报告或发表。我们描述了一名55岁复发型多发性骨髓瘤男性患者,他在第1天和第2天接受头两剂卡非佐米治疗后发生了TLS;他还患有继发于肿瘤疾病的慢性肾脏病。从第4天开始,他的尿酸水平飙升至临界水平,促使使用拉布立酶,使尿酸水平恢复到正常范围。他的磷和肌酐水平在第5天和第6天升高。第8天,患者死亡,可能是疾病进展和治疗不良反应共同作用的结果。使用纳伦霍药物不良反应概率量表显示,患者发生TLS与卡非佐米治疗之间可能存在关联(评分6分)。采用希尔标准作为辅助措施以确定因果关系,这也提示患者发生TLS与使用卡非佐米之间存在联系。本病例报告表明,即使是最不可能发生的不良事件也可能与药物有关,尤其是对于新的或近期获批的药物。在决定治疗方案以及选择生物制剂和化疗药物的水化及预处理措施时必须谨慎。在本病例中,可能应考虑增加水化。尽管鉴于不良反应的程度以及患者潜在的肾功能障碍,额外补液可能证明有益也可能无益。可以考虑使用预防性拉布立酶或别嘌醇,但由于TLS发生率低,这些措施在多发性骨髓瘤患者中通常不使用。综合考虑,这种不太可能发生的不良反应可能在某些患者中出现。如果再发生此类病例,未来在某些患者群体中,包括肾功能不全或病情恶化的患者,可能建议采取TLS预防措施。