Friedman Claire F, Clark Varina, Raikhel Andrew V, Barz Tim, Shoushtari Alexander N, Momtaz Parisa, Callahan Margaret K, Wolchok Jedd D, Chapman Paul B, Hellmann Matthew D, Postow Michael A
Affiliations of authors: Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY (CFF, VC, TB, ANS, PM, MKC, JDW, PBC, MDH, MAP); Weill Cornell Medical College, New York, NY (CFF, AVR, ANS, PM, MKC, JDW, PBC, MDH, MAP).
J Natl Cancer Inst. 2016 Dec 31;109(4). doi: 10.1093/jnci/djw260. Print 2017 Apr.
The Common Terminology Criteria for Adverse Events (CTCAE) were developed to document the adverse effects of chemotherapy but are now also used to document immune-related adverse events (irAE). Characterization of irAE by the CTCAE has implications for determining dose-limiting toxicity (DLT) and, consequently, the recommended phase II dose (RP2D) of investigational agents. In the phase I trial of nivolumab + ipilimumab, an asymptomatic increase in lipase was the primary DLT that informed the RP2D. We performed a retrospective study of 119 patients with melanoma who were treated at Memorial Sloan Kettering Cancer Center with the combination of nivolumab + ipilimumab to investigate the relationship between asymptomatic grade 3 or higher increases in amylase and/or lipase and pancreatitis, a known irAE. Of the 119 patients, there were only two cases of pancreatitis, representing 20% of patients with grade 3 or higher amylase, 6.3% of patients with grade 3 or higher lipase, and 20% of patients with grade 3 or higher elevations of both enzymes. The application of the CTCAE, especially in grading independent lab values, should be considered carefully in clinical trials of novel immunotherapeutic agents.
不良事件通用术语标准(CTCAE)最初是为记录化疗的不良反应而制定的,但现在也用于记录免疫相关不良事件(irAE)。通过CTCAE对irAE进行特征描述,对于确定剂量限制性毒性(DLT)以及由此确定研究药物的推荐II期剂量(RP2D)具有重要意义。在纳武单抗+伊匹单抗的I期试验中,脂肪酶无症状升高是确定RP2D的主要DLT。我们对119例在纪念斯隆凯特琳癌症中心接受纳武单抗+伊匹单抗联合治疗的黑色素瘤患者进行了一项回顾性研究,以调查淀粉酶和/或脂肪酶无症状性3级或更高水平升高与已知irAE胰腺炎之间的关系。在这119例患者中,仅有2例胰腺炎病例,分别占淀粉酶3级或更高水平患者的20%、脂肪酶3级或更高水平患者的6.3%以及两种酶均3级或更高水平升高患者的20%。在新型免疫治疗药物的临床试验中,应谨慎考虑CTCAE的应用,尤其是在对独立实验室值进行分级时。