Jim Heather S L, Eisel Sarah L, Hoogland Aasha I, Shaw Sandra, King Jennifer C, Dicker Adam P
Moffitt Cancer Center, Department of Health Outcomes and Behavior, Tampa, FL 33612, USA.
GO2 Foundation for Lung Cancer, Washington, DC 20006, USA.
Cancers (Basel). 2020 Dec 31;13(1):103. doi: 10.3390/cancers13010103.
Immune checkpoint inhibitors (ICIs) are increasingly used for advanced lung cancer, but few studies have reported on patient-reported outcomes (PROs) outside the context of a clinical trial. The goal of the current study was to assess PROs in participants of a lung cancer registry who had been treated with an ICI. Patients participating in the GO Foundation's Lung Cancer Registry who reported receiving atezolizumab, durvalumab, nivolumab, or pembrolizumab were invited to participate in a survey about their experiences during treatment. Quality of life was evaluated using the Functional Assessment of Cancer Therapy-General (FACT-G). Common symptomatic adverse events were evaluated using an item bank generated for ICIs. Internationally, 226 patients (mean age 61, 75% female) participated. Patients reported worse quality of life at the time of assessment than U.S. population and cancer normative samples. The most common moderate to severe adverse events during ICI treatment were fatigue (41%), aching joints (27%), and aching muscles (20%). Due to toxicity, 25% reported a treatment delay, 11% an emergency room visit, and 9% a hospitalization. This study is among the first to our knowledge to report on PROs of ICIs outside the context of a clinical trial. Results suggest higher rates of adverse events than previously reported in clinical trials.
免疫检查点抑制剂(ICI)越来越多地用于治疗晚期肺癌,但很少有研究报道在临床试验背景之外患者报告的结局(PRO)。本研究的目的是评估接受ICI治疗的肺癌登记参与者的PRO。邀请参与GO基金会肺癌登记的报告接受阿替利珠单抗、度伐利尤单抗、纳武利尤单抗或帕博利珠单抗治疗的患者参与一项关于其治疗期间经历的调查。使用癌症治疗功能评估通用量表(FACT-G)评估生活质量。使用为ICI生成的项目库评估常见的症状性不良事件。在国际上,226名患者(平均年龄61岁,75%为女性)参与了研究。患者报告在评估时的生活质量比美国人群和癌症标准样本更差。ICI治疗期间最常见的中度至重度不良事件为疲劳(41%)、关节疼痛(27%)和肌肉疼痛(20%)。由于毒性,25%的患者报告治疗延迟,11%的患者到急诊室就诊,9%的患者住院。据我们所知,本研究是首批报告临床试验背景之外ICI的PRO的研究之一。结果表明不良事件发生率高于先前临床试验报告的发生率。