FITNESS 研究:纵向老年病学评估、治疗毒性和生物样本采集,以评估老年肺癌患者的功能障碍情况

M. Grogan, R. Hoyd, Jason Benedict, Sarah Janse, N. Williams, Michelle Naughton, Christin E. Burd, E. Paskett, Ashley E. Rosko, Daniel J. Spakowicz, Carolyn Presley
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引用次数: 0

摘要

患有慢性疾病的老年人优先考虑功能独立性。我们旨在描述使用纵向老年综合评估(CGA)和老化分子生物标志物捕捉肺癌老年患者功能障碍和治疗毒性的可行性。这项前瞻性研究纳入了年龄≥60 岁、新诊断为非小细胞肺癌的成年人。参与者从俄亥俄州中部招募(2018-2020年)。研究评估包括基线、3、6 和 12 个月时的癌症与衰老研究小组 CGA(CARG-CGA)、短期体能表现电池(SPPB)和祝福定向记忆浓度(BOMC)测试。每月采集日常生活活动(ADL)和工具性日常生活活动(IADL)、生活质量(QoL,PROMIS 10)和治疗毒性。该研究共招募了 50 名参与者,平均年龄为 71.7 岁。92%的参与者为白种人,58%为男性,均为非西班牙裔。大多数患者为晚期(III/IV 期:90%;I/II 期:10%),腺癌是主要的组织学亚型(68% 对 24%,鳞状)。一线治疗包括化疗(44%)、免疫检查点抑制剂(ICIs,22%)、化疗和 ICIs(30%)或酪氨酸激酶抑制剂(4%)。基线 CARG 毒性评分的中位数为 8(范围为 2-12)。在出现治疗相关毒性的患者(n = 49)中,39 例(79.6%)为轻度(1-2 级),10 例(20.4%)为中度至重度(≥ 3 级)。CARG评分≥8分者的治疗毒性更大(28.0%对13.6%)。基线时较高的 IADL 独立性、QoL 和 SPPB 评分与 Candidatus Gastranaerophilales 菌、Lactobacillus rogosae 和 Enterobacteria phage P4 呈正相关。在接受肺癌治疗的老年人中,进行纵向 CGA 和生物标志物收集是可行的。肠道微生物和 T 细胞基因表达变化与主观和客观功能状态评估相关。未来的研究将检验这些关联的因果关系,以便通过新型支持性护理干预来改善预后,预防功能性残疾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The FITNESS study: longitudinal geriatric assessment, treatment toxicity, and biospecimen collection to assess functional disability among older adults with lung cancer
Older adults with chronic disease prioritize functional independence. We aimed to describe the feasibility of capturing functional disability and treatment toxicity among older adults with lung cancer using a longitudinal comprehensive geriatric assessment (CGA) and molecular biomarkers of aging.This prospective study included adults ≥60 years with any newly diagnosed non-small-cell lung cancer. Participants were recruited from central Ohio (2018–2020). Study assessments included the Cancer and Aging Research Group CGA (CARG-CGA), short physical performance battery (SPPB), and the blessed orientation-memory concentration (BOMC) test at baseline, 3, 6, and 12 months. Activities of daily living (ADLs) and instrumental ADLs (IADLs), quality of life (QoL, PROMIS 10), and treatment toxicity were captured monthly. Stool and blood were collected to characterize the gut microbiome and age-related blood biomarkers.This study enrolled 50 participants with an average age of 71.7 years. Ninety-two percent of participants were Caucasian, 58% were male, and all were non-Hispanic. Most had advanced stage (stage III/IV: 90%; stage I/II: 10%), with adenocarcinoma the predominant histologic subtype (68% vs. 24% squamous). First-line treatments included chemotherapy (44%), immune checkpoint inhibitors (ICIs, 22%), chemotherapy and ICIs (30%), or tyrosine kinase inhibitors (4%). The median baseline CARG toxicity score was 8 (range 2–12). Among patients with treatment-related toxicity (n = 49), 39 (79.6%) cases were mild (grade 1–2), and 10 (20.4%) were moderate to severe (≥ grade 3). Treatment toxicity was greater among those with a CARG score ≥8 (28.0% vs. 13.6%). Higher IADL independence, QoL, and SPPB scores at baseline were positively associated with Candidatus Gastranaerophilales bacterium, Lactobacillus rogosae, and Enterobacteria phage P4. Romboutsia ilealis, Streptococcus, and Lachnoclostridium sp An138 and T cell lag3 and cd8a were associated with worse IADLs, QoL, and SPPB scores at baseline.A longitudinal CGA and biomarker collection is feasible among older adults undergoing lung cancer treatment. Gut microbe and T cell gene expression changes correlated with subjective and objective functional status assessments. Future research will test causality in these associations to improve outcomes through novel supportive care interventions to prevent functional disability.
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