SABR for Early Non-Small Cell Lung Cancer: Changes in Pulmonary Function, Dyspnea, and Quality of Life

医学 肺癌 生活质量(医疗保健) 肺功能测试 SABR波动模型 队列 DLCO公司 内科学 前瞻性队列研究 队列研究 扩散能力 肺功能 经济 护理部 金融经济学 波动性(金融) 随机波动
作者
Julie Ahn,Roland Yeghiaian‐Alvandi,Fiona Hegi‐Johnson,Lois Browne,Peter Graham,Yaw Chin,Harriet E. Gee,Shalini Vinod,Jane Ludbrook,Andrew Last,Patrick Dwyer,Anselm Ong,Noel J. Aherne,Maria Azzi,Eric Hau
出处
期刊:International Journal of Radiation Oncology Biology Physics [Elsevier BV]
卷期号:117 (5): 1213-1221 被引量:1
标识
DOI:10.1016/j.ijrobp.2023.07.017
摘要

Purpose The aim of this study was to report pulmonary function tests (PFTs) and clinician-reported and patient-reported quality-of-life (QoL) outcomes on a cohort of patients with non-small cell lung cancer (NSCLC) treated with SABR. Methods and Materials A total of 119 patients with NSCLC were treated with SABR in the prospective cohort SSBROC study of patients with T1-T2N0M0 NSCLC. PFTs and QoL measures were obtained at baseline pretreatment and at 6-month intervals. Here we report on the 6- to 18-month time points. Analysis of covariance (ANCOVA) methods adjusting for baseline analyzed potential predictors on outcomes of PFTs and patient-reported dyspnea at 18 months. Results The only statistically significant decline in PFTs was seen in forced expiratory volume in 1 second (FEV1) at 18 months post-SABR, with a decline of −0.11 L (P = .0087; 95% CI, −0.18 to −0.02). Of potential predictors of decline, only a 1-unit increase in smoking pack-years resulted in a −0.12 change in diffusing capacity for carbon monoxide (P = .026; 95% CI, −0.02 to −0.23) and a 0.003 decrease in FEV1 (P = .026; 95% CI, −0.006 to −0.0004). For patient-reported outcomes, statistically significant worsening in both the European Organisation for Research and Treatment of Cancer Quality of Life Core Questionnaire (QLQ-C30 Version 3) and the lung module (QLQ-LC13) dyspnea scores occurred at the 18-month time point, but not earlier. No potential predictors of worsening dyspnea were statistically significant. There was no statistically significant decline in clinician-reported outcomes or global QoL scores. Conclusions We found a statistically significant decline in FEV1 at 18 months posttreatment. Smoking pack-years was a predictor for decline in diffusing capacity for carbon monoxide and FEV1 at 18 months. Worsening of patient-reported dyspnea scores was observed, consistent with the expected progression of lung comorbid disease. The aim of this study was to report pulmonary function tests (PFTs) and clinician-reported and patient-reported quality-of-life (QoL) outcomes on a cohort of patients with non-small cell lung cancer (NSCLC) treated with SABR. A total of 119 patients with NSCLC were treated with SABR in the prospective cohort SSBROC study of patients with T1-T2N0M0 NSCLC. PFTs and QoL measures were obtained at baseline pretreatment and at 6-month intervals. Here we report on the 6- to 18-month time points. Analysis of covariance (ANCOVA) methods adjusting for baseline analyzed potential predictors on outcomes of PFTs and patient-reported dyspnea at 18 months. The only statistically significant decline in PFTs was seen in forced expiratory volume in 1 second (FEV1) at 18 months post-SABR, with a decline of −0.11 L (P = .0087; 95% CI, −0.18 to −0.02). Of potential predictors of decline, only a 1-unit increase in smoking pack-years resulted in a −0.12 change in diffusing capacity for carbon monoxide (P = .026; 95% CI, −0.02 to −0.23) and a 0.003 decrease in FEV1 (P = .026; 95% CI, −0.006 to −0.0004). For patient-reported outcomes, statistically significant worsening in both the European Organisation for Research and Treatment of Cancer Quality of Life Core Questionnaire (QLQ-C30 Version 3) and the lung module (QLQ-LC13) dyspnea scores occurred at the 18-month time point, but not earlier. No potential predictors of worsening dyspnea were statistically significant. There was no statistically significant decline in clinician-reported outcomes or global QoL scores. We found a statistically significant decline in FEV1 at 18 months posttreatment. Smoking pack-years was a predictor for decline in diffusing capacity for carbon monoxide and FEV1 at 18 months. Worsening of patient-reported dyspnea scores was observed, consistent with the expected progression of lung comorbid disease.
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