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
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
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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