Bongiolatti Stefano, Salvicchi Alberto, Rosi Elisabetta, Bargagli Elena, Mugnaini Giovanni, Gonfiotti Alessandro, Lavorini Federico, Spagnolo Paolo, Dell'Amore Andrea, Rea Federico, Voltolini Luca
Thoracic Surgery Unit, Careggi University Hospital, 50134 Florence, Italy.
Respiratory Medicine Unit, Careggi University Hospital, 50134 Florence, Italy.
Life (Basel). 2024 Nov 19;14(11):1506. doi: 10.3390/life14111506.
The surgical treatment of concomitant lung cancer in patients with idiopathic pulmonary fibrosis is challenging due to the risk of life-threatening complications such as acute exacerbation development in the perioperative period. Few studies have investigated the role of anti-fibrotic drugs in this setting. The aim of this multicenter retrospective study was to evaluate the incidence of acute exacerbation, according to Collard, after lung resection in patients affected by concomitant idiopathic pulmonary fibrosis and lung cancer who were or were not on antifibrotic treatment. Secondary outcomes included: 30 and 90-day mortality and an estimation of overall and disease-free survival.
The study population consisted of patients affected by idiopathic pulmonary fibrosis who received curative-intent lung surgery in three Italian academic centers between 2015 and 2022. Patients were divided into two groups based on whether they were on perioperative treatment with anti-fibrotic drugs (chronical or prophylactic use) or not. To define predictors of acute exacerbation, univariate and multivariable exact logistic regression analysis were performed. The Kaplan-Meier method with log-rank test was used to estimate survival.
During the study period, = 55 patients underwent lung resection for lung cancer, including 29 patients who were treated with antifibrotic agents. Although the sample size was small and few events were studied, the incidence of acute exacerbation was significantly lower among patient on anti-fibrotic therapy (3.4% vs. 23.1%, = 0.044); in addition, anti-fibrotic treatment was the strong factor preventing acute exacerbation at the multivariable analysis (OR 0.089, = 0.038). Post-operative 30- and 90-day mortality rates were not significantly lower in the anti-fibrotic treatment group (0% and 0% vs. 7.7% and 11.5%, = 0.21 and = 0.099, respectively). Overall and disease-free survival rates were similar.
Considering the limitations of this retrospective study with a small sample size, anti-fibrotic perioperative treatment was associated with reduced incidence of acute exacerbation. Based on these real-world data, this pathway could be proposed as a prophylactic treatment in patients with concomitant idiopathic pulmonary fibrosis and cancer undergoing lung resection.
特发性肺纤维化患者合并肺癌的外科治疗具有挑战性,因为围手术期存在发生危及生命并发症(如急性加重)的风险。很少有研究探讨抗纤维化药物在这种情况下的作用。这项多中心回顾性研究的目的是评估在接受或未接受抗纤维化治疗的特发性肺纤维化合并肺癌患者肺切除术后,根据科拉德标准确定的急性加重发生率。次要结局包括:30天和90天死亡率以及总生存期和无病生存期的估计。
研究人群包括2015年至2022年期间在三个意大利学术中心接受根治性肺手术的特发性肺纤维化患者。根据患者是否接受抗纤维化药物围手术期治疗(长期或预防性使用)分为两组。为了确定急性加重的预测因素,进行了单变量和多变量精确逻辑回归分析。采用Kaplan-Meier法和对数秩检验来估计生存期。
在研究期间,55例患者因肺癌接受了肺切除术,其中29例接受了抗纤维化药物治疗。尽管样本量小且研究的事件较少,但抗纤维化治疗组的急性加重发生率显著较低(3.4%对23.1%,P = 0.044);此外,在多变量分析中,抗纤维化治疗是预防急性加重的有力因素(OR 0.089,P = 0.038)。抗纤维化治疗组术后30天和90天死亡率没有显著降低(分别为0%和0%对7.7%和11.5%,P = 0.21和P = 0.099)。总生存期和无病生存期相似。
考虑到这项小样本回顾性研究的局限性,抗纤维化围手术期治疗与急性加重发生率降低相关。基于这些真实世界数据,对于接受肺切除术的特发性肺纤维化合并癌症患者,可将此方法作为一种预防性治疗方案。