Service d'Oncologie Thoracique, Hôpital Bichat, AP-HP, Institut du Cancer AP-HP Nord, Paris, France.
Université Paris Cité, Inserm CIC-EC 1425, Paris, France.
Eur Respir J. 2024 May 2;63(5). doi: 10.1183/13993003.01809-2023. Print 2024 May.
Several rare surfactant-related gene (SRG) variants associated with interstitial lung disease are suspected to be associated with lung cancer, but data are missing. We aimed to study the epidemiology and phenotype of lung cancer in an international cohort of SRG variant carriers.
We conducted a cross-sectional study of all adults with SRG variants in the OrphaLung network and compared lung cancer risk with telomere-related gene (TRG) variant carriers.
We identified 99 SRG adult variant carriers ( (n=18), (n=31), (n=24), (n=14) and (n=12)), including 20 (20.2%) with lung cancer ( (n=7), (n=8), (n=3), (n=2) and (n=0)). Among SRG variant carriers, the odds of lung cancer was associated with age (OR 1.04, 95% CI 1.01-1.08), smoking (OR 20.7, 95% CI 6.60-76.2) and / variants (OR 3.97, 95% CI 1.39-13.2). Adenocarcinoma was the only histological type reported, with programmed death ligand-1 expression ≥1% in tumour cells in three samples. Cancer staging was localised (I/II) in eight (40%) individuals, locally advanced (III) in two (10%) and metastatic (IV) in 10 (50%). We found no somatic variant eligible for targeted therapy. Seven cancers were surgically removed, 10 received systemic therapy, and three received the best supportive care according to their stage and performance status. The median overall survival was 24 months, with stage I/II cancers showing better survival. We identified 233 TRG variant carriers. The comparative risk (subdistribution hazard ratio) for lung cancer in SRG patients TRG patients was 18.1 (95% CI 7.1-44.7).
The high risk of lung cancer among SRG variant carriers suggests specific screening and diagnostic and therapeutic challenges. The benefit of regular computed tomography scan follow-up should be evaluated.
几种与肺表面活性剂相关的基因(SRG)变异与间质性肺疾病相关,据推测这些变异也与肺癌有关,但目前数据尚缺。我们旨在对 SRG 变异携带者的国际队列进行研究,以探讨其流行病学和肺癌表型。
我们对 OrphaLung 网络中的所有成年人进行了 SRG 变异的横断面研究,并将其与端粒相关基因(TRG)变异携带者的肺癌风险进行了比较。
我们确定了 99 例成年 SRG 变异携带者( (n=18), (n=31), (n=24), (n=14) 和 (n=12)),其中 20 例 (20.2%)患有肺癌 ( (n=7), (n=8), (n=3), (n=2) 和 (n=0))。在 SRG 变异携带者中,肺癌的发病风险与年龄 (OR 1.04, 95% CI 1.01-1.08)、吸烟史 (OR 20.7, 95% CI 6.60-76.2) 和 / 变异 (OR 3.97, 95% CI 1.39-13.2) 相关。报告的组织学类型仅为腺癌,三个样本的肿瘤细胞中程序性死亡配体-1 的表达≥1%。8 例 (40%)患者的癌症分期为局限性 (I/II),2 例 (10%)为局部晚期 (III),10 例 (50%)为转移性 (IV)。我们未发现适合靶向治疗的体细胞变异。7 例癌症接受了手术切除,10 例接受了全身治疗,根据其分期和体能状态,3 例接受了最佳支持治疗。中位总生存期为 24 个月,I/II 期癌症的生存情况更好。我们确定了 233 例 TRG 变异携带者。SRG 患者与 TRG 患者的肺癌比较风险(亚分布危险比)为 18.1(95% CI 7.1-44.7)。
SRG 变异携带者的肺癌高风险提示存在特定的筛查、诊断和治疗挑战。应评估定期计算机断层扫描随访的获益。