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达那唑治疗对晚期特发性肺纤维化患者无效。

No effect of danazol treatment in patients with advanced idiopathic pulmonary fibrosis.

作者信息

Hoffman Thijs W, van Moorsel Coline H M, van der Vis Joanne J, Biesma Douwe H, Grutters Jan C

机构信息

Interstitial Lung Diseases Center of Excellence, Department of Pulmonology, St Antonius Hospital, Nieuwegein, The Netherlands.

Department of Clinical Chemistry, St Antonius Hospital, Nieuwegein, The Netherlands.

出版信息

ERJ Open Res. 2023 Sep 25;9(5). doi: 10.1183/23120541.00131-2023. eCollection 2023 Sep.

Abstract

BACKGROUND

Telomere dysfunction can underly the development of idiopathic pulmonary fibrosis (IPF), and recent work suggests that patients with telomere syndromes might benefit from treatment with androgens, such as danazol.

METHODS

This was a prospective observational cohort study. 50 patients with IPF received off-label treatment with danazol after they showed progressive disease under treatment with pirfenidone or nintedanib. The primary outcome was the difference in yearly decline in forced vital capacity (FVC) prior to (pre) and after (post) start of treatment with danazol.

RESULTS

There was no significant difference in FVC-decline between 1 year pre and 1 year post start of danazol treatment (mean decline pre 395 mL (95% confidence interval (CI) 290-500) compared to post 461 mL (95% CI 259-712); p=0.46; paired t-test). 11 patients (22%) were still on danazol after 1 year, and 39 patients had stopped danazol, mainly because of side-effects (56%) or death (33%). In patients who were still using danazol after 1 year, FVC-decline significantly slowed down under danazol treatment (mean pre 512 mL (95% CI 308-716) post 198 mL (95% CI 16-380); p=0.04). Median survival post danazol was 14.9 months (95% CI 11.0-18.8).

CONCLUSION

Danazol as a treatment of last resort in patients with IPF did not lead to slowing of lung function decline and was associated with significant side-effects. It remains to be determined if earlier treatment or treatment of specific patient subgroups is beneficial.

摘要

背景

端粒功能障碍可能是特发性肺纤维化(IPF)发病的基础,最近的研究表明,患有端粒综合征的患者可能从雄激素治疗中获益,如达那唑。

方法

这是一项前瞻性观察队列研究。50例IPF患者在接受吡非尼酮或尼达尼布治疗后病情仍进展,接受了达那唑的非标签治疗。主要结局是开始使用达那唑治疗前(pre)和治疗后(post)1年用力肺活量(FVC)的年下降差异。

结果

开始使用达那唑治疗前1年和治疗后1年FVC下降无显著差异(治疗前平均下降395 mL(95%置信区间(CI)290 - 500),治疗后为461 mL(95% CI 259 - 712);p = 0.46;配对t检验)。1年后,11例患者(22%)仍在使用达那唑,39例患者已停用达那唑,主要原因是副作用(56%)或死亡(33%)。在1年后仍在使用达那唑的患者中,达那唑治疗期间FVC下降显著减缓(治疗前平均512 mL(95% CI 308 - 716),治疗后为198 mL(95% CI 16 - 380);p = 0.04)。达那唑治疗后的中位生存期为14.9个月(95% CI 11.0 - 18.8)。

结论

达那唑作为IPF患者的最后治疗手段,并未导致肺功能下降减缓,且伴有显著副作用。早期治疗或特定患者亚组的治疗是否有益仍有待确定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38d4/10518878/d4c7ac61593c/00131-2023.01.jpg

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