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Utility of nintedanib for severe idiopathic pulmonary fibrosis: a single-center retrospective study [Letter]

Authors Orsatti L, Fortea J, Quaresma M

Received 10 November 2018

Accepted for publication 10 February 2019

Published 12 April 2019 Volume 2019:13 Pages 1177—1178

DOI https://doi.org/10.2147/DDDT.S194065

Checked for plagiarism Yes

Review by Single-blind

Peer reviewer comments 3

Editor who approved publication: Dr Qiongyu Guo


Leticia Orsatti, Josep Fortea, Manuel Quaresma

Boehringer Ingelheim International GmbH, Ingelheim, Germany

We read with interest the study by Abe et al on the clinical utility of nintedanib in patients with severe idiopathic pulmonary fibrosis (IPF).1 Based on the retrospective follow-up of 51 patients, the authors concluded that the survival benefit from nintedanib is reduced among patients with severe IPF (n=17) compared with those with mild-to-moderate IPF (n=34), but that the prognosis for patients with severe IPF is significantly better in those who remain on nintedanib for more than 3 months.
In our opinion, the study design does not allow conclusions to be drawn about the treatment effect of nintedanib on survival in patients with severe versus mild-tomoderate IPF.

View the original paper by Abe and colleagues

A Letter to the Editor has been received and published for this article.



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