Lower dose of Pirfenidone as effective as full dose for reducing disease progression in IPF
Written By : Aditi
Medically Reviewed By : Dr. Kamal Kant Kohli
Published On 2023-02-10 04:30 GMT | Update On 2023-02-10 07:49 GMT
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Korea: A study published in the Korean Journal of Internal Medicine has concluded that the pirfenidone effect for reducing the progression of idiopathic pulmonary fibrosis persists even at a lower dose in patients who cannot tolerate a standard full dose.
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive disease. The prognosis of the disease is extremely poor, with a median survival duration of 3 years from diagnosis.
Pirfenidone is an antifibrotic drug. As shown in large trials, Pirfenidone reduces the rate of decline in FVC and prolongs progression-free survival. The important consideration here is that it has effectiveness, slows down the IPF progression, and has adverse events.
The study points include the following:
- The study included 338 patients treated with Pirfenidone (July 2012 - March 2018).
- The researchers investigated demographics, pulmonary function, mortality, and adverse events.
- Comparing Forced Vital Capacity (FVC) and DLCO, diffusing capacity of the lungs for carbon monoxide changes before and after treatment with Pirfenidone was + 2.45 % and + 3.79 %. With standard and lower doses, individual values were + 2.13 %, + 3.65 % and, + 3.17 %, + 4.57 %, respectively.
- The total adverse event reported was 81.7 %.
- Nearly 24.6 % discontinued the treatment due to adverse events.
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