Efficacy and Safety of Pirfenidone in CTD-ILD

Efficacy, Safety, Immune Function of Pirfenidone in the Treatment of Connetive Tissue Disease -Related Interstitial Lung Disease(CTD-LID)

A single-center randomized controlled study will be used to observe the efficacy and safety of pirfenidone on CTD-ILD patients for 24 months.

The main research endpoints is the lung function (FVC) at 6 months. The clinical dyspnea score, 6-minute walking distance, index of lung function and imaging indicators are evaluated, as well as primary disease activity and adverse reactions of therapy with glucocorticoid and immunosuppressants up to 24 months.

Study Overview

• Status: Recruiting
• Conditions: Connective Tissue Diseases; Interstitial Lung Disease; Pirfenidone
• Intervention / Treatment: Drug: Pirfenidone; Drug: glucocorticoid and immunosuppressant

Detailed Description

A total of 120 Chinese patients with connective tissue disease-associated interstitial lung disease (CTD-ILD), including inflammatory myopathy (IIM), rheumatoid arthritis (RA), systemic sclerosis (SSc), and other connective tissue diseases, will be enrolled to use Pirfenidone or not in this study according to 2:1 random entry. Glucocorticoid and immunosuppressants worked as background treatment.

The main research endpoint is the lung function (FVC) at 6 months. The clinical dyspnea score, 6-minute walking distance, lung function and imaging indicators, primary disease activity index are evaluated regularly until 24 months. The relationship of pirfenidone concentration, clinical effect and safety, immune function will be analyzed also.

• Study Type: Interventional
• Enrollment (Anticipated): 120
• Phase: Phase 4

Contacts and Locations

• Study Contact: Name: Qiang Shu, Dr; Phone Number: 0086-0531-82169654; Email: shuqiang@sdu.edu.cn
• Study Contact Backup: Name: keke xie; Phone Number: 0086-0531-82169654; Email: 695052518@qq.com

Study Locations

• China
  • Shandong
    • Jinan, Shandong, China, 250012
      • Recruiting
      • Qilu hospital
      • Contact: xiaoyun yang; Phone Number: +8653182169035; Email: qlyykyc@163.com

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

1. Age ≥18 years;
2. Meet several CTD diagnostic criteria (RA, IIM, SSc) and UCTD/IPAF classification criteria;
3. HRCT diagnosis confirmed interstitial lung disease (ILD) with corresponding clinical manifestations;
4. Patients who were able to complete vital capacity (FVC) or carbon monoxide dispersion (DLco) tests (with Hb correction).
5. Patients with clinical deterioration more than 1 month after diagnosis of ILD history, or poor response or intolerance to Glucocorticoids or immunosuppressants treatment, or poor response or intolerance to other antifibrotic drugs (acetyl hemitrine, nidanib, etc.), or effective use of PFD, and exacerbation of clinical symptoms or ILD indicators more than 3 months after withdrawal of the drug.
6. Poor response was defined as no improvement in one of the following:

(1) Symptoms of dyspnea such as cough, chest tightness, breathlessness, shortness of breath after activity, or decreased activity endurance;

(2) the worst decrease in oxygen saturation as measured by pulse oxygen saturation (SpO2) observed during 6MWD;

(3) There was no improvement in pulmonary ventilation (FVC%) or lung dispersion (DLco%);

(4) HRCT findings: new onset, fibrosis tendency or density of ILD lesions were not decreased;

Clinical deterioration was defined as meeting one of three criteria:

1. Clinical deterioration or dyspnea within 4 weeks;
2. New or worsening radiological abnormalities on chest X-ray or high-resolution CT;
3. Objective deterioration of pulmonary function tests or gas exchange, defined as meeting at least one of the following criteria:

1) Start long-term oxygen therapy or increase oxygen supplementation by at least 1 L/min to maintain resting oxygen saturation of at least 90%;

2) FVC decreased by more than 5% compared with the previously measured value; Or a decrease in DLCO of more than 10% from previous measurements; Or a 20% decrease in 6MWD from previous measurements.

7. If concomitant therapy with immunosuppressants was used, the dose was stable for at least 4 weeks before the baseline period. The types of immunomodulator hydroxychloroquine (HCQ) or immunosuppressive agents are MMF, TAC, JAKi, CTX, LEF, AzA, iguratimod etc.

8. Concomitant glucocorticoids: IIM patients with glucocorticoids dose (calculated as the equivalent dose of prednisone) ≤60mg/d and relatively stable disease; For other CTD patients, the glucocorticoids dose (calculated as prednisone equivalent dose) was ≤40mg/ day for at least 1 month.

Exclusion Criteria:

1. Subjects have systemic vasculitis, other arthritis other than CTD or RA such AS psoriatic arthritis, SPA, AS, SLE and pSS;

2. ILD patients with other obvious causes, such as HIV, GVHD, etc.

3. Patients with obvious abnormal combined organ function;

1. Liver :AST, ALT, R-GT, bilirubin at 1.5 ULN, or previously diagnosed viral hepatitis;
2. Kidney: creatinine clearance rate 30ml /min;
3. Lung: airway obstruction (pre-bronchodilator FEV1/FVC & LT; 0.7), pleural effusion accounted for more than 20% of pleural effusion, severe pulmonary infection or other clinically significant pulmonary abnormalities;
4. Cardiovascular: myocardial infarction within 6 months;
5. gastrointestinal tract: active peptic ulcer or bleeding;
6. Blood system: severe anemia, leukopenia, thrombocytopenia;
7. Nervous system: patients with mental disorders; Cerebral thrombotic events (stroke and transient ischemic attack) within the last 1 year;

4. Tuberculosis, cancer, hereditary diseases and other diseases with poor prognosis;

5. Effective contraception cannot be guaranteed during pregnancy, lactation or childbearing age;

6. Evidence of alcohol or drug abuse, according to the researchers;

7. Allergic to glucocorticoids, immunosuppressants and PFD;

8. Unable to complete regular follow-up and post-treatment pulmonary function tests;

9. PFD users not included in the efficacy analysis but included in the safety analysis: those who had used PFD for less than 3 months 6 months before the primary endpoint; The duration of use was less than 3 months before the 24th month of the syudy and the total duration of use was less than 6 months.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: pirfenidone group; CTD-ILD patients treated with pirfenidone、glucocorticoid and immunosuppressant.	Drug: Pirfenidone; Drug:pirfenidone CTD-ILD patients treated with pirfenidone up to the maximum tolerable dose Drug: glucocorticoid and immunosuppressant CTD-ILD patients treated with glucocorticoid and immunosuppressant according to the condition of the disease; Other Names: glucocorticoid and immunosuppressant; Drug: glucocorticoid and immunosuppressant; Drug: glucocorticoid and immunosuppressant CTD-ILD patients treated with glucocorticoid and immunosuppressant according to the condition of the disease
Active Comparator: No-pirfenidone group; CTD-ILD patients treated with glucocorticoid and immunosuppressant,without pirfebidone	Drug: glucocorticoid and immunosuppressant; Drug: glucocorticoid and immunosuppressant CTD-ILD patients treated with glucocorticoid and immunosuppressant according to the condition of the disease

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in FVC%	change in percentage of forced vital capacity (FVC) from 6 months to baseline	6 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in FVC %	change from baseline in percentage of forced vital capacity (FVC)	3months 12 months 24 months
change in FEV1%、DLco%、TLC%	change from baseline in carbon monoxide diffusing capacity (DLco)、FEV1、TLC	3months 6months 12months 24months
Proportion of patients and time with a decrease in DLco%	Percentage of patients and time with DLco% decreased>15% compared to baseline	3months 6months 12months 24months
Proportion of patients and time with a decrease in FVC%	Percentage of patients and time with FVC% decreased>10% compared to baseline	3months 6months 12months 24months
Progression-free survival	survival with a predicated absolute FVC% decrease of no more than 10% from baseline,and a predicated absolute DLco% decrease of no more than 15% from baseline	up to 24months
change in absolute value of FVC and DLco	absolute value change of FVC(ml) and DLco(ml) at each time point and annual decline rate compared with baseline	3months 6months 12months 24months
changes from baseline in 6 minutes walking distance	changes from baseline in 6 minutes walking distance	3months 6months 12months 24months
change in pulse oxygen saturation	the worst oxygen saturation as measured by pulse oxygen saturation(SpO2) was observed during 6 minutes walking distance	up to 24months
Worsening respiratory symptoms	Proportion of patients with worsening respiratory symptoms at each time point compared with baseline	3 months 6months 12months 24months
Advances in imaging	The proportion of patients with disease progression on imaging at each time point compared with baseline	3 months 6months 12months 24months
Imaging changes	changes from baseline in high-resolution computed tomography (HRCT)	6months 12months 24months
Borg dyspnea Index score	cChange of Borg dyspnea index score at each time point compared with baseline	3 months 6months 12months 24months
clinical deteriorration	The time and incidence of the first clinical deterioration ,Number of clinical exacerbations,Time between the all-cause deaths	up to 24months
Changes from baseline in C-reactive protein (CRP),Erythrocyte Sedimentation Rate(ESR),Inflammatory factors and indicators.	Changes from baseline in C-reactive protein (CRP),Erythrocyte Sedimentation Rate(ESR),Inflammatory factors and indicators.	3 months 6months 12months 24months
Changes from baseline in primary disease activity	Changes from baseline in primary disease activity	up to 24months
Adverse events , timing,type,extent,frequency,and outcome of SAE	Adverse events , timing,type,extent,frequency,and outcome of SAE	up to 24months
FVC% area under the curve	forced vital capacity (FVC)% area under the curve	3months 6months 12months 24months
Predicators of pirfenidone response in each disease subgroup	Predicators of pirfenidone response in each disease subgroup	3months 6months 12months 24months

Collaborators and Investigators

• Sponsor: Qilu Hospital of Shandong University
• Investigators: Principal Investigator: xiaoyun yang, Dr, Study Principal Investigator Qilu HOspital of Shandong Uniwersity

Study record dates

Study Major Dates

• Study Start (Actual): June 22, 2022
• Primary Completion (Anticipated): June 30, 2025
• Study Completion (Anticipated): December 1, 2025

Study Registration Dates

• First Submitted: August 16, 2022
• First Submitted That Met QC Criteria: August 16, 2022
• First Posted (Actual): August 17, 2022

Study Record Updates

• Last Update Posted (Actual): November 30, 2022
• Last Update Submitted That Met QC Criteria: November 27, 2022
• Last Verified: November 1, 2022

More Information

Terms related to this study

• Keywords: rheumatoid arthritis; interstitial lung disease; systemic sclerosis; connective tissue disease; pirfenidone; inflammatory myopathy
• Additional Relevant MeSH Terms: Respiratory Tract Diseases; Lung Diseases; Connective Tissue Diseases; Lung Diseases, Interstitial; Physiological Effects of Drugs; Peripheral Nervous System Agents; Analgesics; Sensory System Agents; Anti-Inflammatory Agents, Non-Steroidal; Analgesics, Non-Narcotic; Anti-Inflammatory Agents; Antirheumatic Agents; Antineoplastic Agents; Immunologic Factors; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists; Pirfenidone; Immunosuppressive Agents; Glucocorticoids
• Other Study ID Numbers: PFD-CTD-ILD QiluH

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No