Randomized Controlled Trial of Hydroxychloroquine Combined With Low-dose Corticosteroid in Pulmonary Sarcoidosis (QUIDOSE)
Pulmonary Sarcoidosis
About this trial
This is an interventional treatment trial for Pulmonary Sarcoidosis focused on measuring Sarcoidosis, Hydroxychloroquine, Pulmonary, Quality of life, Steroids
Eligibility Criteria
Inclusion Criteria:
- Age between 18-80 years old
- Pulmonary sarcoidosis meeting the diagnostic criteria form ATS 2020 AJRCCM diagnostic criteria.
- Patient with radiographic stage II (mediastinal-hilar bilateral lymphadenopathy and parenchymal involvement) or III (involvement pulmonary parenchymatous) and FVC<80% and respiratory symptom(s) among the following: cough, dyspnea, chest pain).
- Effective contraception for women of childbearing ages
- Informed consent signed.
- Affiliation to the social security system
Exclusion Criteria:
- Severe impairment requiring an immediate and urgent result and/or high doses of corticosteroids (neurological, cardiac, ophthalmic (severe uveitis with ocular sequala), laryngeal, nasosinusal, renal, severe hypercalcemia)
- Cardiomyopathy with heart failure
- Presence of other conditions that may influence respiratory function: COPD, Asthma, Obesity (BMI>30) pulmonary fibrosis disease, pulmonary neoplasia;
- Contraindication to hydroxychloroquinehypersensitivity to active substances or to excipients, retinopathy or severe cataract, or unilateral blindness, QTc prolongation, exposure to known treatments to prolong QT)
- Tamoxifen use
- Renal insufficiency with clearance <60ml/min
- History of retinopathy or maculopathy
- Contraindication to corticosteroid therapy (hypersensitivity of active substancies, infections and progressive virosis, glaucoma, psychotic state not controlled by treatment, live vaccine, uncontrolled diabetes mellitus and hypertension)
- Intermittent porphyria (risk of acute porphyria crisis)
- Glucose-6-Phosphate Dehydrogenase deficiency
- Seropositivity to HIV, HBV, HCV
- Systemic corticosteroid therapy or immunosuppressive therapy for at least 7 days in the previous year;
- History of treatment with hydroxychloroquine for sarcoidosis;
- Current pregnancy,
- Breastfeeding,
- Patient unable to answer questionnaires despite the presence of a caregiver.
- Patient under trustee
- Patient under legal protection
- Participation in another therapeutic interventional trial within 6 months of inclusion
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Hydroxychloroquine+low-dose prednisone
Medium-dose prednisone
Hydroxychloroquine, tablets, 400mg/day for 6 months combined with Prednisone, 20mg/day for 1 month, then 10mg/day for 20 weeks (ie up to M6). The cumulative doses of prednisone during the 6 months of the study will be 1820mg
"prednisone, tablets, 40mg/day for 4 weeks, then 30mg/day for 2 weeks, then 20mg/day for 2 weeks, then 15mg/day for 2 weeks, then 10mg/day for 14 weeks (i.e. up to M6). The cumulative doses of prednisone during the 6 months of the study will be 2870mg "