About this trial
This study aims to evaluate the safety and efficacy of the umbilical cord blood mononuclear cells (UCB-MNCs) therapy for radiation-induced lung injuryr (RILI) by observing factors related to the therapeutic effect and adverse reactions of UCB-MNCs in treating RILI .
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Ages 18-75 years,with no restriction on gender;
History of chest radiotherapy;
Diagnosed with grade 2-3 radiation-induced lung injury according to CTCAE 4.0 classification criteria in "Diagnosis and Treatment of Radiation-induced Lung Injury";
Inadequate response to conventional treatment for two weeks, with no relief or progressive worsening of symptoms;
Disqualifiers
Severe cardiac insufficiency (such as NYHA class III or IV), uncontrolled hypertension (systolic blood pressure ≥160mmHg or diastolic blood pressure ≥110mmHg);
Positive for hepatitis B, hepatitis C, human immunodeficiency virus (HIV), or syphilis;
ECOG score ≥2;
Currently participating in or participated in other clinical trials within 4 weeks;
Trial design
Single group
Treatments tested in this trial
UCB-MNCs
Biological/VaccineUCB-MNCs were administered via intravenous infusion three times, once per week, with a dose of 3×10⁸ cells per infusion.
Treatment groups
Trial outcomes
Primary outcomes
Chest Enhanced CT Scan report
Evaluate changes in lung damage ,and calculate the change in total lesion volume as a percentage of total lung volume.
Secondary outcomes
Modified Medical Research Council Dyspnea Scale (mMRC Score)
mMRC Score is a subjective scale for assessing the severity of breathing difficulties,dyspnea is classified into five grades (0 to 4). The higher the grade, the more severe the symptoms and the more obvious the limitation of movement.
6-minute walking distance test(6MWT)
The 6-minute walking distance (6MWD) is a method for assessing a patient's cardiopulmonary function and exercise endurance by measuring the maximum distance they can walk as fast as possible within 6 minutes.
Change from baseline in forced expiratory volume in 1st second (FEV1)
FEV1 is the maximal volume of air that can be expired in 1st second of forced vital capacity maneuver using spirometry. We measured FEV1 at baseline and at 1、3 、6 months and 12 months after the last treatment.
Change from baseline in forced vital capacity (FVC)
Forced vital capacity (FVC) is the maximal volume of air that can be expired while patient performs forced expiration as fast and as deep as possible using spirometry. We measured FEV1 at baseline and at 1、3 、6 months and 12 months after the last treatment.
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: