Study on Safety and Efficacy of UCB-MNCs for Radiation-induced Lung Injury

Trial statusNot yet recruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
Age18-75
SponsorZhejiang Cancer Hospital

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 volunteers

Qualifiers

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

Design model

Single group

Treatments tested in this trial

  • UCB-MNCs

    Biological/Vaccine

    UCB-MNCs were administered via intravenous infusion three times, once per week, with a dose of 3×10⁸ cells per infusion.

Treatment groups

10 Participants
are divided into 1 treatment group
Group A: UCB-MNCsExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
Baseline and at 1、3、6 and 12 months after the last treatment.

Secondary outcomes

1

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.

Time frame
Baseline and at 1、3 、6 and 12 months after the last treatment.
2

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.

Time frame
Baseline and at 1、3 、6 and 12 months after the last treatment.
3

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.

Time frame
We measured FEV1 at baseline and at 1、3 、6 months and 12 months after the last treatment.
4

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.

Time frame
We measured FVC at baseline and at 1、3 、6 months and 12 months after the last treatment.

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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