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Evaluation of 0.05% CsA and 0.1% FK506 Eye Drops in Ocular GVHD Treatment

Primary Purpose

Graft Versus Host Disease in Eye

Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Cyclosporine
tacrolimus
Sponsored by
Peking University Third Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Graft Versus Host Disease in Eye focused on measuring ocular graft-versus-host disease, dry eye, cyclosporine, tacrolimus, prospective study

Eligibility Criteria

4 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosed as chronic ocular GVHD
  • Did not receive eye local immunosuppressive therapy
  • Non pregnant patients

Exclusion Criteria:

  • Have a history of eye surgery in the past six months
  • Suffering from other eye diseases (autoimmune diseases, glaucoma, serious infection, retinopathy, allergy, cataract, eye trauma, etc.)
  • Hormones or immunosuppressants were used before enrollment

Sites / Locations

  • Peking University Third Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

cyclosporine group

tacrolimus group

Arm Description

The chronic ocular GVHD patients in cyclosporine group received local 0.05% cyclosporine 4 times/day for 3 months, and then changed to 0.05% cyclosporine for 2 times/day for 3 months

The chronic ocular GVHD patients in tacrolimus group received local 0.05% tacrolimus 2 times/day for 3 months, and then changed to 0.05% cyclosporine for 2 times/day for 3 months

Outcomes

Primary Outcome Measures

visual acuity
visual acuity
visual acuity
visual acuity
visual acuity
visual acuity
visual acuity
visual acuity
Intraocular pressure
Intraocular pressure
Intraocular pressure
Intraocular pressure
Intraocular pressure
Intraocular pressure
Intraocular pressure
Intraocular pressure
Ocular Surface Disease Index
Ocular Surface Disease Index
Ocular Surface Disease Index
Ocular Surface Disease Index
Ocular Surface Disease Index
Ocular Surface Disease Index
Ocular Surface Disease Index
Ocular Surface Disease Index
Corneal fluorescein staining
Corneal fluorescein staining
Corneal fluorescein staining
Corneal fluorescein staining
Corneal fluorescein staining
Corneal fluorescein staining
Corneal fluorescein staining
Corneal fluorescein staining
Tear break-up time
Tear break-up time
Tear break-up time
Tear break-up time
Tear break-up time
Tear break-up time
Tear break-up time
Tear break-up time

Secondary Outcome Measures

Full Information

First Posted
February 7, 2022
Last Updated
March 14, 2022
Sponsor
Peking University Third Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05294666
Brief Title
Evaluation of 0.05% CsA and 0.1% FK506 Eye Drops in Ocular GVHD Treatment
Official Title
Evaluation of Efficacy, Safety and Tolerability of 0.05% Cyclosporine and 0.1% Tacrolimus Eye Drops in the Treatment of Chronic Ocular Graft-versus-host Disease
Study Type
Interventional

2. Study Status

Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
April 1, 2020 (Actual)
Primary Completion Date
June 1, 2021 (Actual)
Study Completion Date
July 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Peking University Third Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
It is planned to explore the efficacy and safety of local 0.05% cyclosporine eye drops in the treatment of chronic graft-versus-host eye disease. Through the comparative study with 0.1% tacrolimus eye drops, to clarify the short-term and long-term efficacy of 0.05% CSA in these patients, and to explore the benefits of long-term maintenance of local cyclosporine to patients.
Detailed Description
Chronic graft-versus-host disease (GVHD) is a common and serious complication after allogeneic hematopoietic stem cell transplantation. Its clinical presentation is similar to that of an autoimmune disease and can affect many organs, including the skin, liver, gastrointestinal tract, lungs and eyes. Ocular GVHD occurs in 30-60% of patients undergoing hematopoietic stem cell transplantation and 60-90% of patients with other systemic GVHD. Chronic ocular GVHD usually occurs 9-24 months after hematopoietic stem cell transplantation and mainly affects the cornea, conjunctiva, lacrimal gland, eyelid and meibomian gland, and leads to inflammation and fibrosis of these tissues. The characteristic manifestations of chronic GVHD include dry keratoconjunctivitis, cicatric conjunctivitis, punctate keratopathy, corneal ulcer and perforation. Severe dry eye is the most common manifestation of ocular GVHD. Patients have burning sensation, foreign body sensation, photophobia, dry eye, itching and other symptoms. This is associated with reduced tear secretion due to damage to the lacrimal gland as well as with goblet cell loss and tear film instability due to meibomian gland dysfunction. Chronic eye GVHD has the potential to cause severe visual impairment and significantly reduce the patient's quality of life. The principle of topical treatment of ocular GVHD is to lubricate the ocular surface, reduce ocular surface inflammation, prevent tear evaporation, and promote epithelial repair. Specific local treatment options include glucocorticoids, immunosuppressants, growth factors and artificial tears. Local glucocorticoids are the first-line treatment at the present stage, but the side effects of hormone therapy are relatively large. Long-term use can lead to damaged epithelial formation, thinning of the cornea, increased intraocular pressure, cataract, infectious keratitis, etc. Therefore, it is necessary to closely monitor the treatment period and minimize the use time. At present, the most commonly used topical immunosuppressants are tacrolimus (FK506) and cyclosporine (CsA). Both belong to calcineurin inhibitors, which can inhibit the activation of calcium-dependent T cells, thus exerting immunosuppressive effect. 0.05% CsA is an eye drop mainly used for the treatment of moderate and severe dry eye, with good therapeutic effect and tolerability [18-23], but slow onset of effect. In the treatment of patients with chronic ocular GVHD, previous studies have shown that cyclosporine eye drops can improve patients' dry eye symptoms, reduce corneal fluorescence staining, and increase tear film rupture time. However, the number of clinical studies on the treatment of chronic ocular GVHD with 0.05% CsA eye drops is limited, with a small number of patients enrolled and relatively short follow-up time. The immunosuppressive effect of tacrolimus is significantly higher than cyclosporine, which is 100 times higher than reported in literature. Therefore, tacrolimus is mainly used for the treatment of rejection after corneal transplantation and immune-related ocular surface diseases. What is the efficacy and tolerability of such a powerful immunosuppressant in treating GVHD? There are few literature reports, but long-term ocular application can reduce local immunity and increase the risk of local infection. At the same time, tacrolimus is very irritating, and some patients cannot tolerate it and choose to stop using the drug. At present, there is still a lack of clinical evidence to compare the efficacy of cyclosporine and tacrolimus eye drops in patients with chronic ocular GVHD. Therefore, by comparing the effectiveness, safety and tolerance of 0.05% CsA eye drops and 0.1% tacrolimus eye drops in the treatment of chronic eye graft-versus host eye disease, this study aims to explore a reasonable treatment plan for chronic eye GVHD and provide theoretical basis for clinical application.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Graft Versus Host Disease in Eye
Keywords
ocular graft-versus-host disease, dry eye, cyclosporine, tacrolimus, prospective study

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
89 (Actual)

8. Arms, Groups, and Interventions

Arm Title
cyclosporine group
Arm Type
Experimental
Arm Description
The chronic ocular GVHD patients in cyclosporine group received local 0.05% cyclosporine 4 times/day for 3 months, and then changed to 0.05% cyclosporine for 2 times/day for 3 months
Arm Title
tacrolimus group
Arm Type
Experimental
Arm Description
The chronic ocular GVHD patients in tacrolimus group received local 0.05% tacrolimus 2 times/day for 3 months, and then changed to 0.05% cyclosporine for 2 times/day for 3 months
Intervention Type
Drug
Intervention Name(s)
Cyclosporine
Other Intervention Name(s)
CsA
Intervention Description
The chronic ocular GVHD patients in cyclosporine group received local 0.05% cyclosporine 4 times/day for 3 months, and then changed to 0.05% cyclosporine for 2 times/day for 3 months
Intervention Type
Drug
Intervention Name(s)
tacrolimus
Other Intervention Name(s)
FK506
Intervention Description
The chronic ocular GVHD patients in tacrolimus group received local 0.05% tacrolimus 2 times/day for 3 months, and then changed to 0.05% cyclosporine for 2 times/day for 3 months
Primary Outcome Measure Information:
Title
visual acuity
Description
visual acuity
Time Frame
Within 4 hours of initial enrollment
Title
visual acuity
Description
visual acuity
Time Frame
At the first month of enrollment
Title
visual acuity
Description
visual acuity
Time Frame
At the third month of enrollment
Title
visual acuity
Description
visual acuity
Time Frame
At the sixth month of enrollment
Title
Intraocular pressure
Description
Intraocular pressure
Time Frame
Within 4 hours of initial enrollment
Title
Intraocular pressure
Description
Intraocular pressure
Time Frame
At the first month of enrollment
Title
Intraocular pressure
Description
Intraocular pressure
Time Frame
At the third month of enrollment
Title
Intraocular pressure
Description
Intraocular pressure
Time Frame
At the sixth month of enrollment
Title
Ocular Surface Disease Index
Description
Ocular Surface Disease Index
Time Frame
Within 4 hours of initial enrollment
Title
Ocular Surface Disease Index
Description
Ocular Surface Disease Index
Time Frame
At the first month of enrollment
Title
Ocular Surface Disease Index
Description
Ocular Surface Disease Index
Time Frame
At the third month of enrollment
Title
Ocular Surface Disease Index
Description
Ocular Surface Disease Index
Time Frame
At the sixth month of enrollment
Title
Corneal fluorescein staining
Description
Corneal fluorescein staining
Time Frame
Within 4 hours of initial enrollment
Title
Corneal fluorescein staining
Description
Corneal fluorescein staining
Time Frame
At the first month of enrollment
Title
Corneal fluorescein staining
Description
Corneal fluorescein staining
Time Frame
At the third month of enrollment
Title
Corneal fluorescein staining
Description
Corneal fluorescein staining
Time Frame
At the sixth month of enrollment
Title
Tear break-up time
Description
Tear break-up time
Time Frame
Within 4 hours of initial enrollment
Title
Tear break-up time
Description
Tear break-up time
Time Frame
At the first month of enrollment
Title
Tear break-up time
Description
Tear break-up time
Time Frame
At the third month of enrollment
Title
Tear break-up time
Description
Tear break-up time
Time Frame
At the sixth month of enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed as chronic ocular GVHD Did not receive eye local immunosuppressive therapy Non pregnant patients Exclusion Criteria: Have a history of eye surgery in the past six months Suffering from other eye diseases (autoimmune diseases, glaucoma, serious infection, retinopathy, allergy, cataract, eye trauma, etc.) Hormones or immunosuppressants were used before enrollment
Facility Information:
Facility Name
Peking University Third Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100000
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Evaluation of 0.05% CsA and 0.1% FK506 Eye Drops in Ocular GVHD Treatment

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