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Efficacy of Doxycycline in the Treatment of Early Stages of Mycosis Fungoides

Primary Purpose

Lymphoma

Status
Unknown status
Phase
Phase 3
Locations
Egypt
Study Type
Interventional
Intervention
Vibramycin
Phototherapy
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lymphoma focused on measuring Mycosis fungoides, Doxycycline

Eligibility Criteria

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

Inclusion Criteria:

  • Adults (above 18) of either sex with established diagnosis of classic MF

Exclusion Criteria:

  • Any variant of MF other than the classic variant.
  • Advanced stages of classic MF: Stage IIb, III or IV.
  • Pregnant and lactating females.
  • Patients with autoimmune diseases e.g. SLE
  • Patients with solid or hematological malignancies e.g. breast cancer, leukemia, etc.
  • Patients with any contraindications for doxycycline (eg: liver disease, kidney disease, photosensitivity, peptic ulcer or patients receiving systemic retinoids).
  • Patients with any contraindication to phototherapy (eg: any other skin cancers or photosensitivity); or to psoralen (eg: liver disease)

Sites / Locations

  • Dermatology departementRecruiting
  • Dermatology departmentRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Doxycyline

Phototherapy

Arm Description

Oral Vibramycin antibiotic100 mg capsule every 12 hours for 3 months

UVA+ psoralen 3 sessions per week for 3 months

Outcomes

Primary Outcome Measures

Clinical assessment
Clinical assessment of the extent of the lesions in body surface area

Secondary Outcome Measures

Pathological assessment
Pathological assessment using immunohistochemistry

Full Information

First Posted
September 5, 2017
Last Updated
August 22, 2018
Sponsor
Cairo University
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1. Study Identification

Unique Protocol Identification Number
NCT03454945
Brief Title
Efficacy of Doxycycline in the Treatment of Early Stages of Mycosis Fungoides
Official Title
Efficacy of Doxycycline in the Treatment of Early Stages of Mycosis Fungoides: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2017 (Actual)
Primary Completion Date
April 1, 2019 (Anticipated)
Study Completion Date
April 1, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Current study aims at assessing the efficacy of doxycycline as a potential treatment modality for early stages of MF.
Detailed Description
Objectives Objective is to evaluate the efficacy of doxycycline in treatment of early stages of mycosis fungoides (IA, IB and IIA) and to assess its apoptotic enhancing effect by studying the expression of BCL2 by the T lymphocytes. Study Design Randomized controlled trial Population of study & disease condition 30 patients with early stage mycosis fungoides (Stage Ia,Ib and IIa) Methodology in details After signing an informed consent, each participant will be subjected to: I. Baseline evaluation: Baseline biopsy to document the current state of the disease and to assess immunohistochemically the expression of CD3 and Bcl2 by the lymphocytes. Detailed history taking including onset, course, duration of the disease and history of any previous treatments used. Detailed examination of skin lesions and scoring using: Modified Severity of Index Weighted Assessment (mSWAT) Composite Assessment of Index Lesion Severity (CAILS) Pruritus scoring using a visual analog scale from 0-10, where 0=no pruritus and 10=worst imaginable pruritus Photography II. Treatment and dosing protocol: Participants will be randomly allocated in either one of the treatment groups: Group A: Will receive oral doxycycline in a dose of 200 mg daily for three months. Group B: Will receive PUVA with dosing & increments according to the standard protocols of the Phototherapy Unit, Dermatology Department, Cairo University; 3 sessions per week for 3 months. III. Timings of follow up visits and clinical assessments done: Patients will be regularly assessed at weeks 4, 8, and 12. Patients continuing for another three months, as mentioned above, will be assessed at weeks 16, 20 and 24. The following will be done at these follow up visits: mSWAT, CAILS, pruritus scoring and photography. Side effects will be monitored and managed accordingly. IV. Follow up biopsies: A repeat biopsy will be taken at initial improvement in CAILS (or at week 12) for immunohistochemical re-assessment of the expression of CD3 and Bcl2 by the lymphocytes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphoma
Keywords
Mycosis fungoides, Doxycycline

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Doxycyline
Arm Type
Experimental
Arm Description
Oral Vibramycin antibiotic100 mg capsule every 12 hours for 3 months
Arm Title
Phototherapy
Arm Type
Active Comparator
Arm Description
UVA+ psoralen 3 sessions per week for 3 months
Intervention Type
Drug
Intervention Name(s)
Vibramycin
Other Intervention Name(s)
Doxy
Intervention Description
Antibiotic
Intervention Type
Device
Intervention Name(s)
Phototherapy
Intervention Description
UVA+Psoralen
Primary Outcome Measure Information:
Title
Clinical assessment
Description
Clinical assessment of the extent of the lesions in body surface area
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Pathological assessment
Description
Pathological assessment using immunohistochemistry
Time Frame
3months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults (above 18) of either sex with established diagnosis of classic MF Exclusion Criteria: Any variant of MF other than the classic variant. Advanced stages of classic MF: Stage IIb, III or IV. Pregnant and lactating females. Patients with autoimmune diseases e.g. SLE Patients with solid or hematological malignancies e.g. breast cancer, leukemia, etc. Patients with any contraindications for doxycycline (eg: liver disease, kidney disease, photosensitivity, peptic ulcer or patients receiving systemic retinoids). Patients with any contraindication to phototherapy (eg: any other skin cancers or photosensitivity); or to psoralen (eg: liver disease)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hagar El Sayed, Master
Phone
01061248365
Email
hgr_ntr@yahoo.com
First Name & Middle Initial & Last Name or Official Title & Degree
Suzan Shalaby, MD
Phone
01224019459
Email
suzyandnls@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mona AbdEl Halim, MD
Organizational Affiliation
Cairo University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dermatology departement
City
Cairo
ZIP/Postal Code
11562
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hagar El Sayed, MD
Phone
01051248365
Email
hgr_ntr@yahoo.com
First Name & Middle Initial & Last Name & Degree
Suzan Shalaby, MD
Phone
01224019459
Email
suzyandnls@gmail.com
Facility Name
Dermatology department
City
Cairo
ZIP/Postal Code
11562
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hagar El Sayed, Master
Phone
01061248365
Email
hgr_ntr@yahoo.com
First Name & Middle Initial & Last Name & Degree
Suzan Shalaby, MD
Phone
01224019459
Email
suzyandnls@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32632956
Citation
Valipour A, Jager M, Wu P, Schmitt J, Bunch C, Weberschock T. Interventions for mycosis fungoides. Cochrane Database Syst Rev. 2020 Jul 7;7(7):CD008946. doi: 10.1002/14651858.CD008946.pub3.
Results Reference
derived
PubMed Identifier
31526286
Citation
El Sayed H, Shalaby S, Abdel-Halim MRE, Aboelfadl DM, Samir N. Efficacy of doxycycline in the treatment of early stages of mycosis fungoides: a randomized controlled trial. J Dermatolog Treat. 2021 Jun;32(4):424-431. doi: 10.1080/09546634.2019.1667474. Epub 2019 Sep 20.
Results Reference
derived

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Efficacy of Doxycycline in the Treatment of Early Stages of Mycosis Fungoides

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