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CTCL Directed Therapy

CTCL Directed Therapy

Status
UNKNOWN
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03116659
Enrollment
8
Registered
2017-04-17
Start date
2018-02-01
Completion date
2020-12-30
Last updated
2019-08-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lymphoma, T-Cell, Cutaneous

Brief summary

Cutaneous lymphomas are rare cancers of lymphocytes (white blood cells) that involve the skin. Mycosis Fungoides (MF) is the most common type of Cutaneous T-cell lymphoma (CTCL) that typically presents with red, scaly patches that often mimic eczema or chronic dermatitis. The incidence of MF is about 1/100,000. Skin lesions tend to appear before the diagnosis of CTCL is made by several years. Early skin lesions may look like any dermatitis, eczema, or psoriasis, leading to delays in the diagnosis. Inflammation secondary to bacterial infection is thought to contribute to the T-cell proliferation in this type of cutaneous T-cell lymphoma. Antibiotic use for other purposes has shown to reduce the inflammation and size of lesions in CTCL patients. There has been limited studies with the use of antibiotics as direct treatment for this cancer. Host immunity is important in decreasing cancer development and progression. Imiquimod is a molecule that stimulates host immunity to reduce the progression of CTCL. There is strong evidence of clinical efficacy such that the National Comprehensive Cancer Network (NCCN) guidelines recommend Imiquimod for CTCL. Imiquimod is available in generic form, making it unlikely to be registered specifically for CTCL, despite its efficacy. Additionally, imiquimod is considered a first line treatment according to National Comprehensive Cancer Network (NCCN) guidelines for the treatment of Mycosis Fungoides. There are currently no studies that have been published that address treating CTCL patients with a combined approach of 1) decreasing inflammation caused by bacterial with antibiotics, and 2) enhancing the host immune system to destroy cancer cells. Our theory is if we treat patient with 14days of antibiotics and 30 days of Imiquimod there will be significant reduction in skin lesions.

Interventions

DRUGDoxycycline

Doxycycline 100 mg PO BID x 14 days

DRUGImiquimod

up to 2 packs 3/ week x 28 days

Sponsors

James J. Peters Veterans Affairs Medical Center
Lead SponsorFED

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 89 Years
Healthy volunteers
No

Inclusion criteria

* Patients age 30 - 89 years old * Stages I to II CTCL patients * Normal renal function, Cr ≤ 1.5

Exclusion criteria

* Aggressively progressing CTCL * Active infection and/or concurrent malignancy * Poor renal function (Cr \> 1.5) * Pregnancy (HCG serum +) * History of bone marrow suppression, MDS, anemia (Hemoglobin \< 8), thrombocytopenia (\< 50,000) or neutropenia (ANC \< 1500) * CHF, MI within last 6 months * Endocarditis * Allergies to Imiquimod or doxycycline

Design outcomes

Primary

MeasureTime frameDescription
Pilot assessment of response.1 yearPilot assessment of response assessed by decreased size or surface change of the 5 lesions

Countries

United States

Contacts

Primary ContactAli Dana, MD
Ali.Dana@VA.gov718-584-9000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026