Long-term Assessment of Chlormethine Gel in Mycosis Fungoides

Last updated: July 1, 2025
Sponsor: Fondazione Italiana Linfomi - ETS
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Non-hodgkin's Lymphoma

Cutaneous T-cell Lymphoma

Mycosis Fungoides

Treatment

N/A

Clinical Study ID

NCT07046663
FIL_CLOR-CTCL
  • Ages > 18
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

The study aims to provide comprehensive insights into the long-term therapeutic outcomes, potential adverse effects, and overall patient experience with chlormethine gel, thereby informing clinical practice and guiding future treatment strategies for mycosis fungoides.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients age ≥ 18

  • Histologically confirmed diagnosis of MF based on WHO Classification of Tumours,Haematolymphoid Tumours, 5th edition

  • Patients who are capable of understanding and willing, and able to read and write inItalian

  • Patients who have signed informed consent form

  • Patients who started treatment with chlormethine gel, from September 1, 2019 toSeptember 30, 2024.

  • Patients must have a minimum follow-up period of 6 months following the initiationof chlormethine treatment.

  • Availability of complete medical records in order to provide protocol requiredvariables.

Exclusion

Exclusion Criteria:

  • Patients for whom retrospective data or information on the type of therapy,duration, and clinical outcomes are not available in the center's medical records.

  • Refuse to sign a written informed consent.

  • Patients not meeting the above-mentioned inclusion criteria

Study Design

Total Participants: 190
Study Start date:
September 01, 2025
Estimated Completion Date:
June 30, 2026

Study Description

Primary cutaneous lymphomas (PCLs) are a rare group of lymphoproliferative disorders with neoplastic lymphocyte proliferation in the skin. Cutaneous T-cell lymphomas (CTCL) make up 75% of PCLs, with mycosis fungoides (MF) being the most common. The cause of MF is unclear, but persistent antigenic stimulation and chronic inflammation may lead to neoplastic transformation. Pathogenesis involves genetic and epigenetic abnormalities, with a crucial role played by the skin microenvironment. Data from the International PROCLIPI registry (PROspective Cutaneous Lymphoma International Prognostic Index Validation and Evaluation) provide insight into the clinical management and outcomes of CTCL. This study has confirmed that early-stage disease has a relatively favorable prognosis, with a 5-year survival rate of about 90% for stage IA patients. Treatment is stage-dependent. Early stages are managed with skin-directed therapies (topical steroids, chlormethine and phototherapy) as first lines, while refractory or advanced disease requires systemic therapies such as interferon, bexarotene, and extracorporeal photopheresis. Chemotherapy and new monoclonal agents are used for refractory advanced cases. Topical chlormethine (TC) is an alkylating agent successfully used in treating CTCL since the 1950s. It works by a cytotoxic mechanism on DNA, altering the growth of neoplastic cells and enhancing the host's immunogenic potential. Initially, TC was packaged in an aqueous solution, but its use was limited by a high rate of skin hypersensitivity. In 2013, a multicenter, randomized, blinded phase II study compared 0.02% TC ointment with 0.02% TC gel, demonstrating the gel's non-inferiority to the ointment. The study also recorded longer and faster responses in the gel arm. No detectable systemic absorption of the drug was observed in patients' blood, consistent with previous case series. The evidence on the development of secondary neoplasms is controversial, particularly the risk of non-melanoma skin cancers (NMSC), which ranges from 0 to 9%. This risk is higher in patients previously treated with other modalities known to increase skin cancer incidence (e.g., radiotherapy and phototherapy). Melanoma development was reported by Ramsay et al. in a single patient with Fitzpatrick type I skin and a history of NMSC.

Real-world data from numerous studies have confirmed the efficacy of TC gel in treating early-stage MF and its use in combination with systemic therapies for advanced stages. In particular, the PROVE study, based on US real-world experience, demonstrated that modulating the TC schedule to every other day maintained good efficacy while reducing the incidence of adverse events, such as irritant contact dermatitis (ICD), and improving patient compliance. In a previous retrospective study on the first patients treated with TC gel in Italy, was showed that hyperpigmentation correlates with good response.

Currently, there is a lack of data on long-term response, recurrence rates after initial response, and the effect on treated areas considering the significant irritative response.

Connect with a study center

  • AOU Ospedali Riuniti - Clinica di Ematologia

    Ancona,
    Italy

    Site Not Available

  • SC Dermatologia, ASST-Papa Giovanni XXIII,

    Bergamo,
    Italy

    Site Not Available

  • UO Dermatologia - IRCCS Policlinico S.Orsola-Malpighi

    Bologna,
    Italy

    Site Not Available

  • UO Dermatologia ASST Spedali Civili Brescia

    Brescia,
    Italy

    Site Not Available

  • UOC di Dermatologia - Azienda Ospedaliero-Universitaria di Cagliari, presidio Ospedaliero S. Giovanni di Dio

    Cagliari,
    Italy

    Site Not Available

  • UOC Dermatologia - Azienda Ospedaliero Universitaria Policlinico "G. Rodolico - San Marco"

    Catania,
    Italy

    Site Not Available

  • UOC Ematologia - ARNAS Nuovo Ospedale Garibaldi Nesima

    Catania,
    Italy

    Site Not Available

  • S.C. Dermatologia, AUSL Toscana Centro e Università degli Studi di Firenze, Presidio Ospedaliero Palagi

    Firenze,
    Italy

    Site Not Available

  • SC Dermatologia, Ente Ospedaliero Ospedali Galliera di Genova

    Genova,
    Italy

    Site Not Available

  • UO Dermatologia, ASST-Lecco, Azienda Ospedaliera A. Manzoni

    Lecco,
    Italy

    Site Not Available

  • UO Dermatologia Clinica - IRCCS Ospedale San Raffaele di Milano

    Milano,
    Italy

    Site Not Available

  • UOC Dermatologia - Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

    Milano,
    Italy

    Site Not Available

  • UOC Clinica Dermatologica - AOU "Luigi Vanvitelli"

    Napoli,
    Italy

    Site Not Available

  • SCDU Dermatologia; AOU Maggiore della Carità di Novara

    Novara,
    Italy

    Site Not Available

  • SC Dermatologia - Fondazione IRCCS Policlinico San Matteo Clinica Dermatologica

    Pavia,
    Italy

    Site Not Available

  • UOSD Porfirie e Malattie rare - Istituto Dermatologico San Gallicano- IRCCS

    Roma,
    Italy

    Site Not Available

  • UO Dermatologia - IRCCS Humanitas

    Rozzano,
    Italy

    Site Not Available

  • SC Dermatologia U - AOU Città della Salute e della Scienza di Torino

    Torino,
    Italy

    Site Not Available

  • UOC Dermatologia e Venerologia - ASP Trapani, PO Sant'Antonio Abate

    Trapani,
    Italy

    Site Not Available

  • UOC Dermatologia - Azienda Ospedaliera Universitaria Integrata di Verona

    Verona,
    Italy

    Site Not Available

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