Cutaneous Lymphoma

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Molecular Cancer Biology".

Deadline for manuscript submissions: 1 December 2024 | Viewed by 1931

Special Issue Editor


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Guest Editor
Department of Dermatology, University of Washington, Seattle, WA 98195, USA
Interests: cutaneous lymphoma; cutaneous T-cell lymphoma; mycosis fungoides; quality of life

Special Issue Information

Dear Colleagues,

Primary cutaneous lymphomas (PCLs) are a heterogeneous group of non-Hodgkin lymphomas and include the more common primary cutaneous T-cell lymphomas (CTCLs) as well as primary cutaneous B-cell lymphomas (CBCLs). Despite their unifying T-cell origin, the most common CTCL subtypes (mycosis fungoides, Sézary syndrome, and CD30 lymphoproliferative disorders) exhibit a wide variety of clinical and histologic characteristics.

For this Special Issue, we invite authors to submit high-quality original research and review articles that advance our understanding of PCL. Topics may include (but are not limited to) the pathophysiology of disease, molecular and biological markers for cutaneous lymphoma, novel therapies, and supportive care and quality of life.

Dr. Michi M. Shinohara
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Cancers is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2900 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • primary cutaneous lymphoma
  • cutaneous T-cell lymphoma
  • mycosis fungoides
  • Sézary syndrome
  • health-related quality of life

Published Papers (2 papers)

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Research

10 pages, 234 KiB  
Article
Evaluation of Quality of Life and Treatment Satisfaction in Newly Diagnosed Cutaneous T-Cell Lymphoma Patients
by Rosanne Ottevanger, Sylvia van Beugen, Juliette M. Kersten, Andrea W. M. Evers, Maarten H. Vermeer, Rein Willemze and Koen D. Quint
Cancers 2024, 16(5), 937; https://doi.org/10.3390/cancers16050937 - 26 Feb 2024
Viewed by 661
Abstract
Background: Little is known about the impact of MF on quality of life (QoL) in newly diagnosed patients. Objectives: To describe the impact of the MF diagnosis on QoL, patient expectations, and treatment satisfaction over the first 6 months after diagnosis. Methods: Outcomes [...] Read more.
Background: Little is known about the impact of MF on quality of life (QoL) in newly diagnosed patients. Objectives: To describe the impact of the MF diagnosis on QoL, patient expectations, and treatment satisfaction over the first 6 months after diagnosis. Methods: Outcomes of this prospective cohort study of newly diagnosed MF patients conducted between 2020 and 2022 at the Leiden University Medical Center included the Skindex-29, RAND-12 Health Survey, degree of itch, pain, and fatigue (Visual Analogue Scale (VAS)), patient expectations, and Client Satisfaction Questionnaire-8 (CSQ-8), measured at baseline and after six months. Results: A total of 28 patients with MF were included. At baseline, 66% (n = 18) “strongly-totally” expected positive effects of the treatment. At the time of diagnosis, 28% of the patients (n = 8) were moderately to severely affected. There was no statistical change in the Skindex-29 score sum score (20 [10–34] vs. 20 [9–36]; p = 0.81) or in the other three subdomains, the RAND-12 scores, and the VAS itch, pain, and fatigue over time. Treatment satisfaction was high overall. Conclusion: Despite that the newly diagnosed MF patients anticipate a positive treatment effect, few improvements in QoL and symptom reduction were found. These data can be used for adequate expectation management and provide a rationale for further evaluation of treatment regimens in these patients. Full article
(This article belongs to the Special Issue Cutaneous Lymphoma)
14 pages, 997 KiB  
Article
A Retrospective Chart Review of Treatment Patterns and Overall Survival among a Cohort of Patients with Relapsed/Refractory Mycosis Fungoides in France, Germany, Italy, Spain and the United Kingdom
by Chalid Assaf, Timothy M. Illidge, Nathalie Waser, Mary He, Tina Li, Athanasios Zomas, Nawal Bent-Ennakhil, Meredith Little, Pablo L. Ortiz-Romero, Nicola Pimpinelli, Mehul Dalal and Martine Bagot
Cancers 2023, 15(23), 5669; https://doi.org/10.3390/cancers15235669 - 30 Nov 2023
Viewed by 1021
Abstract
(1) Background: Most patients with mycosis fungoides (MF), a form of cutaneous T-cell lymphoma (CTCL), develop relapsed/refractory (R/R) disease following front-line systemic therapy. This report describes treatment patterns and outcomes from the subpopulation with R/R MF. (2) Methods: This observational, retrospective, cohort study [...] Read more.
(1) Background: Most patients with mycosis fungoides (MF), a form of cutaneous T-cell lymphoma (CTCL), develop relapsed/refractory (R/R) disease following front-line systemic therapy. This report describes treatment patterns and outcomes from the subpopulation with R/R MF. (2) Methods: This observational, retrospective, cohort study analyzed patient records (1984–2016) from 27 clinical sites in Europe. Outcomes included treatments received, response to first-, second- and third-line treatment, overall survival (OS) and progression-free survival (PFS). (3) Results: Of 104 patients with MF, 100 received second-line and 61 received third-line therapy. The median (range) times from the start of first-line therapy to the first R/R MF and from the first to the second R/R MF were 11.2 (0.3–166.5) and 13.5 (0.0–174.6) months, respectively. Second-and third-line treatment options varied and comprised systemic therapies (85% and 79% of patients, respectively), radiotherapy (32% and 34%, respectively) and topical therapies (48% and 36%, respectively). The median (95% confidence interval [CI]) OS from the diagnosis of the first R/R MF was 11.5 (6.5–not reached [NR]) years and was higher with non-chemotherapy (NR) versus chemotherapy (6.5 years); the estimated median PFS (95% CI) from the time of the first R/R MF was 1.3 (1.0–2.1) years. (4) Conclusions: High rates of R/R disease were observed after second- and third-line treatments in this real-world cohort, with longer median OS in patients receiving non-chemotherapy treatment versus chemotherapy. Following the standard management of MF and using recently approved targeted therapies can help improve patient outcomes in advanced-stage MF. Full article
(This article belongs to the Special Issue Cutaneous Lymphoma)
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