Predictors for the use of systemic therapy in stage IB Mycosis fungoides.


Journal

Archives of dermatological research
ISSN: 1432-069X
Titre abrégé: Arch Dermatol Res
Pays: Germany
ID NLM: 8000462

Informations de publication

Date de publication:
06 Jun 2024
Historique:
received: 12 04 2024
accepted: 26 04 2024
revised: 12 04 2024
medline: 7 6 2024
pubmed: 7 6 2024
entrez: 6 6 2024
Statut: epublish

Résumé

The PROspective Cutaneous Lymphoma International Prognostic Index (PROCLIPI) study is aprospective analysis of an international database. Here we examine front-line treatments and quality of life (QoL) inpatients with newly diagnosed mycosis fungoides (MF). To identify (i) differences in first-line approaches according to tumour-nodes-metastasis-blood (TNMB)staging; (ii) parameters related to a first-line systemic approach and (iii) response rates and QoL measures. In total, 395 newly diagnosed patients with early-stage MF (stage IA-IIA) were recruited from 41 centresin 17 countries between 1 January 2015 and 31 December 2018 following central clinicopathological review. The most common first-line therapy was skin-directed therapy (SDT) (322 cases, 81·5%), while a smallerpercentage (44 cases, 11·1%) received systemic therapy. Expectant observation was used in 7·3%. In univariateanalysis, the use of systemic therapy was significantly associated with higher clinical stage (IA, 6%; IB, 14%; IIA,20%; IA-IB vs. IIA, P < 0·001), presence of plaques (T1a/T2a, 5%; T1b/T2b, 17%; P < 0·001), higher modified Severity Weighted Assessment Tool (> 10, 15%; ≤ 10, 7%; P = 0·01) and folliculotropic MF (FMF) (24% vs. 12%, P = 0·001). Multivariate analysis demonstrated significant associations with the presence of plaques (T1b/T2b vs.T1a/T2a, odds ratio 3·07) and FMF (odds ratio 2·83). The overall response rate (ORR) to first-line SDT was 73%,while the ORR to first-line systemic treatments was lower (57%) (P = 0·027). Health-related QoL improvedsignificantly both in patients with responsive disease and in those with stable disease. Disease characteristics such as presence of plaques and FMF influence physician treatment choices,and SDT was superior to systemic therapy even in patients with such disease characteristics. Consequently, futuretreatment guidelines for early-stage MF need to address these issues.

Sections du résumé

BACKGROUND BACKGROUND
The PROspective Cutaneous Lymphoma International Prognostic Index (PROCLIPI) study is aprospective analysis of an international database. Here we examine front-line treatments and quality of life (QoL) inpatients with newly diagnosed mycosis fungoides (MF).
OBJECTIVES OBJECTIVE
To identify (i) differences in first-line approaches according to tumour-nodes-metastasis-blood (TNMB)staging; (ii) parameters related to a first-line systemic approach and (iii) response rates and QoL measures.
METHODS METHODS
In total, 395 newly diagnosed patients with early-stage MF (stage IA-IIA) were recruited from 41 centresin 17 countries between 1 January 2015 and 31 December 2018 following central clinicopathological review.
RESULTS RESULTS
The most common first-line therapy was skin-directed therapy (SDT) (322 cases, 81·5%), while a smallerpercentage (44 cases, 11·1%) received systemic therapy. Expectant observation was used in 7·3%. In univariateanalysis, the use of systemic therapy was significantly associated with higher clinical stage (IA, 6%; IB, 14%; IIA,20%; IA-IB vs. IIA, P < 0·001), presence of plaques (T1a/T2a, 5%; T1b/T2b, 17%; P < 0·001), higher modified Severity Weighted Assessment Tool (> 10, 15%; ≤ 10, 7%; P = 0·01) and folliculotropic MF (FMF) (24% vs. 12%, P = 0·001). Multivariate analysis demonstrated significant associations with the presence of plaques (T1b/T2b vs.T1a/T2a, odds ratio 3·07) and FMF (odds ratio 2·83). The overall response rate (ORR) to first-line SDT was 73%,while the ORR to first-line systemic treatments was lower (57%) (P = 0·027). Health-related QoL improvedsignificantly both in patients with responsive disease and in those with stable disease.
CONCLUSIONS CONCLUSIONS
Disease characteristics such as presence of plaques and FMF influence physician treatment choices,and SDT was superior to systemic therapy even in patients with such disease characteristics. Consequently, futuretreatment guidelines for early-stage MF need to address these issues.

Identifiants

pubmed: 38844623
doi: 10.1007/s00403-024-03005-0
pii: 10.1007/s00403-024-03005-0
doi:

Types de publication

Journal Article Multicenter Study Letter

Langues

eng

Sous-ensembles de citation

IM

Pagination

337

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

Galper SL, Smith BD, Wilson LD (2010) Diagnosis and management of mycosis fungoides. Oncol (Williston Park) 24(6):491–501
Cerroni L (2018) Mycosis fungoides-clinical and histopathologic features, differential diagnosis, and treatment. Semin Cutan Med Surg 37(1):2–10
doi: 10.12788/j.sder.2018.002 pubmed: 29719014
Quaglino P et al (2021) Treatment of early-stage mycosis fungoides: results from the PROspective cutaneous Lymphoma International Prognostic Index (PROCLIPI) study. Br J Dermatol 184(4):722–730
doi: 10.1111/bjd.19252 pubmed: 32479678 pmcid: 7704558
Trautinger F et al (2017) European Organisation for Research and Treatment of Cancer consensus recommendations for the treatment of mycosis fungoides/Sézary syndrome - update 2017. Eur J Cancer 77:57–74
doi: 10.1016/j.ejca.2017.02.027 pubmed: 28365528
Bahalı AG et al (2020) Prognostic factors of patients with mycosis fungoides. Postepy Dermatol Alergol 37(5):796–799
doi: 10.5114/ada.2020.100491 pubmed: 33240023 pmcid: 7675080

Auteurs

Elijah Rodriguez (E)

The Ronald O. Perelman Department of Dermatology, New York University Grossman School of Medicine, 240 East 38th Street, Floor 11, New York, NY, 10016, USA.

Carli D Needle (CD)

The Ronald O. Perelman Department of Dermatology, New York University Grossman School of Medicine, 240 East 38th Street, Floor 11, New York, NY, 10016, USA.

Michael J Martinez (MJ)

The Ronald O. Perelman Department of Dermatology, New York University Grossman School of Medicine, 240 East 38th Street, Floor 11, New York, NY, 10016, USA.

Ambika Nohria (A)

The Ronald O. Perelman Department of Dermatology, New York University Grossman School of Medicine, 240 East 38th Street, Floor 11, New York, NY, 10016, USA.

Yiping Xing (Y)

Hackensack University Medical Center, Hackensack, NJ, USA.

Clara Song (C)

Department of Biostatistics, New York University School of Global Public Health, New York, NY, USA.

Rebecca Betensky (R)

Department of Biostatistics, New York University School of Global Public Health, New York, NY, USA.

Jo-Ann Latkowski (JA)

The Ronald O. Perelman Department of Dermatology, New York University Grossman School of Medicine, 240 East 38th Street, Floor 11, New York, NY, 10016, USA.

Prince Adotama (P)

The Ronald O. Perelman Department of Dermatology, New York University Grossman School of Medicine, 240 East 38th Street, Floor 11, New York, NY, 10016, USA. prince.adotama@nyulangone.org.

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