Literature DB >> 29477101

Blood classification and blood response criteria in mycosis fungoides and Sézary syndrome using flow cytometry: recommendations from the EORTC cutaneous lymphoma task force.

Julia J Scarisbrick1, Emmilia Hodak2, Martine Bagot3, Rene Stranzenbach4, Rudolf Stadler4, Pablo L Ortiz-Romero5, Evangelia Papadavid6, Felicity Evison7, Robert Knobler8, Pietro Quaglino9, Maarten H Vermeer10.   

Abstract

Our current mycosis fungoides (MF) and Sézary Syndrome (SS) staging system includes blood-classification from B0-B2 for patch/plaque/tumour or erythroderma based on manual Sézary counts but results from our EORTC survey confirm these are rarely performed in patch/plaque/tumour MF, and there is a trend towards using flow cytometry to measure blood-class. Accurately assigning blood-class effects overall stage and the 'global response' used to measure treatment responses in MF/SS and hence impacts management. The EORTC Cutaneous Lymphoma Task Force Committee have reviewed the literature and held a Workshop (June 2017) to agree a definition of blood-class according to flow cytometry. No large study comparing blood-class as defined by Sézary count with flow cytometry has been performed in MF/SS. The definition of blood-class by flow cytometry varies between publications. Low-level blood involvement occurs in patch/plaque/tumour much less than erythroderma (p < 0.001). The prognostic relevance of blood involvement (B1 or B2) in patch/plaque/tumour is not known. Studies have not shown a statistically worse difference in prognosis in erythrodermic MF patients with low-level blood involvement (IIIB) versus those without (IIIA), but Sezary patients who by definition have a leukaemic blood picture (staged IVA1 or higher) have a worse prognosis. For consistency flow, definition for blood-class must be an objective measurement. We propose absolute counts of either CD4+CD7-or CD4+CD26-where B0<250/μL, B1 = 250/μl-<1000/μL and B2≥1000/μL plus a T-cell blood clone. Fluctuations between B0 and B1 should not be considered in the treatment response criteria until further prognostic information is known.
Copyright © 2018 The Authors. Published by Elsevier Ltd.. All rights reserved.

Entities:  

Keywords:  Blood; CD26; CD7; Classification; Cutaneous T-cell lymphoma; Erythroderma; Staging

Mesh:

Year:  2018        PMID: 29477101     DOI: 10.1016/j.ejca.2018.01.076

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  25 in total

1.  Scleromyxedematous Changes in a Patient With Long-Standing Mycosis Fungoides Who Progressed to Sézary Syndrome.

Authors:  Allen P Miraflor; Melissa P Pulitzer; Patricia L Myskowski; Shamir Geller
Journal:  Am J Dermatopathol       Date:  2019-11       Impact factor: 1.533

Review 2.  Cutaneous T cell lymphoma.

Authors:  Reinhard Dummer; Maarten H Vermeer; Julia J Scarisbrick; Youn H Kim; Connor Stonesifer; Cornelis P Tensen; Larisa J Geskin; Pietro Quaglino; Egle Ramelyte
Journal:  Nat Rev Dis Primers       Date:  2021-08-26       Impact factor: 52.329

3.  Clinical characteristics and prognostic factors of 70 patients with Sézary syndrome: a single-institutional experience at Moffitt cancer center.

Authors:  Yumeng Zhang; Lucia Seminario-Vidal; Christa Varnadoe; Yuanyuan Lu; Ning Dong; Christopher Salamanca; Shannen Whiddon; Janice Bennett; Rebecca Hargis; Hien Liu; Michael Montejo; Mohammad Hussaini; Carly Harro; Jane Messina; Kaaron Benson; Javier Pinilla-Ibarz; Jose Conejo-Garcia; Lubomir Sokol
Journal:  Leuk Lymphoma       Date:  2021-09-01

4.  Mycosis fungoides and Sézary syndrome.

Authors:  Constanze Jonak; Julia Tittes; Patrick Manfred Brunner; Emmanuella Guenova
Journal:  J Dtsch Dermatol Ges       Date:  2021-09       Impact factor: 5.231

5.  Erythroderma: a prospective study of 309 patients followed for 12 years in a tertiary center.

Authors:  Denis Miyashiro; José Antonio Sanches
Journal:  Sci Rep       Date:  2020-06-17       Impact factor: 4.379

6.  ICOS is widely expressed in cutaneous T-cell lymphoma, and its targeting promotes potent killing of malignant cells.

Authors:  Florent Amatore; Nicolas Ortonne; Marc Lopez; Florence Orlanducci; Rémy Castellano; Saskia Ingen-Housz-Oro; Amandine De Croos; Clémentine Salvado; Laurent Gorvel; Armelle Goubard; Yves Collette; Réda Bouabdallah; Jean-Marc Schiano; Nathalie Bonnet; Jean-Jacques Grob; Philippe Gaulard; Martine Bagot; Armand Bensussan; Philippe Berbis; Daniel Olive
Journal:  Blood Adv       Date:  2020-10-27

7.  Xenograft and cell culture models of Sézary syndrome reveal cell of origin diversity and subclonal heterogeneity.

Authors:  Martina Prochazkova-Carlotti; Floriane Cherrier; Audrey Gros; Sandrine Poglio; Elodie Laharanne; Anne Pham-Ledard; Marie Beylot-Barry; Jean-Philippe Merlio
Journal:  Leukemia       Date:  2020-10-26       Impact factor: 11.528

8.  Cutaneous T-cell lymphomas: 2021 update on diagnosis, risk-stratification, and management.

Authors:  Alexandra C Hristov; Trilokraj Tejasvi; Ryan A Wilcox
Journal:  Am J Hematol       Date:  2021-08-02       Impact factor: 13.265

Review 9.  Sézary syndrome and mycosis fungoides: An overview, including the role of immunophenotyping.

Authors:  Melissa P Pulitzer; Pedro Horna; Julia Almeida
Journal:  Cytometry B Clin Cytom       Date:  2020-06-09       Impact factor: 3.248

10.  Blockade of programmed cell death protein 1 (PD-1) in Sézary syndrome reduces Th2 phenotype of non-tumoral T lymphocytes but may enhance tumor proliferation.

Authors:  Ieva Saulite; Desislava Ignatova; Yun-Tsan Chang; Christina Fassnacht; Florentia Dimitriou; Eleni Varypataki; Florian Anzengruber; Mirjam Nägeli; Antonio Cozzio; Reinhard Dummer; Julia Scarisbrick; Steve Pascolo; Wolfram Hoetzenecker; Malgorzata Bobrowicz; Emmanuella Guenova
Journal:  Oncoimmunology       Date:  2020-03-18       Impact factor: 8.110

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