Subcutaneous panniculitis-like T-cell lymphoma: definition, classification, and prognostic factors: an EORTC Cutaneous Lymphoma Group Study of 83 cases

Rein Willemze, Patty M. Jansen(Leiden University Medical Center), Lorenzo Cerroni(University of Graz), Emilio Berti(University of Milan), Marco Santucci(University of Florence), Chalid Assaf(Charité - Universitätsmedizin Berlin), Marijke R. Canninga‐van Dijk(University Medical Center Utrecht), A. Carlotti(Université Paris Cité), Marie‐Louise Geerts(Ghent University Hospital), Sonja Hahtola(Helsinki University Hospital), Michael Hummel(Charité - Universitätsmedizin Berlin), Leila Jeskanen(Helsinki University Hospital), Werner Kempf(University Hospital of Zurich), Cesare Massone(University of Graz), Pablo L. Ortiz‐Romero(Hospital Universitario 12 De Octubre), Marco Paulli(University of Pavia), Tony Petrella(Maison des Sciences sociales et des Humanités de Dijon), Annamari Ranki(Helsinki University Hospital), José Luis Rodríguez‐­Peralto(Hospital Universitario 12 De Octubre), Alistair Robson(St Thomas' Hospital), Nancy J. Senff, Maarten H. Vermeer, Janine Wechsler, Sean Whittaker(St Thomas' Hospital), Chris J.L.M. Meijer(Vrije Universiteit Amsterdam)
Blood
October 13, 2007
Cited by 695

Abstract

In the WHO classification, subcutaneous panniculitis-like T-cell lymphoma (SPTL) is defined as a distinct type of T-cell lymphoma with an aggressive clinical behavior. Recent studies suggest that distinction should be made between SPTL with an alpha/beta T-cell phenotype (SPTL-AB) and SPTL with a gammadelta T-cell phenotype (SPTL-GD), but studies are limited. To better define their clinicopathologic features, immunophenotype, treatment, and survival, 63 SPTL-ABs and 20 SPTL-GDs were studied at a workshop of the EORTC Cutaneous Lymphoma Group. SPTL-ABs were generally confined to the subcutis, had a CD4-, CD8+, CD56-, betaF1+ phenotype, were uncommonly associated with a hemophagocytic syndrome (HPS; 17%), and had a favorable prognosis (5-year overall survival [OS]: 82%). SPTL-AB patients without HPS had a significantly better survival than patients with HPS (5-year OS: 91% vs 46%; P<.001). SPTL-GDs often showed (epi)dermal involvement and/or ulceration, a CD4-, CD8-, CD56+/-, betaF1- T-cell phenotype, and poor prognosis (5-year OS: 11%), irrespective of the presence of HPS or type of treatment. These results indicate that SPTL-AB and SPTL-GD are distinct entities, and justify that the term SPTL should further be used only for SPTL-AB. SPTL-ABs without associated HPS have an excellent prognosis, and multiagent chemotherapy as first choice of treatment should be questioned.


Related Papers

No related papers found

Powered by citation graph analysis