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Cutaneous Lymphoma International Consortium Study of Outcome in Advanced Stages of Mycosis Fungoides and Sézary Syndrome: Effect of Specific Prognostic Markers on Survival and Development of a Prognostic Model

蕈样真菌病 医学 内科学 皮肤T细胞淋巴瘤 国际预后指标 外周T细胞淋巴瘤 肿瘤科 胃肠病学 淋巴瘤 阶段(地层学) 免疫学 弥漫性大B细胞淋巴瘤 T细胞 免疫系统 生物 古生物学
作者
Julia Scarisbrick,H. Miles Prince,Maarten H. Vermeer,Pietro Quaglino,Sarah McCue Horwitz,Pierluigi Porcu,Rudolf Stadler,Gary S. Wood,M. Beylot‐Barry,Anne Pham‐Ledard,Francine M. Foss,Michael Girardi,M. Bagot,Laurence Michel,Maxime Battistella,Joan Guitart,Timothy M. Kuzel,Maria Estela Martínez‐Escala,Teresa Estrach,Evangelia Papadavid,Christina Antoniou,Dimitis Rigopoulos,Vassilki Nikolaou,Makoto Sugaya,Tomomitsu Miyagaki,Robert Gniadecki,José Antônio Sanches,Jade Cury‐Martins,Denis Miyashiro,Octavio Servitje,Cristina Muniesa,Emilio Berti,Francesco Onida,Laura Corti,Emilia Hodak,Iris Amitay‐Laish,Pablo L. Ortiz‐Romero,José Luis Rodríguez‐­Peralto,Robert Knobler,Stefanie Porkert,Wolfgang Bauer,Nicola Pimpinelli,Vieri Grandi,Richard Cowan,Alain H. Rook,Ellen Kim,Alessandro Pileri,Annalisa Patrizi,Ramón M. Pujol,Henry K. Wong,Kelly Tyler,R. Stranzenbach,Christiane Querfeld,Paolo Fava,Milena Maule,Rein Willemze,Felicity Evison,Stephen Morris,Robert Twigger,Rakhshandra Talpur,Jinah Kim,G. Ognibene,Shufeng Li,Mahkam Tavallaee,Richard T. Hoppe,Madeleine Duvic,Sean Whittaker,Youn H. Kim
出处
期刊:Journal of Clinical Oncology [Lippincott Williams & Wilkins]
卷期号:33 (32): 3766-3773 被引量:344
标识
DOI:10.1200/jco.2015.61.7142
摘要

Purpose Advanced-stage mycosis fungoides (MF; stage IIB to IV) and Sézary syndrome (SS) are aggressive lymphomas with a median survival of 1 to 5 years. Clinical management is stage based; however, there is wide range of outcome within stages. Published prognostic studies in MF/SS have been single-center trials. Because of the rarity of MF/SS, only a large collaboration would power a study to identify independent prognostic markers. Patients and Methods Literature review identified the following 10 candidate markers: stage, age, sex, cutaneous histologic features of folliculotropism, CD30 positivity, proliferation index, large-cell transformation, WBC/lymphocyte count, serum lactate dehydrogenase, and identical T-cell clone in blood and skin. Data were collected at specialist centers on patients diagnosed with advanced-stage MF/SS from 2007. Each parameter recorded at diagnosis was tested against overall survival (OS). Results Staging data on 1,275 patients with advanced MF/SS from 29 international sites were included for survival analysis. The median OS was 63 months, with 2- and 5-year survival rates of 77% and 52%, respectively. The median OS for patients with stage IIB disease was 68 months, but patients diagnosed with stage III disease had slightly improved survival compared with patients with stage IIB, although patients diagnosed with stage IV disease had significantly worse survival (48 months for stage IVA and 33 months for stage IVB). Of the 10 variables tested, four (stage IV, age > 60 years, large-cell transformation, and increased lactate dehydrogenase) were independent prognostic markers for a worse survival. Combining these four factors in a prognostic index model identified the following three risk groups across stages with significantly different 5-year survival rates: low risk (68%), intermediate risk (44%), and high risk (28%). Conclusion To our knowledge, this study includes the largest cohort of patients with advanced-stage MF/SS and identifies markers with independent prognostic value, which, used together in a prognostic index, may be useful to stratify advanced-stage patients.
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