A new prognostic index (CLIPI) for advanced cutaneous lymphoma enables precise patient risk stratification

蕈样真菌病 国际预后指标 医学 胃肠病学 阶段(地层学) 淋巴瘤 皮肤T细胞淋巴瘤 内科学 前瞻性队列研究 肿瘤科 外科 弥漫性大B细胞淋巴瘤 生物 古生物学
作者
Julia Scarisbrick,Pietro Quaglino,Sean Whittaker,M. Bagot,Emmanuella Guenova,Evangelia Papadavid,H. Miles Prince,José Antônio Sanches,Denis Miyashiro,Octavio Servitje,Christiane Querfeld,Oleg E. Akilov,Arvind Arumainathan,Luke Bennett,Maxime Battistella,Kim Benstead,Emilio Berti,M. Beylot‐Barry,Anne-Marie Busschots,Richard Cowan
出处
期刊:Blood [Elsevier BV]
卷期号:146 (14): 1687-1692 被引量:13
标识
DOI:10.1182/blood.2025029628
摘要

Advanced mycosis fungoides (MF) and Sézary syndrome (SS) have a poor overall survival (OS) of <5 years. Studies have found the current staging (IA-IVB) is inadequate for risk stratification. The PROCLIPI (Prospective Cutaneous Lymphoma International Prognostic Index) study was launched in 2015 at 46 international expert MF/SS centers, prospectively collecting predefined data sets in patients with newly diagnosed MF/SS, to determine a cutaneous lymphoma IPI (CLIPI). Five hundred fifty-two patients with advanced stage MF/SS were recruited. The 5-year OS was 50.0% for stage IIB, 64.8% for stage IIIA, 43.9% for stage IIIB, 50.8% for stage IVA1, 25.9% for stage IVA2, and 36.9% for stage IVB. Factors at diagnosis associated with a significantly worse survival were N3 status (P < .001), age >60 years (P < .001), raised serum lactate dehydrogenase (P = .005), and large-cell transformation in skin (P = .006). Modeling these 4 independent risk factors into a CLIPI found that there was a worse OS in high- vs low-risk (P < .001), high- vs intermediate-risk (P = .002) and intermediate- vs low-risk (P = .010) groups. Five-year OS was 63.3%, 44.7%, and 18.3% in the low-, intermediate-, and high-risk groups, respectively. In this advanced stage cohort there was a low 5-year survival and increasing stage was not associated with worsening survival. The use of CLIPI to stratify patients into risk groups has the potential to improve outcomes and aid optimal treatment selection. This trial was registered at www.ClinicalTrials.gov as #NCT02848274.
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