Rüfer Axel, Nilius Henning, Hermine Olivier, Niedoszytko Marek, Oude Elberink Joanne N G, Bonadonna Patrizia, Shoumariyeh Khalid, Gulen Theo, Hartmann Karin, Sabato Vito, Angelova-Fischer Irena, Baffoe Daniel, Christen Deborah, Belloni Fortina Anna, Breynaert Christine, Brockow Knut, von Bubnoff Nikolas, Bumbea Horia, van Daele Paul, Doubek Michael, Dybedal Ingunn, Elena Chiara, Fokoloros Christos, Górska Aleksandra, Heizmann Marc, Jentzsch Madlen, Klein Saskia, Lübke Johannes, Mattsson Mattias, Mulder André, Panse Jens, Schug Tanja Daniela, Sciumè Mariarita, Stefan Alex, Sztormowska Marlena, Várkonyi Judit, Wortmann Friederike, Yavuz Akif Selim, Sperr Martina, Gotlib Jason, Reiter Andreas, Triggiani Massimo, Sperr Wolfgang R, Valent Peter
Department of Hematology, Luzerner Kantonsspital, University of Luzern, Luzern, Switzerland.
Department of Clinical Chemistry, University Hospital Bern, Inselspital, Bern, Switzerland.
Leukemia. 2025 Mar;39(3):675-683. doi: 10.1038/s41375-024-02504-3. Epub 2025 Jan 15.
Expression of CD2, CD25 and/or CD30 in extracutaneous mast cells (MC) is a minor diagnostic criterion for systemic mastocytosis (SM) in the classification of the World Health Organization and International Consensus Classification. So far, it remains unknown whether expression of these antigens on MC is of prognostic significance in SM. We performed a retrospective multi-center study of patients with SM using the data set of the registry of the European Competence Network on Mastocytosis, including 5034 patients with various MC disorders. The percentage of CD2, CD25 and/or CD30 MC was considerably lower in patients with indolent SM compared to patients with advanced SM, including aggressive SM and MC leukemia. Whereas CD25 and CD30 expression in MC could not be associated with prognosis, we found that lack of CD2 expression in MC is associated with a significantly reduced overall survival (OS) in patients with SM (p < 0.0001). Lack of CD2 was also associated with the presence of extramedullary involvement affecting the spleen, liver, and/or lymph nodes (odds ratio 2.63 compared to SM with CD2 MC). Together, lack of CD2 expression in MC is a prognostic marker and indicator of reduced OS and extramedullary disease expansion in patients with SM.
在世界卫生组织和国际共识分类中,皮肤外肥大细胞(MC)中CD2、CD25和/或CD30的表达是系统性肥大细胞增多症(SM)的次要诊断标准。迄今为止,尚不清楚这些抗原在MC上的表达在SM中是否具有预后意义。我们利用欧洲肥大细胞增多症能力网络登记处的数据集对SM患者进行了一项回顾性多中心研究,包括5034例患有各种MC疾病的患者。与晚期SM患者(包括侵袭性SM和MC白血病)相比,惰性SM患者中CD2、CD25和/或CD30 MC的百分比要低得多。虽然MC中CD25和CD30的表达与预后无关,但我们发现MC中缺乏CD2表达与SM患者的总生存期(OS)显著降低相关(p<0.0001)。缺乏CD2还与影响脾脏、肝脏和/或淋巴结的髓外受累有关(与具有CD2 MC的SM相比,优势比为2.63)。总之,MC中缺乏CD2表达是SM患者OS降低和髓外疾病扩展的预后标志物和指标。