The detection of circulating plasma cells may improve the Revised International Staging System (R‐ISS) risk stratification of patients with newly diagnosed multiple myeloma

医学 危险分层 多发性骨髓瘤 内科学 生物标志物 阶段(地层学) 总体生存率 肿瘤科 胃肠病学 回顾性队列研究 生物 古生物学 生物化学
作者
Piero Galieni,Fosco Travaglini,Davide Vagnoni,Miriana Ruggieri,Patrizia Caraffa,Catia Bigazzi,Sadia Falcioni,Paola Picardi,Serena Mazzotta,Emanuela Troiani,Alessia Dalsass,Francesca Mestichelli,Mario Angelini,Elisa Camaioni,Denise Maravalle,Stefano Angelini,Valerio Pezzoni
出处
期刊:British Journal of Haematology [Wiley]
卷期号:193 (3): 542-550 被引量:24
标识
DOI:10.1111/bjh.17118
摘要

Summary The Revised International Staging System (R‐ISS) stratifies patients affected by Multiple Myeloma (MM) into three distinct risk groups: R‐ISS I [ISS Stage I, Standard‐Risk cytogenetics and normal Lactase DeHydrogenase (LDH)], R‐ISS III (ISS stage III and either high‐risk cytogenetics or high LDH) and R‐ISS II (any other characteristics). With the aim to verify whether the three R‐ISS groups could be divided into subgroups with different prognostic factors based on the detection of Circulating Plasma Cells (CPCs) at diagnosis, in this retrospective analysis, we evaluated 161 patients with MM treated at our centre between 2005 and 2017. In all, 57 patients (33·9%) were staged as R‐ISS III, 98 (58·3%) as R‐ISS II and six (3·6%) as R‐ISS I. CPCs were detected in 125 patients (74·4%), while in 43 patients (25·6%) no CPCs were seen. Our analysis revealed that Overall Survival (OS) and progression‐free survival (PFS) rates in R‐ISS II patients were higher in the subgroup without CPCs compared to the subgroup with ≥1 CPCs (OS: 44·7% vs. 16·3%, P = 0·0089; PFS: 27·8% vs. 8·1%, P = 0·0118). Our present findings suggest that the detection of CPCs at diagnosis may be used as a further prognostic biomarker to improve the risk stratification of patients with MM staged as R‐ISS II.
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