Circulating Multiple Myeloma Cells (CMMCs) as Prognostic and Predictive Markers in Multiple Myeloma and Smouldering MM Patients

Author:

Vigliotta Ilaria1ORCID,Solli Vincenza2ORCID,Armuzzi Silvia2ORCID,Martello Marina2ORCID,Poletti Andrea2ORCID,Taurisano Barbara2,Pistis Ignazia1,Mazzocchetti Gaia2ORCID,Borsi Enrica1ORCID,Pantani Lucia1,Marzocchi Giulia2,Testoni Nicoletta12,Zamagni Elena12ORCID,Terracciano Mario3,Tononi Paola3,Garonzi Marianna3,Ferrarini Alberto3ORCID,Manaresi Nicolò3ORCID,Cavo Michele12ORCID,Terragna Carolina1

Affiliation:

1. IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia “Seràgnoli”, 40138 Bologna, Italy

2. Department of Medical and Surgical Sciences, University of Bologna, 40126 Bologna, Italy

3. Menarini Silicon Biosystems SpA, Via Giuseppe di Vittorio, Castel Maggiore, 40013 Bologna, Italy

Abstract

In recent years, liquid biopsy has emerged as a promising alternative to the bone marrow (BM) examination, since it is a minimally invasive technique allowing serial monitoring. Circulating multiple myeloma cells (CMMCs) enumerated using CELLSEARCH® were correlated with patients’ prognosis and measured under treatment to assess their role in monitoring disease dynamics. Forty-four MM and seven smouldering MM (SMM) patients were studied. The CMMC medians at diagnosis were 349 (1 to 39,940) and 327 (range 22–2463) for MM and SMM, respectively. In the MM patients, the CMMC count was correlated with serum albumin, calcium, β2-microglobulin, and monoclonal components (p < 0.04). Under therapy, the CMMCs were consistently detectable in 15/40 patients (coMMstant = 1) and were undetectable or decreasing in 25/40 patients (coMMstant = 0). High-quality response rates were lower in the coMMstant = 1 group (p = 0.04), with a 7.8-fold higher risk of death (p = 0.039), suggesting that continuous CMMC release is correlated with poor responses. In four MM patients, a single-cell DNA sequencing analysis on residual CMMCs confirmed the genomic pattern of the aberrations observed in the BM samples, also highlighting the presence of emerging clones. The CMMC kinetics during treatment were used to separate the patients into two subgroups based on the coMMstant index, with different responses and survival probabilities, providing evidence that CMMC persistence is associated with a poor disease course.

Funder

Italian Ministry of Health

Publisher

MDPI AG

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