“Since there is no consensus on how to stratify patients with MM based on CTCs, we performed an analysis among 2,466 patients with newly diagnosed MM to investigate this matter,” said Dr Luca Bertamini (University of Turin, Italy) [1]. The study comprised a diverse population: 45% of the patients were 65 years or older, 48% were ineligible for transplant, and 59% participated in clinical trials.
After a median follow-up of 56.8 months, the median CTC level was 0.017%, with no observed differences between the datasets from the 6 participating European countries. Dr Bertamini highlighted that continuous CTC levels were prognostic of PFS outcomes. “We were able to discriminate between 5 groups of patients with different CTC levels in terms of PFS,” he said. “Patients with high CTC levels had a significantly shorter PFS duration than those with low CTC levels [P<0.0001]. Moreover, CTC level was an independent predictor for PFS [HR 1.18; 95% CI 1.12-1.24; P<0.001].” The research team determined the optimal CTC cut-off level for clinical use at 0.02%. “Patients with CTC levels of 0.02% or lower outperformed patients with CTC levels above 0.02% in terms of PFS,” clarified Dr Bertamini. CTC levels were prognostic for PFS across clinical trial and real-world subgroups, as well as for transplant-eligible and transplant-ineligible patients.
Thus, CTC may serve as an independent prognostic factor for survival outcomes in patients with MM, finetuning the risk assessment for the population, concluded Dr Bertamini. Incorporating CTC levels into standard risk stratification may improve the prognostic ability of these classification tools.
- Bertamini L, et al. Circulating tumour cells for the staging of multiple myeloma: a European pooled analysis of 2,446 newly diagnosed patients. S199, EHA2025 Congress, 12–15 June, Milan, Italy.
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Table of Contents: EHA 2025
Featured articles
Letter from the Editor
Non-Malignant Haematology
Promising safety and efficacy data for novel anti-CD38 treatment in ITP
Novel investigational gene-editing therapy for TDT and SCD
HSCT may reduce risk of ocular complications in SCD
Are PBSCs a viable source for haplo-HSCT in SCD?
Multiple Myeloma/Plasma Cell Disorders
Large pooled analysis reveals prognostic utility of circulating tumour cells in MM
RedirecTT-1: Dual antigen-targeting treatment associated with promising efficacy in EMD myeloma
Prognostic impact of circulating tumour cells in AL amyloidosis
IRAKLIA: Novel isatuximab delivery system improves patient satisfaction in MM
MagnetisMM-6: Excellent early results of elranatamab in MM
MIDAS: Is ASCT needed in MM after reaching MRD-negativity with IsaKRD?
Novel trispecific antibody may be a game-changer for relapsed/refractory MMF
Lymphoma
GAIA/CLL13: Positive 5-year efficacy outcomes for GIV in CLL
ELM-2: Survival benefit for patients with FL on odronextamab
inMIND: Positive phase 3 results for tafasitamab combination in FL
Unravelling real-world safety and effectiveness of axi-cel in LBCL
STARGLO: Long-term clinical benefits of Glofit-GemOx over R-GemOx in DLBCL
ECHO: Older patients with high-risk MCL benefit from acalabrutinib added to BR
POLARGO: Pola-R-GemOx delivers overall survival benefit in second-line DLBCL
Acute Leukaemia (AML and ALL)
Refined AML risk prediction by improved understanding of genetics
TUSCANY: Promising data for the addition of tuspetinib in untreated chemo-ineligible AML
Chemogenomic profiling appears reliable strategy to improve outcomes in T-ALL/ETP-ALL
Dasatinib does not cross the finish line in the phase 3 AML study
Myeloid Neoplasms
ASC4START: asciminib showed superior tolerability to nilotinib in CML
Encouraging results for new mutation-specific targeted therapy in CALR-mutated ET
Improving diagnosis, classification, and prognosis of MDN with an AI-based model
SURPASS-ET: Ropeg meets primary endpoint in essential thrombocythemia
MANIFEST-2: Sustained benefits of pelabresib plus ruxolitinib in myelofibrosis
Stem Cell Transplantation
Targeted anti-thymocyte globulin dosing improves transplantation outcomes
HCT Frailty Scale may refine the allo-HCT selection process
Ravulizumab shows tolerability and efficacy in HSCT-thrombotic microangiopathy
ALLG BM12 CAST: improved GRFS through novel GVHD prophylaxis
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