“Although allogeneic HCT is a potentially curative option for patients with haematologic tumours, it comes with a substantial morbidity, mortality, and quality-of-life burden,” said Dr Maria Queralt Salas (Hospital Clinic de Barcelona, Spain). Her research group wondered whether the pre-transplant assessment should be refined. Traditionally, the eligibility for transplant is based on age and comorbidities. Dr Salas and colleagues designed a frailty scale and tested its prognostic value for overall survival (OS) and non-relapse mortality in adult patients who were candidates for allogeneic HCT (n=1,077) [1]. The HCT-FS includes measures such as the Clinical Frailty Scale, Timed Up and Go test, grip strength, serum albumin level, and falls in the last 6 months.
After the assessment, patients could be categorised as fit (n=360), pre-frail (n=579), or frail (n=138). Dr Salas mentioned that frail patients were not necessarily older than fit patients, but that they had a higher disease activity. Next to that, frail patients were significantly more likely to have fungal infections at 1 year of follow-up (10.9%) than pre-frail patients (4.6%) or fit patients (4.0%; P=0.004). “The cumulative incidence of ICU admission was also higher among frail patients [20.3%] than among pre-frail or fit patients [10.8%; 7.0%; P=0.002].” Furthermore, it was mentioned that the 2-year OS rates were 82%, 73%, and 62% in fit, pre-frail, and frail patients, respectively (P<0.001). Likewise, 2-year non-relapse mortality rates were lower in fit patients than in pre-frail or frail patients (12%, 20%, and 32%). “A multivariate analysis showed that the HCT-FS was an independent predictor for OS, with an increased risk of mortality in frail [HR 2.15; P<0.001] and pre-frail patients [HR 1.38; P=0.012], compared with fit patients,” Dr Salas pointed out. “This result was consistent across age groups and number of comorbidities, illustrating the utility of this assessment.”
In conclusion, the HCT-FS was an independent predictor of transplant outcomes in patients deemed eligible for allogeneic HCT, potentially refining the selection procedure for this burdensome treatment.
- Queralt Salas M, et al. HCT frailty scale (HCT-FS) for assessing frailty in allogeneic hematopoietic cell transplant patients: results from a multicenter and prospective Canadian and Spanish initiative. LB4005, EHA2025 Congress, 12–15 June, Milan, Italy.
Medical writing support was provided by Robert van den Heuvel.
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Table of Contents: EHA 2025
Featured articles
Letter from the Editor
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
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
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