-Author name in bold denotes the presenting author
-Asterisk * with author name denotes a Non-ASH member
Clinically Relevant Abstract denotes an abstract that is clinically relevant.

PhD Trainee denotes that this is a recommended PHD Trainee Session.

Ticketed Session denotes that this is a ticketed session.

3510 Frailty Syndrome Is Associated with Increased Endothelial Activation and Post-Transplant Complications in Allo-HCT Patients

Program: Oral and Poster Abstracts
Session: 721. Allogeneic Transplantation: Conditioning Regimens, Engraftment, and Acute Toxicities: Poster II
Hematology Disease Topics & Pathways:
Research, Translational Research, Clinical Practice (Health Services and Quality), Clinical Research, Health outcomes research, Supportive Care, Diseases, Treatment Considerations, Survivorship
Sunday, December 8, 2024, 6:00 PM-8:00 PM

Maria Queralt Salas, MD, PhD1*, Julia Martinez-Sanchez, PhD2*, Raquel Salinas González, MD3*, Blanca de Moner4*, ANA Belen MORENO Castaño, MD5*, Silvia Escribano-Serrat, MD5*, Alex Ramos6*, Carla Mestre7*, Cristina Padilla8*, Laia Guardia9*, Filipe Pinto, MD9*, Paola Charry, MD10*, Joan Cid, MD PhD11*, Miquel Lozano, MD, PhD12*, Enric Cascos, MD13*, Jordi Esteve, MD, PhD14, Sara Laxe, MD15*, Concepción Closa, MD15*, Enric Carreras, MD, PhD16*, Maria Suarez-Lledo, MD, PhD17*, Laura Rosiñol Dachs, MD PhD18*, Francesc Fernández-Avilés, MD, PhD19*, Montserrat Rovira, MD, PhD19*, Maria Carmen Martinez Munoz, MD, PhD20* and Maribel Diaz-Ricart, PhD2*

1Hematopoietic Transplantation Unit, Hospital Clinic de Barcelona, ICAMS, Barcelona, Spain
2Hemostasis and Erythropathology, Hematopathology, Pathology Department, CDB, IDIBAPS, University of Barcelona, Hospital Clínic de Barcelona, Barcelona, Spain
3Physical Medicine and Rehabilitation Department, Hospital Clinic de Barcelona, Barcelona, Spain
4Hospital Clinic de Barcelona, Ba, Spain
5Hospital Clinic Barcelona, Barcelona, Spain
6Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS. Hospital Clinic de Barcelona, Barcelona, Spain
7Endocrinology and Nutrition Department, Hospital Clinic of Barcelona, Barcelona, Spain
8Hospital Clinic of Barcelona, Barcelona, ESP
9Hematopoietic Transplantation Unit, Hematology Department, Clinical Institute of Hematology and Oncology (ICMHO), Hospital Clinic de Barcelona, Barcelona, Spain
10Apheresis and Cellular Therapy Unit, Hemotherapy and Hemostasis Department, Clinical Institute of Hematology and Oncology (ICMHO), Hospital Clinic de Barcelona, Barcelona, Spain
11Hospital Clinic, University of Barcelona, Barcelona, Spain
12Apheresis and Cellular Therapy Unit, Hemotherapy and Hemostasis Department, Clinical Institute of Hematology and Oncology (ICMHO), Hospital Clínic de Barcelona, Barcelona, Spain
13Cardiology Department, Hospital Clinic de Barcelona, Barcelona, Spain
14Hematology Department, Hospital Clínic Barcelona, ICAMS, Barcelona, Spain
15Physical Medicine and Rehabilitation Department, Hospital Clinic of Barcelona, Barcelona, Spain
16Fundació Josep Carreras Contra la Leucèmia, Barcelona, Spain
17Hematopoietic Transplantation Unit, Hematology Department, Clinical Institute of Hematology and Oncology (ICMHO), Spain, Hospital Clínic de Barcelona, Barcelona, Spain
18Hematopoietic Cell Transplant Unit, Hospital Clínic de Barcelona, ICAMS, Barcelona, Spain
19Hematopoietic Transplantation Unit, Hematology Department, Clinical Institute of Hematology and Oncology (ICMHO), Hospital Clínic de Barcelona, Barcelona, Spain
20Hematopoietic Cell Transplant Unit, Hospital Clinic of Barcelona, ICAMS, Barcelona, Spain

Introduction

Frailty increases mortality and morbidity risks in allo-HCT patients, but its pathophysiological mechanisms remain under-studied. Previous research has linked chronic inflammation, endothelial activation and dysfunction, and frailty, particularly in older adults and those at cardiovascular risk. Given that endothelial activation -and dysfunction- occurs early post-allo-HCT due to the conditioning regimen, GVHD prophylaxis, alloreactivity, and transplant complications, this study investigates whether frailty syndrome may influence these processes.

Methods

From 2021 to 2023, 128 allo-HCT consecutive adults were included in the study. Patients were evaluated using the HCT Frailty Scale and categorized as fit, pre-frail, or frail based on the results.

Endothelial activation was indirectly measured in all patients using the Endothelial Activation and Stress Index (EASIX), calculated from bloodworks collected at admission and on days 0, +7, +14, +21, +28, +100, and +180 after transplantation. EASIX data was complemented with the measurement of circulating endothelial activation biomarkers (von Willebrand factor antigen (VWF), soluble vascular cell adhesion molecule-1 (VCAM), regenerating islet-derived 3-alpha (REG3α), soluble tumor necrosis factor receptor I (sTNFRI), and thrombomodulin (TM)) in plasma samples of 48 consecutive patients collected at admission.

Clinical information and frailty prospective data was merged with EASIX and biomarker determinations.

Results

The cohort median age was 55 years (IQR: 41-64), with 87 (68.0%) male patients. 31 (24.2%) had a KPS <90%, and 26 (20.3%) had an HCT-CI >3. AML was the most prevalent baseline diagnosis (n=30, 31.3%). 61(47.7%) patients underwent MAC allo-HCT, and 125 (97.7%) received peripheral blood grafts: 78 (61.0%) from HLA-matched, 24 (18.8%) from 9/10 HLA-mismatched unrelated, and 26 (20.3%) from haploidentical donors.

At HCT admission, 19 (14.8%) patients were classified as frail, 61 (47.7%) as pre-frail, and 48 (37.5%) as fit. Although not statistically significant, proportions of veno-occlusive disease (11.1%, 1.6% and 2.1%, p=0.185) and transplant-associated thrombotic microangiopathy (11.1%, 4.9% and 2.1%, p=0.479) were higher in frail patients than in pre-frail and fit ones, respectively. Overall, clinically relevant aGVHD (frail and pre-frail vs. fit: Grades II-IV aGVHD: HR 5.11, P<0.01; Grades III-IV aGVHD: HR 3.64, P=0.091), cardiac events (frail and pre-frail vs. fit: HR 3.95, P=0.073), ICU admissions (frail and pre-frail vs. fit: HR 2.63, P=0.084) trend to be higher in frail and pre-frail patients than in fit ones.

With a median follow-up of 15 months, 30 (23.4%) patients relapsed and 34 (26.5%) dead. Frailty was associated with worse outcomes, with 1-year OS rates for frail, pre-frail and fit patients of 40.0%, 76.7% and 85.2% (p=0.017), and respective 1-year NRM of 33.3%, 15.2% and 10.4% (P=0.269).

At admission, EASIX medians were higher in frail patients than in pre-frail and fit ones, (Frail, Pre-frail, Fit patients: 1.50, 1.32, 0.82, P=0.010). The complementary analysis of the 48 patients' samples at HCT admission – moment at which 6 patients were frail, 21 pre-frail and 21 fit- revealed that frail patients had higher median values of VWF (frail, pre-frail and fit: 149, 138 and 122 U/dl, respectively), REG3α (19.5, 17.3 and 13.9 ng/dl), and VCAM (156.9, 55.2 and 85.8 ng/dl), and lower TM levels (3.1, 4.0, 4.9 ng/dl) than pre-frail and fit ones, and suggesting that frail patients had higher endothelial activation than the rest.

EASIX trends according to the frailty state of patients were examined in all patients showing that EASIX globally increased from day 0 to day +7, peaked at day +21, and declined progressively by day +180. However, EASIX medians were higher in frail patients than in fit ones, and with a higher peak at day +21 than in pre-frail and fit ones (median values: 8.4, 6.8 and 5.4).

Conclusions

The study shows that frailty is associated with increased endothelial activation and post-transplant complications in allo-HCT patients. Although complications were more prevalent in pre-frail and frail patients, frail patients had higher mortality, indicating their limited capacity to overcome complications.

Frailty should be considered when assessing and managing allo-HCT patients, and further exploring how frailty influences outcomes through endothelial activation will be valuable.

Disclosures: Cid: Sanofi: Consultancy, Research Funding; Clínic Barcelona: Current Employment. Rosiñol Dachs: BMS, Takeda, Pfizer, Menarini: Honoraria; GSK: Honoraria, Other: Honoraria for lectures; Sanofi: Honoraria, Other: Honoraria for lectures; Amgen: Honoraria, Other: Educational lectures; Janssen Pharmaceutica: Honoraria, Other: Honoraria for lectures and meeting travel support. Martinez Munoz: Sanofi: Membership on an entity's Board of Directors or advisory committees; Novartis: Research Funding; Takeda: Membership on an entity's Board of Directors or advisory committees. Diaz-Ricart: Jazz Pharmaceuticals and Sanofi,: Speakers Bureau; Novartis Spain, CSL Behring, and Sysmex Europe GmbH.: Research Funding.

*signifies non-member of ASH