Grip strength predicts overall survival of patients with myelodysplastic syndrome in a multivariable model

N Nicholas Chornenki (1University of British Columbia, Vancouver, Canada) L Lisa Chodirker (1Sunnybrook Health Sciences Centre, Medical Oncology and Hematology, Toronto, Canada) L Lee Mozessohn (4Sunnybrook Health Sciences Centre, Division of Medical Oncology and Hematology, Toronto, Canada) S Signy Chow (Sunnybrook Health Sciences Center, Toronto, Canada) J James Kennedy (Acute Multidisciplinary Imaging and Interventional Centre, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom) J James England (3Sunnybrook Health Sciences Centre, Toronto, Canada) J Jennifer Teichman (2Sunnybrook Hospital Odette Cancer Centre, Toronto, Canada) M Matthew Cheung (4Institute of Clinical Evaluative Sciences (ICES), Toronto, Canada) M Michelle Geddes (2Tom Baker Cancer Centre, Calgary, Canada) M Mitchell Sabloff (5The Ottawa Hospital, Ottawa, Canada) G Grace Christou (3The Ottawa Hospital, Ottawa, Canada) E Eve St-Hilaire (24Dr. Georges-L.-Dumont University Hospital Centre, Moncton, Canada) N Nicholas Finn (4Dr. Georges-L.-Dumont University Hospital Centre, Moncton, Canada) N Nancy Zhu (5University of Alberta Hospital, Edmonton, Canada) B Brian Leber (10Department of Medicine, McMaster University, Hamilton, Canada) A Alejandro Garcia-Horton (2Department of Oncology, McMaster University, Hamilton, Canada) A Amy Trottier (10Dalhousie University, Halifax, Canada) A April Shamy (8Jewish General Hospital, Montreal, Canada) H Heather Leitch (9St. Paul's Hospital, Vancouver, Canada) B Brett Houston (1University of Manitoba, Winnipeg, Canada) I Ivan Landego (10Cancer Care Manitoba, Winnipeg, Canada) K Karen W.L. Yee (1Princess Margaret Cancer Centre, Department of Medical Oncology and Hematology, Toronto, Canada) T Thomas Nevill (1University of British Columbia, Vancouver, Canada) J John Storring (13MUHC, Montreal, Canada) M Mohamed Elemary (6Saskatoon Cancer Agency, University of Saskatchewan, Saskatoon, Canada) L Laura Anne Habib (16St. Mary's Hospital, Montreal, Canada) R Robert Delage (Quebec CML-MPN Research Group, Montreal, Canada; Integrated Cancer Center, CHU de Québec, Laval University, Quebec, Canada) M Mohammed Siddiqui (2Sunnybrook Hospital Odette Cancer Centre, Toronto, Canada) L Liying Zhang (Ministry of Education Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology, Department of Chemistry) R Rena Buckstein

Abstract

Abstract Background: Myelodysplastic syndrome (MDS) is a clonal hematologic disorder characterized by cytopenias and a risk of progression to leukemia. Frailty, a state of reduced physiologic reserve, is prevalent among older individuals and is common in patients with MDS. MDS specific frailty scores such as the FS-15 can refine existing prognostic disease models. Physical function markers such as grip strength are frequently used to assess physical performance as a marker of frailty. In other cancer populations, grip strength predicts disease-specific mortality and cardiovascular disease. However, a paucity of data exists on the relationship between markers of physical performance and MDS outcomes, particularly when other disease markers and functional evaluations are considered. The aim of the present study was to determine the value of physical function testing in predicting the survival of patients with MDS. Methods: We conducted a retrospective cohort analysis of patients prospectively enrolled in the MDS-CAN registry (NCT02537990). The MDS-CAN registry (2006 to present) includes patients ≥ 18 years old with a diagnosis of MDS, MDS/MPN, or low blast count AML (20-30%). Grip strength, 10 x sit-stand test, and 4 meter walk test were collected as markers of physical performance. Grip strength was measured with a handheld dynamometer and was calculated as the average of three readings of the patient's dominant hand, stratified by sex. Survival analysis was performed by Kaplan-Meier analysis. Multivariable logistic regression models for overall survival were developed with backwards elimination. Results: A total of 1372 patients were included in the study, with a mean age at enrollment of 73.46 (SD 10.04) years. Most (896/1372; 65.31%) were male, while 529 (38.56%) received treatment with a hypomethylating agent. At a median follow-up of 2.8 years, 831 patients (60.57%) had died. 1022 patients had available grip strength data. Stratified by quartile, actuarial median overall survival (OS) (95% CI) was 23.6 months (19.1–27.9) for the lowest 25%, 28.2 months (22.4–39.9) for the 25th to 50th percentile, 38.9 months (29.2–47.1) for the 50th to 75th percentile, and 45 months (32.8-56.2) for the highest 25%. Reduced grip strength at baseline was associated with worse overall survival (Log-rank test p<.0001). These significant differences in overall survival were observed in longer term follow-up with 5-year OS of 39.3% (34.8-44.3%) in patients with grip strength above the median compared to 27.5% (23.1-32.7%) in patients with grip strength below the median. A 4 meter walk test faster than the median was associated with an actuarial median OS of 41.27 months (34.0-48.7), exceeding patients slower than median with actuarial median OS of 25.79 (23.0-30.2). A Stand-Sit test time below the median was associated with significantly higher actuarial median OS at 44.8 months (36.8-56.6) compared to 32.6 (25.9-37.6) months. Multivariable analysis included patient and disease-specific factors significant in univariate analysis. Grip strength measured at baseline below the median value retained an independent significant effect on OS measured from time of enrollment in multivariable analysis (HR 1.37 [1.11-1.69]). This multivariable analysis included the FS-15 assessment of frailty with HR 2.58 [1.93-3.43]) for scores of 0.26-0.6 vs. 0-0.25, HR 4.55 [2.40-8.65] for scores of 0.61-1.0 vs. 0-0.25, and HR 2.60 [1.54-4.37] for scores of 0.61-1.0 vs. 0.26-0.6. Other factors significant in multivariable analysis were QLQ-C30 Fatigue score below median (HR 0.75 [0.60-0.94]), higher ferritin (HR 1.13 [1.03-1.24]), IPSS-R (High Vs Low: HR 3.88 [3.01-5.00] Int vs low: HR 2.02 [1.55-2.65] High vs Int: HR 1.92 [1.48-2.48]), and MDS-Comorbidity index(HR 1.52 [1.22-1.9] for 1-2 vs 0 and HR 1.71 [1.18-2.48] for 3+ vs 0). Conclusion: Our study provides evidence that grip strength, an easy to obtain measure of physical functioning, predicts survival in MDS patients. We again validate the important prognostic impact of patient reported outcomes and patient-related factors that refine the prognosis of IPSS-R. Further research is warranted in assessing the impact of grip strength on treatment responses and tolerability in a longitudinal analysis.

Article Details

Journal Blood
Volume / Issue Vol. 146, Issue Supplement 1
Published November 03, 2025
Pages 964-964
ISSN 0006-4971
Publisher Elsevier BV

Journal Info

Blood

Elsevier BV

ISSN: 0006-4971 Health Sciences

Authors (30)

N

Nicholas Chornenki

1University of British Columbia, Vancouver, Canada

L

Lisa Chodirker

1Sunnybrook Health Sciences Centre, Medical Oncology and Hematology, Toronto, Canada

L

Lee Mozessohn

4Sunnybrook Health Sciences Centre, Division of Medical Oncology and Hematology, Toronto, Canada

S

Signy Chow

Sunnybrook Health Sciences Center, Toronto, Canada

J

James Kennedy

Acute Multidisciplinary Imaging and Interventional Centre, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom

J

James England

3Sunnybrook Health Sciences Centre, Toronto, Canada

J

Jennifer Teichman

2Sunnybrook Hospital Odette Cancer Centre, Toronto, Canada

M

Matthew Cheung

4Institute of Clinical Evaluative Sciences (ICES), Toronto, Canada

M

Michelle Geddes

2Tom Baker Cancer Centre, Calgary, Canada

M

Mitchell Sabloff

5The Ottawa Hospital, Ottawa, Canada

G

Grace Christou

3The Ottawa Hospital, Ottawa, Canada

E

Eve St-Hilaire

24Dr. Georges-L.-Dumont University Hospital Centre, Moncton, Canada

N

Nicholas Finn

4Dr. Georges-L.-Dumont University Hospital Centre, Moncton, Canada

N

Nancy Zhu

5University of Alberta Hospital, Edmonton, Canada

B

Brian Leber

10Department of Medicine, McMaster University, Hamilton, Canada

A

Alejandro Garcia-Horton

2Department of Oncology, McMaster University, Hamilton, Canada

A

Amy Trottier

10Dalhousie University, Halifax, Canada

A

April Shamy

8Jewish General Hospital, Montreal, Canada

H

Heather Leitch

9St. Paul's Hospital, Vancouver, Canada

B

Brett Houston

1University of Manitoba, Winnipeg, Canada

I

Ivan Landego

10Cancer Care Manitoba, Winnipeg, Canada

K

Karen W.L. Yee

1Princess Margaret Cancer Centre, Department of Medical Oncology and Hematology, Toronto, Canada

T

Thomas Nevill

1University of British Columbia, Vancouver, Canada

J

John Storring

13MUHC, Montreal, Canada

M

Mohamed Elemary

6Saskatoon Cancer Agency, University of Saskatchewan, Saskatoon, Canada

L

Laura Anne Habib

16St. Mary's Hospital, Montreal, Canada

R

Robert Delage

Quebec CML-MPN Research Group, Montreal, Canada; Integrated Cancer Center, CHU de Québec, Laval University, Quebec, Canada

M

Mohammed Siddiqui

2Sunnybrook Hospital Odette Cancer Centre, Toronto, Canada

L

Liying Zhang

Ministry of Education Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology, Department of Chemistry

R

Rena Buckstein