The humanistic burden of patients with chronic myeloid leukemia (CML) treated with first line (1L) tyrosine kinase inhibitors (TKIs)

K Kelly Schoenbeck (1University of California, California, United States) J Joan Clements (2CML Buster Foundation, Costa Mesa, United States) K Karen Demairo (3The Leukemia & Lymphoma Society, LA, United States) D David Wei (5Novartis Pharmaceuticals Corporation, East Hanover, United States) N Nisha Hazra (5Analysis Group Inc, Montreal, Canada) C Cristina Constantinescu (6Ipsos, Geneva, Switzerland) Y Yan Meng (Marine Science and Technology Domain, Beijing Institute of Technology) D Dominick Latremouille-Viau G Gabriel Marquez (2Novartis Ireland Limited, Dublin, Ireland) D Daisy Yang (4Novartis Pharmaceuticals Corporation, East Hanover, United States) A Andrea Damon (4Novartis Pharmaceuticals Corporation, East Hanover, United States) I Islam Mohamad Sadek (5Novartis Pharmaceuticals Corporation, East Hanover, United States) A Annie Guerin (5Analysis Group Inc, Montreal, Canada) K Kathryn Flynn (1CIBMTR® (Center for International Blood and Marrow Transplant Research), Medical College of Wisconsin, Milwaukee, United States)

Abstract

Abstract INTRODUCTION: While TKIs significantly extend survival in CML, their adverse events (AEs) may lead to treatment discontinuation and poor health-related quality of life (HRQoL). Few studies have described the HRQoL of US patients (pts) on TKIs. This study assessed the humanistic burden of pts with CML treated with first-line (1L) TKIs, including their AE profile, HRQoL, and work productivity, using patient-reported outcomes. We also evaluated communication barriers between pts and treating physicians. METHODS: Cross-sectional online surveys were conducted (June-December 2024) among US CML pts. Adults receiving 1L TKIs (imatinib, dasatinib, nilotinib, bosutinib) for ≥3 months (mos) were eligible to participate; asciminib in 1L was not yet approved at study start. AE data were collected via PRO-CTCAE, and pts completed surveys on patient-physician communication about AEs. HRQoL was evaluated using the PROMIS-Global Health-10 (Global Physical Health [GPH] and Global Mental Health [GMH], general population mean±SD of 50±10, lower T-scores=poorer health), and Work Productivity and Activity Impairment: Specific Health Problem (WPAI:SHP, higher percentages=greater impairment) questionnaires. “Low points,” defined as the time(s) when AEs had the greatest impact on HRQoL, were also reported. RESULTS: A cohort of 162 pts (median age 45 yrs [range 18-82], 60% female, 19% non-White) treated with a 1L TKI (42% imatinib, 38% dasatinib, 11% nilotinib, 9% bosutinib) participated. Half were employed (51%; 21% retired, 15% not employed, 6% on disability) and treated in a community-based setting (54%; 41% academic, 5% other/unsure). Two-thirds were commercially insured (65%; 26% Medicare, 7% Medicaid, 2% military/unsure). Over half had been on 1L TKI for ≥1 yr (59%; 11% 3 to <6 mos, 30% 6 mos to <1 yr). In the last 7 days, pts reported a median of 3 AEs (range 0-14); most commonly, fatigue (51%), pain (45%; joint/muscle pain), and gastrointestinal (33%; nausea, diarrhea, vomiting, constipation). Three-quarters (75%) had ≥1 AE, mostly chronic, in the last 7 days. Most pts (82%) experienced low points since TKI start, most commonly in the first 3 mos of treatment (59%), with 24% reporting ≥1 low point in the last 7 days. Nearly all pts (98%) reported discussing AEs at least once with their physician, most frequently at diagnosis (72%) or at subsequent visits (75%); half (54%) discussed AEs at every visit. Two-thirds (64%) reported being satisfied with their discussions about AEs. However, some delayed or did not report AEs to their physicians (17%), for reasons that they “just had to live with it” (70%), were “afraid the doctor may decide to change treatment” (44%), or did not want to “be a burden” (33%). PROMIS-GH-10 revealed pts with CML had worse health than the general population, with mean±SD GPH T-score of 43.2±7.4 and GMH T-score of 43.9±7.6. Among pts with low points in the last 7 days, GPH and GMH T-scores were even worse (GPH: 37.5±6.5; GMH: 38.0±7.4). WPAI SHP showed over half (54%) of pts reported employment change due to CML (12% retired early, 11% from full- to part-time, 10% from full-time to unemployed, 8% stopped working temporarily or reduced workload), with an overall mean activity impairment of 35.1% (range 0-100%). Among those employed, 80% reported work impairment due to CML, with a mean percent work productivity loss of 29.9%. Mean impairment while working (presenteeism) and work time missed (absenteeism) due to CML were 27.2% and 7.6%, respectively. Pts with low points in the last 7 days had even higher mean activity impairment (52.8%) and work productivity loss (38.8%) due to CML. CONCLUSIONS:Our real-world study demonstrates pts with CML treated with 1L TKIs in the US experience chronic AEs contributing to worse HRQoL, including physical and mental health, as well as work impairment. This finding of impaired work productivity due to CML is particularly significant in the context of employer-provided health insurance in the US. While most patients discussed AEs with physicians early in their disease course, only half discussed AEs at every visit and two-thirds were satisfied with their discussions. In addition, some patients delayed or avoided reporting AEs due to internal barriers. As CML requires lifelong treatment, pts may benefit from greater recognition of AEs and strategies to improve HRQoL and maintain work productivity, including TKIs with better tolerability and more consistent approaches to monitoring.

Article Details

Journal Blood
Volume / Issue Vol. 146, Issue Supplement 1
Published November 03, 2025
Pages 6388-6388
ISSN 0006-4971
Publisher Elsevier BV

Journal Info

Blood

Elsevier BV

ISSN: 0006-4971 Health Sciences

Authors (14)

K

Kelly Schoenbeck

1University of California, California, United States

J

Joan Clements

2CML Buster Foundation, Costa Mesa, United States

K

Karen Demairo

3The Leukemia & Lymphoma Society, LA, United States

D

David Wei

5Novartis Pharmaceuticals Corporation, East Hanover, United States

N

Nisha Hazra

5Analysis Group Inc, Montreal, Canada

C

Cristina Constantinescu

6Ipsos, Geneva, Switzerland

Y

Yan Meng

Marine Science and Technology Domain, Beijing Institute of Technology

D

Dominick Latremouille-Viau

G

Gabriel Marquez

2Novartis Ireland Limited, Dublin, Ireland

D

Daisy Yang

4Novartis Pharmaceuticals Corporation, East Hanover, United States

A

Andrea Damon

4Novartis Pharmaceuticals Corporation, East Hanover, United States

I

Islam Mohamad Sadek

5Novartis Pharmaceuticals Corporation, East Hanover, United States

A

Annie Guerin

5Analysis Group Inc, Montreal, Canada

K

Kathryn Flynn

1CIBMTR® (Center for International Blood and Marrow Transplant Research), Medical College of Wisconsin, Milwaukee, United States