Survival impact of post-transplant tyrosine kinase inhibitor therapy in chronic myeloid leukemia.

M Muhammad Mujtaba Bhinder (Charleston Area Medical Center (CAMC), Charleston, WV) H Haris Sohail (1Department of Hematology/Oncology, Charleston Area Medical Center, Charleston, WV) J Jennifer Collins (1Charleston Area Medical Center, Charleston, United States) S Salah Ud Din Safi (1West Virginia University School of Medicine, Internal Medicine, Morgantown, United States) A Amir Kamaran (Charleston Area Medical Center, Charleston, WV)

Abstract

e18599 Background: Although tyrosine kinase inhibitors (TKIs) have reduced the need for allogeneic hematopoietic stem cell transplantation (allo-HSCT) in chronic myeloid leukemia (CML), transplantation remains necessary for patients with TKI resistance, intolerance, or disease progression. Post-transplant TKI maintenance is widely used, yet real-world data evaluating its impact on overall survival (OS) and graft-versus-host disease (GVHD) are limited. We assessed the association between post-HSCT TKI use and long-term survival and GVHD outcomes. Methods: Adult CML patients undergoing allo-HSCT between January 2010 and June 2025 were identified in the TriNetX Research Network and categorized by TKI exposure within 3 months post-transplant. Cohorts were propensity score matched 1:1. OS was evaluated using Kaplan–Meier and Cox regression for 3 and 5 years. A landmark analysis beginning on day 30 was performed to address immortal time bias. Secondary outcomes included chronic GVHD within 1 year. Results: After matching, 350 patients were included (175 TKI vs 175 no TKI). At 3 years from transplant (day 0), OS was significantly higher with TKI therapy (72.67% vs 58.90%; HR 0.57, 95% CI 0.389–0.837; log-rank p=0.0036), with consistent landmark results (73.51% vs 59.93%; HR 0.566, 95% CI 0.383–0.838; p=0.0040). At 5 years, OS remained superior (68.75% vs 55.31%; HR 0.588, 95% CI 0.407–0.851; p=0.0043), with similar landmark findings (69.55% vs 56.27%; HR 0.585, 95% CI 0.402–0.853; p=0.0048). Chronic GVHD within 1 year was more frequent among TKI-treated patients (37.14% vs 24.57%; OR 1.81, 95% CI 1.14–2.88; p=0.011). Conclusions: Post-transplant TKI therapy was associated with significantly improved 3- and 5-year OS in patients with CML undergoing allo-HSCT, including landmark analysis. Higher rates of chronic GVHD may reflect confounding by indication and longer survival rather than a direct causal effect. These findings support post-HSCT TKI maintenance as an important survival-enhancing strategy in CML.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (5)

M

Muhammad Mujtaba Bhinder

Charleston Area Medical Center (CAMC), Charleston, WV

H

Haris Sohail

1Department of Hematology/Oncology, Charleston Area Medical Center, Charleston, WV

J

Jennifer Collins

1Charleston Area Medical Center, Charleston, United States

S

Salah Ud Din Safi

1West Virginia University School of Medicine, Internal Medicine, Morgantown, United States

A

Amir Kamaran

Charleston Area Medical Center, Charleston, WV