Post-transplant TKIs for Ph+ ALL: practices to date and clinical significance

Post-transplant tyrosine kinase inhibitors (TKIs) show promise in preventing relapse after allogeneic hematopoietic cell transplantation (allo-HCT) for Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL). However, their real-world use and efficacy remain unclear. A comprehensive s...

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Veröffentlicht in:International journal of hematology 2025-01
Hauptverfasser: Nishiwaki, Satoshi, Terakura, Seitaro, Morishita, Takanobu, Goto, Tatsunori, Inagaki, Yuichiro, Miyao, Kotaro, Fukushima, Nobuaki, Hirano, Daiki, Tange, Naoyuki, Kurahashi, Shingo, Kuwatsuka, Yachiyo, Kasai, Masanobu, Iida, Hiroatsu, Ozeki, Kazutaka, Sawa, Masashi, Nishida, Tetsuya, Kiyoi, Hitoshi
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Sprache:eng
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Zusammenfassung:Post-transplant tyrosine kinase inhibitors (TKIs) show promise in preventing relapse after allogeneic hematopoietic cell transplantation (allo-HCT) for Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL). However, their real-world use and efficacy remain unclear. A comprehensive study across seven centers included Ph+ALL patients who underwent allo-HCT between 2002 and 2022. Post-transplant TKIs were administered in 28% of patients (49 of 173 transplanted in complete remission): 7% as prophylaxis during complete molecular remission (CMR), and 21% in response to measurable residual disease (MRD) positivity. Median first post-transplant TKI duration was 13.7 months for the prophylactic group and 4.0 months for the MRD-triggered group. Prophylactic TKIs appear particularly beneficial for patients not in CMR at allo-HCT, showing a trend towards higher 5-year relapse-free survival (RFS) compared to those not receiving prophylactic TKIs (100% vs. 73%; P = 0.11). Significant RFS differences were observed between the prophylactic, non-TKI, and MRD-triggered groups. However, patients with white blood cell counts
ISSN:0925-5710
1865-3774
1865-3774
DOI:10.1007/s12185-025-03917-1