Prognostic impact of chromosomal changes at relapse after allogeneic hematopoietic cell transplantation for acute myeloid leukemia or myelodysplastic syndrome

Chromosome analysis is a powerful prognostic tool in myeloid malignancies. Recipients who experience relapse after allogeneic hematopoietic cell transplantation (allo-HCT) often show chromosomal changes between diagnosis and relapse. However, the clinical impact of chromosomal changes and the effica...

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Veröffentlicht in:Bone marrow transplantation (Basingstoke) 2022-05, Vol.57 (5), p.810-816
Hauptverfasser: Okada, Yosuke, Nakasone, Hideki, Nakamura, Yuhei, Kawamura, Masakatsu, Kawamura, Shunto, Takeshita, Junko, Yoshino, Nozomu, Misaki, Yukiko, Yoshimura, Kazuki, Matsumi, Shimpei, Gomyo, Ayumi, Kawamura, Toshikuni, Akahoshi, Yu, Kusuda, Machiko, Kameda, Kazuaki, Tanihara, Aki, Tamaki, Masaharu, Kimura, Shun-ichi, Kobayashi, Shinichi, Kako, Shinichi, Kimura, Fumihiko, Kanda, Yoshinobu
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Sprache:eng
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Zusammenfassung:Chromosome analysis is a powerful prognostic tool in myeloid malignancies. Recipients who experience relapse after allogeneic hematopoietic cell transplantation (allo-HCT) often show chromosomal changes between diagnosis and relapse. However, the clinical impact of chromosomal changes and the efficacy of post-relapse treatment according to chromosomal changes have not been fully investigated. We retrospectively analyzed 72 recipients who had experienced relapse after allo-HCT for acute myeloid leukemia or myelodysplastic syndrome. We categorized them into two groups: with or without clonal chromosomal changes at relapse after allo-HCT. Post-relapse survival was shorter in the clonal chromosomal change group (median 117 days vs 275 days, P  = 0.019). Moreover, acquisition of chromosome 7 abnormality or complex changes tended to be associated with inferior survival in a univariate analysis (median 92 days vs median 173 days, P  = 0.043), and this adverse impact was confirmed in a multivariate analysis (hazard ratio 2.07, P  = 0.024). The patterns of chromosomal changes from diagnosis to relapse after allo-HCT were heterogenous, and further investigations are required to clarify the effect of individual chromosomal changes.
ISSN:0268-3369
1476-5365
DOI:10.1038/s41409-022-01635-4