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Reappraising the prognostic relevance of cytogenetic risk in patients with acute myeloid leukemia undergoing allogeneic hematopoietic cell transplantation

  • Shohei Mizuno,
  • Hiroki Hosoi,
  • Akiyoshi Takami,
  • Takahito Kawata,
  • Noriko Doki,
  • Wataru Takeda,
  • Masatsugu Tanaka,
  • Tetsuya Nishida,
  • Naoyuki Uchida,
  • Yuta Hasegawa,
  • Masashi Sawa,
  • Shuichi Ota,
  • Makoto Onizuka,
  • Hirohisa Nakamae,
  • Noboru Asada,
  • Takahiro Fukuda,
  • Makoto Yoshimitsu,
  • Yoshinobu Kanda,
  • Marie Ohbiki,
  • Yoshiko Atsuta,
  • Takaaki Konuma,
  • Masamitsu Yanada

摘要

This study aimed to investigate the prognostic relevance of cytogenetic risk in 9826 adults with acute myeloid leukemia (AML) who underwent allogeneic hematopoietic cell transplantation (HCT) during the first or second complete remission. The 5-year probabilities of overall survival (OS) were 66%, 61%, and 47% (P < 0.001), the cumulative incidences of relapse were 14%, 19%, and 32% (P < 0.001), and the cumulative incidences of non-relapse mortality (NRM) were 23%, 23%, and 25% (P = 0.208) in patients with favorable (n = 1418), intermediate (n = 6747), and poor cytogenetic risk (n = 1661), respectively. The significant effect of cytogenetic risk on OS was strong in all subgroups stratified by age, sex, performance status, disease status, donor type, conditioning intensity, graft-versus-host disease prophylaxis, and transplantation period (P < 0.001 for all). The evaluation of trends in posttransplant outcomes for patients in each cytogenetic risk category indicated that the risk of relapse declined in patients with favorable and intermediate cytogenetics and that the risk of NRM decreased in those with intermediate and poor cytogenetics. Therefore, patients with intermediate cytogenetics experienced the best OS improvement. These results confirm cytogenetic risk as a universal prognostic factor in patients with AML undergoing allogeneic HCT while highlighting the requirement for further improvements in posttransplant OS by reducing NRM in patients with favorable cytogenetics and by reducing relapse in patients with poor cytogenetics.