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Outcomes of transplant-eligible patients with myelodysplastic syndrome with excess blasts registered in a prospective observational study: The JALSG-CS11-MDS-SCT

Authors :
Ken Ishiyama
Noriharu Nakagawa
Kensuke Usuki
Satoru Takada
Tatsuki Tomikawa
Hiroshi Handa
Yuna Katsuoka
Daiki Hirano
Nobuo Sezaki
Masahiko Sumi
Shin Fujisawa
Yasuhiro Taniguchi
Atsuko Mugitani
Takuro Yoshimura
Eiichi Ohtsuka
Ken Takase
Youko Suehiro
Shuichi Ota
Tomohiro Kajiguchi
Tomoya Maeda
Masahide Yamamoto
Shigeki Ohtake
Akira Katsumi
Hitoshi Kiyoi
Itaru Matsumura
Yasushi Miyazaki
Publication Year :
2022
Publisher :
Research Square Platform LLC, 2022.

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-SCT) is the sole curative therapy for myelodysplastic syndromes (MDS). However, whether bridging therapy (BRT) including azacitidine (AZA) and combination chemotherapy (CCT) prior to allo-SCT should be performed is unclear. We analyzed BRT and the outcomes of patients with myelodysplastic syndrome with excess blasts (MDS-EB) who were registered in a prospective observational study in order to clarify the optimal allo-SCT strategy for high-risk MDS. A total of 371 patients were included in this study. Among 188 patients (50.7%) who were considered for allo-SCT, 141 actually underwent allo-SCT. Among the patients who underwent allo-SCT, 64 received AZA, 29 received CCT and 26 underwent allo-SCT without BRT as an initial treatment. The multivariate analysis identified BRT as independent factors influencing overall survival (AZA vs. without BRT, hazard ratio [HR] 3.33, 95% confidence interval [95%CI] 1.44–7.70, P = 0.005; CCT vs. without BRT, HR 3.82, 95%CI 1.60–9.14, P = 0.003). In a multivariate analysis, BRT showed an independent association with progression-free survival (AZA vs. without BRT, HR 2.23, 95%CI 1.03–4.83, P = 0.041; CCT vs. without BRT, HR 2.94, 95%CI 1.29–6.69, P = 0.010). Transplant-eligible patients with MDS-EB should undergo upfront allo-SCT without BRT.

Details

Database :
OpenAIRE
Accession number :
edsair.doi...........b739a6d580d7bb7f9e5237a9f936326c