| Literature DB >> 34331021 |
Yu Akahoshi1, Yasuyuki Arai2, Satoshi Nishiwaki3, Takayoshi Tachibana4, Akihito Shinohara5, Noriko Doki6, Naoyuki Uchida7, Masatsugu Tanaka4, Yoshinobu Kanda8,9, Souichi Shiratori10, Yukiyasu Ozawa11, Katsuhiro Shono12, Yuta Katayama13, Junji Tanaka5, Takahiro Fukuda14, Yoshiko Atsuta15,16, Shinichi Kako8.
Abstract
White blood cell count (WBC) at diagnosis is the conventional prognostic factor in Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL). Nevertheless, little is known about the impact of WBC at diagnosis considering the minimal residual disease (MRD) status at allogeneic hematopoietic cell transplantation (HCT). We evaluated adult patients with Ph+ ALL who achieved negative-MRD and received HCT in first complete remission between 2006 and 2018. The entire cohort was temporally divided into derivation (n = 258) and validation cohorts (n = 366). Using a threshold of 15,000/μL, which was determined by a receiver operating characteristic curve analysis in the derivation cohort, high WBC was associated with an increased risk of hematological relapse in both the derivation cohort (25.3% vs. 11.6% at 7 years, P = 0.004) and the validation cohort (16.2% vs. 8.5% at 3 years, P = 0.025). In multivariate analyses, high WBC was a strong predictor of hematological relapse in the derivation cohort (HR, 2.52, 95%CI 1.32-4.80, P = 0.005) and in the validation cohort (HR, 2.32, 95%CI, 1.18-4.55; P = 0.015). In conclusion, WBC at diagnosis with a new threshold of 15,000/μL should contribute to better risk stratification in patients with negative-MRD at HCT.Entities:
Mesh:
Year: 2021 PMID: 34331021 DOI: 10.1038/s41409-021-01422-7
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.174