| Literature DB >> 25605541 |
Hiroaki Shimizu1, Takayuki Saitoh1, Shinichiro Machida2, Shinichi Kako3, Noriko Doki4, Takehiko Mori5, Toru Sakura6, Yoshinobu Kanda3, Heiwa Kanamori7, Shuichi Miyawaki8, Shinichiro Okamoto5.
Abstract
Adult patients with mixed phenotype acute leukemia (MPAL) have a poor prognosis, and the therapeutic role of allogeneic stem cell transplantation (allo-SCT) for MPAL remains to be elucidated. Thus, we retrospectively assessed the efficacy of allo-SCT for MPAL. Eighteen patients with MPAL were identified from the transplant outcome database of Kanto Study Group for Cell Therapy (KSGCT). We also selected 215 patients with acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) as control cohorts using an optimal matching method. The 5-yr overall survival (OS) rate of patients with MPAL was 48.1%, and patients in remission at the time of transplant showed significantly better survival than those not in remission (5-yr OS: 71.8% vs. 0%, P = 0.001). No significant differences were seen in OS when stratifying patients according to immunophenotype, cytogenetic abnormalities, or the type of induction therapy. The 5-yr OS rate of patients with MPAL was not significantly different compared with AML control patients (48.1% vs. 48.1%; P = 0.855) or ALL control patients (48.1% vs. 37.8%; P = 0.426). These results suggested that allo-SCT is an effective treatment for MPAL, especially early in the disease course, and innovative transplant approaches are warranted to improve the transplant outcome of patients with MPAL who are not in remission.Entities:
Keywords: Philadelphia chromosome; allogeneic hematopoietic stem cell transplantation; matched-pair analysis; mixed phenotype acute leukemia; outcomes
Mesh:
Year: 2015 PMID: 25605541 DOI: 10.1111/ejh.12516
Source DB: PubMed Journal: Eur J Haematol ISSN: 0902-4441 Impact factor: 2.997