| Literature DB >> 33864019 |
Mary-Elizabeth Percival1, Hai-Lin Wang2, Mei-Jie Zhang2,3, Wael Saber2, Marcos de Lima4, Mark Litzow5, Partow Kebriaei6, Hisham Abdel-Azim7, Kehinde Adekola8, Mahmoud Aljurf9, Ulrike Bacher10, Sherif M Badawy11,12, Amer Beitinjaneh13, Nelli Bejanyan14, Vijaya Bhatt15, Michael Byrne16, Jean-Yves Cahn17, Paul Castillo18, Nelson Chao19, Saurabh Chhabra2,20, Edward Copelan21, Corey Cutler22, Zachariah DeFilipp23, Ajoy Dias24, Miguel Angel Diaz25, Elihu Estey26, Nosha Farhadfar27, Haydar A Frangoul28, César O Freytes29, Robert Peter Gale30, Siddhartha Ganguly31, Lohith Gowda32, Michael Grunwald21, Nasheed Hossain33, Rammurti T Kamble34, Christopher G Kanakry35, Ankit Kansagra36, Mohamed A Kharfan-Dabaja37, Maxwell Krem38, Hillard M Lazarus39, Jong Wook Lee40, Jane L Liesveld41, Richard Lin42, Hongtao Liu43, Joseph McGuirk44, Reinhold Munker45, Hemant S Murthy37, Sunita Nathan46, Taiga Nishihori14, Richard F Olsson47,48, Neil Palmisiano49, Jakob R Passweg50, Tim Prestidge51, Olov Ringdén52, David A Rizzieri53, Witold B Rybka54, Mary Lynn Savoie55, Kirk R Schultz56, Sachiko Seo57, Akshay Sharma58, Melhem Solh59, Roger Strair60, Marjolein van der Poel61, Leo F Verdonck62, Jean A Yared63, Daniel Weisdorf64,65, Brenda M Sandmaier66.
Abstract
Acute myeloid leukemia (AML) patients often undergo allogeneic hematopoietic cell transplantation (alloHCT) in first complete remission (CR). We examined the effect of depth of clinical response, including incomplete count recovery (CRi) and/or measurable residual disease (MRD), in patients from the Center for International Blood and Marrow Transplantation Research (CIBMTR) registry. We identified 2492 adult patients (1799 CR and 693 CRi) who underwent alloHCT between January 1, 2007 and December 31, 2015. The primary outcome was overall survival (OS). Multivariable analysis was performed to adjust for patient-, disease-, and transplant-related factors. Baseline characteristics were similar. Patients in CRi compared to those in CR had an increased likelihood of death (HR: 1.27; 95% confidence interval: 1.13-1.43). Compared to CR, CRi was significantly associated with increased non-relapse mortality (NRM), shorter disease-free survival (DFS), and a trend toward increased relapse. Detectable MRD was associated with shorter OS, shorter DFS, higher NRM, and increased relapse compared to absence of MRD. The deleterious effects of CRi and MRD were independent. In this large CIBMTR cohort, survival outcomes differ among AML patients based on depth of CR and presence of MRD at the time of alloHCT. Further studies should focus on optimizing post-alloHCT outcomes for patients with responses less than CR.Entities:
Mesh:
Year: 2021 PMID: 33864019 PMCID: PMC8425595 DOI: 10.1038/s41409-021-01261-6
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.483