Literature DB >> 27154847

Filgrastim-Stimulated Bone Marrow Compared with Filgrastim-Mobilized Peripheral Blood in Myeloablative Sibling Allografting for Patients with Hematologic Malignancies: A Randomized Canadian Blood and Marrow Transplant Group Study.

Stephen Couban1, Mahmoud Aljurf2, Sylvie Lachance3, Irwin Walker4, Cynthia Toze5, Morel Rubinger6, Jeffrey H Lipton7, Stephanie J Lee8, Jeff Szer9, Richard Doocey10, Ian D Lewis11, Lothar Huebsch12, Kang Howson-Jan13, Michel Lalancette14, Fahad Almohareb2, Nadeem Chaudhri2, Sabine Ivison15, Raewyn Broady5, Megan Levings15, Diane Fairclough16, Gerald Devins7, David Szwajcer6, Ronan Foley4, Clayton Smith16, Tony Panzarella7, Holly Kerr5, Amina Kariminia15, Kirk R Schultz15.   

Abstract

In adult hematopoietic cell transplantation (HCT), filgrastim-mobilized peripheral blood (G-PB) has largely replaced unstimulated marrow for allografting. Although the use of G-PB results in faster hematopoietic recovery, it is also associated with more chronic graft-versus-host disease (cGVHD). A potential alternative allograft is filgrastim-stimulated marrow (G-BM), which we hypothesized may be associated with prompt hematopoietic recovery but with less cGVHD. We conducted a phase 3, open-label, multicenter randomized trial of 230 adults with hematologic malignancies receiving allografts from siblings after myeloablative conditioning to compare G-PB with G-BM. The primary endpoint was time to treatment failure, defined as a composite of extensive cGVHD, relapse/disease progression, and death. With a median follow-up of 36 months (range, 9.6 to 48), comparing G-BM with G-PB, there was no difference between the 2 arms with respect to the primary outcome of this study (hazard ratio [HR], .91; 95% confidence interval [CI], .68 to 1.22; P = .52). However, the cumulative incidence of overall cGVHD was lower with G-BM (HR, .66; 95% CI, .46 to .95; P = .007) and there was no difference in the risk of relapse or progression (P = .35). The median times to neutrophil recovery (P = .0004) and platelet recovery (P = .012) were 3 days shorter for recipients allocated to G-PB compared with those allocated to G-BM, but there were no differences in secondary engraftment-related outcomes, such as time to first hospital discharge (P = .17). In addition, there were no graft failures in either arm. This trial demonstrates that, compared with G-PB, the use of G-BM allografts leads to a significantly lower rate of overall cGVHD without a loss of the graft-versus-tumor effect and comparable overall survival. Our findings suggest that further study of this type of allograft is warranted.
Copyright © 2016 American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Blood and marrow transplantation; Donor source; Filgrastim; Graft-versus-host disease; Hematopoietic cell transplantation; Mobilized bone marrow

Mesh:

Substances:

Year:  2016        PMID: 27154847     DOI: 10.1016/j.bbmt.2016.04.017

Source DB:  PubMed          Journal:  Biol Blood Marrow Transplant        ISSN: 1083-8791            Impact factor:   5.742


  5 in total

Review 1.  The Biology of Chronic Graft-versus-Host Disease: A Task Force Report from the National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease.

Authors:  Kenneth R Cooke; Leo Luznik; Stefanie Sarantopoulos; Frances T Hakim; Madan Jagasia; Daniel H Fowler; Marcel R M van den Brink; John A Hansen; Robertson Parkman; David B Miklos; Paul J Martin; Sophie Paczesny; Georgia Vogelsang; Steven Pavletic; Jerome Ritz; Kirk R Schultz; Bruce R Blazar
Journal:  Biol Blood Marrow Transplant       Date:  2016-10-03       Impact factor: 5.742

2.  CD56bright natural killer regulatory cells in filgrastim primed donor blood or marrow products regulate chronic graft-versus-host disease: the Canadian Blood and Marrow Transplant Group randomized 0601 study results.

Authors:  Amina Kariminia; Sabine Ivison; Bernard Ng; Jacob Rozmus; Susanna Sung; Avani Varshney; Mahmoud Aljurf; Sylvie Lachance; Irwin Walker; Cindy Toze; Jeff Lipton; Stephanie J Lee; Jeff Szer; Richard Doocey; Ian Lewis; Clayton Smith; Naeem Chaudhri; Megan K Levings; Raewyn Broady; Gerald Devins; David Szwajcer; Ronan Foley; Sara Mostafavi; Steven Pavletic; Donna A Wall; Stephan Couban; Tony Panzarella; Kirk R Schultz
Journal:  Haematologica       Date:  2017-09-21       Impact factor: 9.941

3.  Influence of graft composition in patients with hematological malignancies undergoing ATG-based haploidentical stem cell transplantation.

Authors:  Ran Zhang; Xuan Lu; Liang V Tang; Huafang Wang; Han Yan; Yong You; Zhaodong Zhong; Wei Shi; Linghui Xia
Journal:  Front Immunol       Date:  2022-09-15       Impact factor: 8.786

4.  Neupogen and mesenchymal stem cells are the novel therapeutic agents in regeneration of induced endometrial fibrosis in experimental rats.

Authors:  Dina Sabry; Abeer Mostafa; Samar Marzouk; Walaa Ibrahim; Hanan H M Ali; Aymen Hassan; Ashraf Shamaa
Journal:  Biosci Rep       Date:  2017-10-11       Impact factor: 3.840

5.  Superior GVHD-free, relapse-free survival for G-BM to G-PBSC grafts is associated with higher MDSCs content in allografting for patients with acute leukemia.

Authors:  Qian Fan; Hui Liu; Xinquan Liang; Ting Yang; Zhiping Fan; Fen Huang; Yiwen Ling; Xin Liao; Li Xuan; Na Xu; Xiaojun Xu; Jieyu Ye; Qifa Liu
Journal:  J Hematol Oncol       Date:  2017-07-04       Impact factor: 17.388

  5 in total

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