Predictors of recovery following allogeneic CD34+-selected cell infusion without conditioning to correct poor graft function.


Journal

Haematologica
ISSN: 1592-8721
Titre abrégé: Haematologica
Pays: Italy
ID NLM: 0417435

Informations de publication

Date de publication:
01 11 2020
Historique:
aheadofprint: 21 11 2019
entrez: 2 11 2020
pubmed: 3 11 2020
medline: 28 4 2021
Statut: epublish

Résumé

Poor graft function is a serious complication following allogeneic hematopoietic stem cell transplantation. Infusion of CD34+-selected stem cells without pre-conditioning has been used to correct poor graft function, but predictors of recovery are unclear. We report the outcome of 62 consecutive patients who had primary or secondary poor graft function who underwent a CD34+-selected stem cell infusion from the same donor without further conditioning. Forty-seven of 62 patients showed hematological improvement and became permanently transfusion and growth factor-independent. In multivariate analysis, parameters significantly associated with recovery were shared CMV seronegative status for recipient/donor, the absence of active infection and matched recipient/donor sex. Recovery was similar in patients with mixed and full donor chimerism. Five -year overall survival was 74.4% (95% CI 59-89) in patients demonstrating complete recovery, 16.7% (95% CI 3-46) in patients with partial recovery and 22.2% (CI 95% 5-47) in patients with no response. In patients with count recovery, those with poor graft function in 1-2 lineages had superior 5-year overall survival (93.8%, 95% CI 82-99) than those with tri-lineage failure (53%, 95% CI 34-88). New strategies including cytokine or agonist support, or second transplant need to be investigated in patients who do not recover.

Identifiants

pubmed: 33131253
doi: 10.3324/haematol.2019.226340
pmc: PMC7604618
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2639-2646

Auteurs

Maria M Cuadrado (MM)

Anthony Nolan Research Institute, London;.

Richard M Szydlo (RM)

Department of Haematology, Imperial College London;.

Mike Watts (M)

Cellular Therapeutics, University College London.

Nishil Patel (N)

Department of Hematology, Royal Free London NHS Trust, London.

Hanna Renshaw (H)

Department of Hematology, Royal Free London NHS Trust, London.

Jude Dorman (J)

Department of Hematology, University College Hospital NHS Trust, London.

Mark Lowdell (M)

Department of Hematology, University College Hospital NHS Trust, London.

Stuart Ings (S)

Cellular Therapeutics, University College London.

Chloe Anthias (C)

Anthony Nolan Research Institute, London.

Alejandro Madrigal (A)

Anthony Nolan Research Institute, London.

Stephen Mackinnon (S)

Department of Hematology, University College Hospital NHS Trust, London.

Panagiotis Kottaridis (P)

Department of Hematology, University College Hospital NHS Trust, London.

Ben Carpenter (B)

Department of Hematology, University College Hospital NHS Trust, London.

Rachael Hough (R)

Department of Hematology, University College Hospital NHS Trust, London.

Emma Morris (E)

Department of Hematology, University College Hospital NHS Trust; Cancer Institute UCL, London.

Kirsty Thomson (K)

Department of Hematology, University College Hospital NHS Trust, London.

Karl S Peggs (KS)

Department of Hematology, University College Hospital NHS Trust; Cancer Institute UCL, London.

Ronjon Chakraverty (R)

Department of Hematology, University College Hospital NHS Trust; Cancer Institute UCL, London.

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Classifications MeSH