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ASTCT, CIBMTR, and EBMT clinical practice recommendations for transplant and cellular therapies in mantle cell lymphoma

Authors :
Munshi, Pashna N.
Hamadani, Mehdi
Kumar, Ambuj
Dreger, Peter
Friedberg, Jonathan W.
Dreyling, Martin
Kahl, Brad
Jerkeman, Mats
Kharfan-Dabaja, Mohamed A.
Locke, Frederick L.
Shadman, Mazyar
Hill, Brian T.
Ahmed, Sairah
Herrera, Alex F.
Sauter, Craig S.
Bachanova, Veronika
Ghosh, Nilanjan
Lunning, Matthew
Kenkre, Vaishalee P.
Aljurf, Mahmoud
Wang, Michael
Maddocks, Kami J.
Leonard, John P.
Kamdar, Manali
Phillips, Tycel
Cashen, Amanda F.
Inwards, David J.
Sureda, Anna
Cohen, Jonathon B.
Smith, Sonali M.
Carlo-Stella, Carmello
Savani, Bipin
Robinson, Stephen P.
Fenske, Timothy S.
Source :
Bone Marrow Transplantation; 20240101, Issue: Preprints p1-11, 11p
Publication Year :
2024

Abstract

Autologous (auto-) or allogeneic (allo-) hematopoietic cell transplantation (HCT) are accepted treatment modalities for mantle cell lymphoma (MCL). Recently, chimeric antigen receptor (CAR) T-cell therapy received approval for MCL; however, its exact place and sequence in relation to HCT is unclear. The ASTCT, CIBMTR, and the EBMT, jointly convened an expert panel to formulate consensus recommendations for role, timing, and sequencing of auto-, allo-HCT, and CAR T-cell therapy for patients with newly diagnosed and relapsed/refractory (R/R) MCL. The RAND-modified Delphi method was used to generate consensus statements. Seventeen consensus statements were generated; in the first-line setting auto-HCT consolidation represents standard-of-care in eligible patients, whereas there is no clear role of allo-HCT or CAR T-cell therapy, outside of a clinical trial. In the R/R setting, the preferential option is CAR T-cell therapy especially in MCL failing or intolerant to at least one Bruton’s tyrosine kinase inhibitor, while allo-HCT is recommended if CAR T-cell therapy has failed or is not feasible. In the absence of contemporary evidence-based data, the panel found RAND-modified Delphi methodology effective in providing a formal framework for developing consensus recommendations for the timing and sequence of cellular therapies for MCL.

Details

Language :
English
ISSN :
02683369 and 14765365
Issue :
Preprints
Database :
Supplemental Index
Journal :
Bone Marrow Transplantation
Publication Type :
Periodical
Accession number :
ejs57471899
Full Text :
https://doi.org/10.1038/s41409-021-01288-9