TY - JOUR
T1 - ASTCT, CIBMTR, and EBMT clinical practice recommendations for transplant and cellular therapies in mantle cell lymphoma
AU - Munshi, Pashna N.
AU - Hamadani, Mehdi
AU - Kumar, Ambuj
AU - Dreger, Peter
AU - Friedberg, Jonathan W.
AU - Dreyling, Martin
AU - Kahl, Brad
AU - Jerkeman, Mats
AU - Kharfan-Dabaja, Mohamed A.
AU - Locke, Frederick L.
AU - Shadman, Mazyar
AU - Hill, Brian T.
AU - Ahmed, Sairah
AU - Herrera, Alex F.
AU - Sauter, Craig S.
AU - Bachanova, Veronika
AU - Ghosh, Nilanjan
AU - Lunning, Matthew
AU - Kenkre, Vaishalee P.
AU - Aljurf, Mahmoud
AU - Wang, Michael
AU - Maddocks, Kami J.
AU - Leonard, John P.
AU - Kamdar, Manali
AU - Phillips, Tycel
AU - Cashen, Amanda F.
AU - Inwards, David J.
AU - Sureda, Anna
AU - Cohen, Jonathon B.
AU - Smith, Sonali M.
AU - Carlo-Stella, Carmello
AU - Savani, Bipin
AU - Robinson, Stephen P.
AU - Fenske, Timothy S.
N1 - Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12
Y1 - 2021/12
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85113212083&partnerID=8YFLogxK
U2 - 10.1038/s41409-021-01288-9
DO - 10.1038/s41409-021-01288-9
M3 - Article
C2 - 34413469
AN - SCOPUS:85113212083
SN - 0268-3369
VL - 56
SP - 2911
EP - 2921
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 12
ER -