ASTCT, CIBMTR, and EBMT clinical practice recommendations for transplant and cellular therapies in mantle cell lymphoma.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
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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
Аннотация
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.