TY - JOUR
T1 - Carfilzomib, lenalidomide, dexamethasone (KRD) in BTKi relapsed or refractory mantle cell lymphoma: A phase II study from Fondazione Italiana Linfomi
AU - Cavallo, Federica
AU - Clerico, Michele
AU - Lucchini, Elisa
AU - Castiglione, Anna
AU - Re, Alessandro
AU - Zilioli, Vittorio Ruggiero
AU - Visco, Carlo
AU - Tani, Monica
AU - Olivieri, Jacopo
AU - Arcaini, Luca
AU - Fabbri, Alberto
AU - GAIDANO, Gianluca
AU - Dodero, Anna
AU - Zaja, Francesco
PY - 2024
Y1 - 2024
N2 - Mantle cell lymphoma (MCL) is a rare lymphoproliferative neoplasm considered incurable, with a median survival of 3–5 years. In recent years, Bruton's tyrosine kinase inhibitors (BTKi) have been introduced, demonstrating high therapeutic activity. However, the prognosis for MCL patients failing ibrutinib therapy is particularly poor, with a survival expectation of a few months. In this phase II trial, we assessed the efficacy and safety of the carfilzomib-lenalidomide-dexamethasone (KRD) combination in MCL patients who were relapsed/refractory (R/R) or intolerant to BTKi and in need of treatment. The primary objective of the study was to evaluate the antitumor efficacy of the KRD combination in terms of 12-month overall survival (12-month OS). From September 2019 to December 2020, 16 patients were enrolled from 11 Italian centers. After a median follow-up of 2.37 months (95% CI 0.92–6.47), the 12-month OS was 13%. The rate of grade 3–4 adverse events (AEs) was 35%, and the overall response rate (ORR) was 19%. These results led to the premature termination of enrollment, as defined in the protocol stopping rules. The efficacy of the KRD combination in advanced-stage MCL patients who are R/R to BTKi is unsatisfactory and too toxic.
AB - Mantle cell lymphoma (MCL) is a rare lymphoproliferative neoplasm considered incurable, with a median survival of 3–5 years. In recent years, Bruton's tyrosine kinase inhibitors (BTKi) have been introduced, demonstrating high therapeutic activity. However, the prognosis for MCL patients failing ibrutinib therapy is particularly poor, with a survival expectation of a few months. In this phase II trial, we assessed the efficacy and safety of the carfilzomib-lenalidomide-dexamethasone (KRD) combination in MCL patients who were relapsed/refractory (R/R) or intolerant to BTKi and in need of treatment. The primary objective of the study was to evaluate the antitumor efficacy of the KRD combination in terms of 12-month overall survival (12-month OS). From September 2019 to December 2020, 16 patients were enrolled from 11 Italian centers. After a median follow-up of 2.37 months (95% CI 0.92–6.47), the 12-month OS was 13%. The rate of grade 3–4 adverse events (AEs) was 35%, and the overall response rate (ORR) was 19%. These results led to the premature termination of enrollment, as defined in the protocol stopping rules. The efficacy of the KRD combination in advanced-stage MCL patients who are R/R to BTKi is unsatisfactory and too toxic.
KW - carfilzomib
KW - clinical haematology
KW - lenalidomide
KW - mantle cell lymphoma
KW - carfilzomib
KW - clinical haematology
KW - lenalidomide
KW - mantle cell lymphoma
UR - https://iris.uniupo.it/handle/11579/202415
U2 - 10.1111/bjh.19617
DO - 10.1111/bjh.19617
M3 - Article
SN - 0007-1048
VL - 205
SP - 1404
EP - 1410
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 4
ER -