TY - JOUR
T1 - A multicenter retrospective comparison of induction chemoimmunotherapy regimens on outcomes in transplant-eligible patients with previously untreated mantle cell lymphoma
AU - Ng, Zi Yun
AU - Bishton, Mark
AU - Ritchie, David
AU - Campbell, Robert
AU - Gilbertson, Michael
AU - Hill, Kate
AU - Ratnasingam, Sumita
AU - Schwarer, Anthony
AU - Manos, Kate
AU - Shorten, Sophie
AU - Ng, Melissa
AU - Nelson, Niles
AU - Xin, Liu
AU - De Mel Widanalage, Sanjay
AU - Sunny, Tenny
AU - Purtill, Duncan
AU - Poon, Michelle
AU - Johnston, Anna
AU - Cochrane, Tara
AU - Lee, Hui Peng
AU - Hapgood, Greg
AU - Tam, Constantine
AU - Opat, Stephen
AU - Hawkes, Eliza
AU - Seymour, John
AU - Cheah, Chan Yoon
PY - 2019/8
Y1 - 2019/8
N2 - Mantle cell lymphoma (MCL) is an uncommon and typically aggressive form of lymphoma. Although often initially chemosensitive, relapse is common. Several induction and conditioning regimens are used in transplant-eligible patients, and the optimal approach remains unknown. We performed an international, retrospective study of transplant-eligible patients to assess impact of induction chemoimmunotherapy and conditioning regimens on clinical outcomes. We identified 228 patients meeting inclusion criteria. Baseline characteristics were similar among the induction groups except for some variation in age. The type of induction chemoimmunotherapy received did not influence overall response rates (ORRs) (0.43), progression-free survival (PFS) (P >.67), or overall survival (OS) (P >.35) on multivariate analysis (PFS and OS). Delivery of autologous stem cell transplant (ASCT) was associated with favorable PFS and OS (0.01) on univariate analysis only; this benefit was not seen on multivariate analysis—PFS (0.36) and OS (0.21). Compared with busulfan and melphalan (BuMel), the use of the carmustine, etoposide, cytarabine, melphalan (BEAM)–conditioning regimen was associated with inferior PFS (HR = 2.0 [95% CI 1.1-3.6], 0.02) but not OS (HR = 1.1 [95% CI 0.5-2.3], 0.81) on univariate analysis only. Within the limits of a retrospective study and modest power for some comparisons, type of induction therapy did not influence ORR, PFS, or OS for transplant-eligible patients with MCL. International efforts are required to perform randomized clinical trials evaluating chemoimmunotherapy induction regimens.
AB - Mantle cell lymphoma (MCL) is an uncommon and typically aggressive form of lymphoma. Although often initially chemosensitive, relapse is common. Several induction and conditioning regimens are used in transplant-eligible patients, and the optimal approach remains unknown. We performed an international, retrospective study of transplant-eligible patients to assess impact of induction chemoimmunotherapy and conditioning regimens on clinical outcomes. We identified 228 patients meeting inclusion criteria. Baseline characteristics were similar among the induction groups except for some variation in age. The type of induction chemoimmunotherapy received did not influence overall response rates (ORRs) (0.43), progression-free survival (PFS) (P >.67), or overall survival (OS) (P >.35) on multivariate analysis (PFS and OS). Delivery of autologous stem cell transplant (ASCT) was associated with favorable PFS and OS (0.01) on univariate analysis only; this benefit was not seen on multivariate analysis—PFS (0.36) and OS (0.21). Compared with busulfan and melphalan (BuMel), the use of the carmustine, etoposide, cytarabine, melphalan (BEAM)–conditioning regimen was associated with inferior PFS (HR = 2.0 [95% CI 1.1-3.6], 0.02) but not OS (HR = 1.1 [95% CI 0.5-2.3], 0.81) on univariate analysis only. Within the limits of a retrospective study and modest power for some comparisons, type of induction therapy did not influence ORR, PFS, or OS for transplant-eligible patients with MCL. International efforts are required to perform randomized clinical trials evaluating chemoimmunotherapy induction regimens.
KW - autologous stem cell transplant
KW - conditioning
KW - induction
KW - mantle cell lymphoma
UR - https://www.scopus.com/pages/publications/85066894068
U2 - 10.1002/hon.2618
DO - 10.1002/hon.2618
M3 - Article
C2 - 30983008
AN - SCOPUS:85066894068
SN - 0278-0232
VL - 37
SP - 253
EP - 260
JO - Hematological Oncology
JF - Hematological Oncology
IS - 3
ER -